Bibliografia - Rasy psów i kotów. Przewodnik weterynaryjny by Wydawnictwo Galaktyka

ISBN: 978-83-7579-288-1

RASY PSÓW I KOTÓW

Z tej książki dowiesz się: • jak rozpoznawać i leczyć choroby związane z rasą u psów i kotów • jakie badania genetyczne należy wykonać, aby zdiagnozować wadę genetyczną lub podjąć decyzję o dopuszczeniu danego zwierzęcia do rozrodu • jakie są charakterystyczne cechy poszczególnych ras i do jakich chorób wykazują one predyspozycje • jak podejmować odpowiednie decyzje hodowlane, które przyczynią się do poprawy zdrowia całej linii i rasy zwierząt

PRZEWODNIK WETERYNARYJNY

prof. dr hab. Roman Lechowski

Jerold S. Bell Kathleen E. Cavanagh Larry P. Tilley Francis W.K. Smith

Książka Rasy psów i kotów – przewodnik weterynaryjny jest pozycją unikatową nie tylko na polskim, ale także na światowym rynku literatury weterynaryjnej. Po raz pierwszy w całościowy i nowoczesny sposób przedstawiono zwięzłe i wyczerpujące informacje kynologiczne i felinologiczne oraz dotyczące predylekcji rasowych do określonych chorób u poszczególnych ras psów i kotów. Dokładny opis ras psów i kotów, poparty najnowszą wiedzą na temat uwarunkowań genetycznych i predyspozycji do danych chorób, sprawia, że ten podręcznik powinien się znaleźć w bibliotece każdego lekarza weterynarii. Szczególną wartość praktyczną mają informacje dotyczące dostępności badań genetycznych dla swoistych chorób związanych z rasą psa lub kota. Warto podkreślić, że książka jest bardzo przyjazna dla czytelnika. Odnalezienie potrzebnych wiadomości ułatwia alfabetyczny układ opisów ras oraz tabelaryczne zestawienie predylekcji do określonych chorób. Korzystam z tego podręcznika bardzo często – niekiedy nawet kilka razy dziennie. Cieszę się, że jest już dostępny w polskim tłumaczeniu. Polecam go wszystkim lekarzom weterynarii zajmującym się psami i kotami, studentom oraz hodowcom.

RASY PSÓW I KOTÓW PRZEWODNIK WETERYNARYJNY Charakterystki ras • Predylekcje do chorób Wskazania diagnostyczne i terapeutyczne 171 ras psów, 42 rasy kotów

Jerold S. Bell, Kathleen E. Cavanagh, Larry P. Tilley, Francis W.K. Smith

rasy ps贸w

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Airedale terier

Akita inu 1. Fujise H., Higa K., Nakayama T. et al., Incidence of dogs possessing red blood cells with high K in Japan and East Asia, J Vet Med Sci, June 1997, 59(6):495– 497. 2. Degen M., Pseudohyperkalemia in Akitas, J Am Vet Med Assoc, March (1) 1987, 190(5):541–543. 3. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 4. Dorn C.R., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals, Monograph, AKC Caninte Health Foundation, 2000. 5. LaFond E., Breur G., Austin C., Breed susceptibility for developmental orthopedic diseases in dogs, J Am Anim Hosp Assoc, September–October 2002, 38(5):467–477. 6. Glickman L., Glickman N., Raghaven M., The Akita Club of America National Health Survey 2000–2001, 2001. 7. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April 2007. 8. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs hypothyroidism, J Am Vet Med Assoc, February 15 2002, 220(4), s. 466–471. 9. Glickman L., Glickman N., Schellenberg D. et al., Incidence of and breed-related risk factors for gastric dilatation-volvulus in dogs, J Am Vet Med Assoc, January (1) 2000, 216(1):40–45. 10. Duval J., Budsberg S., Flo G. et al., Breed, sex, and body weight as risk factors for rupture of the cranial cruciate ligament in young dogs, J Am Vet Med Assoc, September (15) 1999, 215(6):811–814. 11. Reichler I., Hauser B., Schiller I. et al., Sebaceous adenitis in the Akita: clinical observations, histopathology and heredity, Vet Dermatol, October 2001, 12(50):243–253. 12. White S.D., Rosychuk R.A., Scott K.V. et al., Sebaceous adenitis in dogs and results of treatment with isotretinoin and etretinate: 30 cases (1990–1994), J Am Vet Med Assoc, July (15) 1995, 207(2):197–200. 13. Hernblad Tevell E., Bergvall K., Egenvall A., Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases, Acta Vet Scand, May (25) 2008, 50(1):11. 14. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 15. Angles J.M., Famula T.R., Pedersen N.C. et al., Uveodermatologic (VKH-like) syndrome in American Akita dogs is associated with an increased frequency of DQA1*00201, Tissue Antigens, December 2005, 66(6):656–665.

16. Cottrell B.D., Barnett K.C., Harada disease in the Japanese Akita, J Small Anim Pract 1987, 28:517. 17. Murphy C.J., Bellhorn R.W., Anti-retinal antibodies associated with Vogt-Koyanagi-Harada-like syndrome in a dog, J Am Anim Hosp Assoc 1991, 27:399. 18. Kuhl K.A., Shofer F.S., Goldschmidt M.H., Comparative histopathology of pemphigus foliaceus and superficial folliculitis in the dog, Vet Pathol, January 1994, 31(1):19–27. 19. Ihrke P.J., Stannard A.A., Ardans A.A. et al., Pemphigus foliaceus in dogs: a review of 37 cases, J Am Vet Med Assoc, January (1) 1985, 186(1):59–66. 20. Shelton G.D., Schule A., Kass P.H., Risk factors for acquired myasthenia gravis in dogs: 1,154 cases (1991–1995), J Am Vet Med Assoc, December (1) 1997, 211(11):1428– 1431. 21. Dougherty S.A., Center S.A., Shaw E.E. et al., Juvenile-onset polyarthritis syndrome in Akitas, J Am Vet Med Assoc, March (1) 1991, 198(5):849–856. 22. Gelatt K.N., MacKay E.O., Prevalence of the breed-related glaucomas in pure-bred dogs in North America, Vet Ophthalmol 2004 March-April, 7(2):97–111. 23. O’Toole D., Roberts S., Generalized progressive retinal atrophy in two Akita dogs, Vet Pathol, September 1984, 21(5):457–62; December (1) 1997, 211(11):1428–1431. 24. Paulsen M.E., Severin G.A., Young S. et al., Progressive retinal atrophy in a colony of Akita dogs, Trans Am Col Vet Ophthalmol 1988, 19:1–4. 25. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press 1999, s. 195. 26. Laratta L.J., Riis R.C., Kern T. et al., Multiple congenital ocular defects in the Akita dog, Cornell Vet, July 1985, 75(3):381–392. 27. Labelle P., Roy M., Mohr F., Primary diffuse tracheobronchial amyloidosis in a dog, J Comp Pathol, November 2004, 131(4):338–340. 28. Hashizume C.T., Cervical spinal arachnoid cyst in a dog, Can Vet J, March 2000, 41(3):225–227. 29. Nagata M., Shimizu H., Masunaga T. et al., Dystrophic form of inherited epidermolysis bullosa in a dog (Akita Inu), Br J Dermatol, Dezember 1995, 133(6):1000–1003. 30. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 341–344.

Alaskan malamut 1. Lilliehook I., Tvedten H., Investigation of hypereosinophilia and potential treatments, Vet Clin North Am Small Anim Pract, November 2003; 33(6):1359–1378, VIII. 2. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 3. Fletch S., Smart M., Pennock P., Subden R., Clinical and pathologic features of chondrodysplasia (dwarfism) in the Alaskan Malamute, J Am Vet Med Assoc, March 1973; 162(5):357–361. 4. Subden R., Fletch S., Smart M. et al. Genetics of the Alaskan Malamute chondrodysplasia syndrome, Journal of Heredity, 1972, 63:149–152. 5. Braund K.G., Shores A., Lowrie C. et al., Idiopathic polyneuropathy in Alaskan malamutes, J Vet Intern Med, July-August 1997; 11(4):243–249. 6. Moe L., Hereditary polyneuropathy of Alaskan malamutes, [w:] Kirk R.W., Bonagura J.D. (eds), Current Veterinary

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26. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 232–236.

Amerykański pies eskimoski 1. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 2. Morris Animal Foundation, Morris Animal Foundation Update, Genetic Tests Focus on Breed-Specific Vision Problems, Canine Pract 1999, 24(4):21. 3. Moody J., Famula T. et al., Identification of microsatellite markers linked to progressive retinal atrophy in American Eskimo Dogs, AJVR 2005, 66(11):1900–1902. 4. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 5. Strain G., Deafness prevalence and pigmentation and gender associations in dog breeds at risk, Vet J, January 2004; 167(1):23. 6. Giger U., Regenerative anemias caused by blood loss or hemolysis, [w:]Ettinger S.J., Feldman E.C. (eds.), Textbook of Veterinary Internal Medicine, Philadelphia: Saunders 2000, s.1784–1804. 7. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 8. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002;220(4),466–471. 9. Dorn C., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals., Monograph, AKC Caninte Health Foundation, 2000. 10. Chastain C., Sex Hormone Concentrations in Dogs with Alopecia, Sm Anim Clin Endocrinol, 2004, 14(1):37–38. 11. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 196. 12. Lees G., Update: Inherited Primary Glomerular Diseases in Dogs, Proceedings ACVIM Forum, 2003. 13. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 525–528. 14. Awano T., Johnson G., Wade C. et al., Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis, Proc Natl Acad Sci USA, February 2009, 106(8):2794–2799.

Amerykański spaniel wodny 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 3. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 4. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 15; 220(4),466–471. 5. Coates J., Zeng R., Awano T. et al., An SOD1 Mutation Associated with Degenerative Myelopathy Occurs in Many

Dog Breeds, Proceedings 2009 ACVIM Forum, 2009. 6. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 197. 7. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 76–78.

Amerykański staffordshire terrier 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Olby N., Blot S., Thibaud J. et al., Cerebellar cortical degeneration in adult American Staffordshire Terriers, J Vet Intern Med, March-April 2004, 18(2):201–208. 3. Siso S., Navarro C., Hanzlicek D. et al., Adult onset thalamocerebellar degeneration in dogs associated to neuronal storage of ceroid lipopigment, Acta Neuropathol (Berl), November 2004, 108(5):386–392. 4. Hanzlicek D., Kathmann I., Bley T. et al., Cerebellar cortical abiotrophy in American Staffordshire terriers: clinical and pathological description of 3 cases, Schweiz Arch Tierheilkd, August 2003, 145(8):369–375. 5. Abitbol M., Thibaud J., Olby N. et al., Identification of a Single Point Mutation Strongly Associated With the Cerebellar Cortical Abiotrophy of the American Staffordshire Terrier, Proceedings, 2009 ACVIM Conference, 2009. 6. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 7. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 15;220(4),466–471. 8. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 9. Duval J., Budsberg S., Flo G. et al., Breed, sex, and body weight as risk factors for rupture of the cranial cruciate ligament in young dogs, J Am Vet Med Assoc, September 1999, 215(6):811–814. 10. Akhmedov N., Baldwin V., Zangerl B. et al., Cloning and characterization of the canine photoreceptor specific conerod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog, Mol Vis, March 2002, 8:79–84. 11. Costa S., Munhoz T., Calazans S. et al., Clinical and Epidemiological Evaluation of Actinic Keratosis in Seven Dogs, Proceedings, 2009 WSAVA World Congress, 2009. 12. Gualtieri M., Monzeglio M., Scanziani E., Gastric neoplasia, Vet Clin North Am Small Anim Pract, March 1999, 29(2):415–440. 13. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 196–197. 14. Nowacka J., Nizanski W., Klimowicz M. et al., Lack of the SOX9 Gene Polymorphism in Sex Reversal Dogs (78, XX; SRY negative), J Hered, November-December 2005, 96(7):797–802. 15. Romanucci M., Malatesta D., Guardiani P. et al., Xanthogranu-lomatous inflammation of the small bowel in a dog, Vet Pathol, March 2008, 45(2):207–211. 16. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 345–347.

17. Karmi N., Brown E., Hughes S. et al., Estimated frequency of the canine hyperuricosuria mutation in different dog breeds, J Vet Intern Med, November-December 2010, 24(6):1337–1342.

Anatolijski pies pasterski 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 3. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 15;220(4),466–471. 4. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 5. Temizsoylu M., Avki S., Complete ventral ankyloglossia in three related dogs, J Am Vet Med Assoc, November 2003, 223(10):1443–1445, 1433. 6. Grundmann S., Hofmann A., Ankyloglossia in an Anatolian Shepherd dog, Schweiz Arch Tierheilkd, August 2006, 148(8):417–420. 7. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 197. 8. Bosje J., van den Ingh T., Fennema A. et al., Copper-induced hepatitis in an Anatolian shepherd dog, Vet Rec, January 2003, 152(3):84–85. 9. Haziroglu R., Kul O., Tunca R. et al., Osteoclast-like giant cell tumour arising from the kidney in a dog, Acta Vet Hung, 2005, 53(2):225–230. 10. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 237–239.

Australijski pies pasterski 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Dorn C., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals., Monograph, AKC Caninte Health Foundation, 2000. 3. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 4. Collier L., McCalla T., Moor C., Anterior lens luxation in Queensland Heeler (Australian Cattle) dogs, Proc Am Coll Vet Ophthal 1989, 20:18. 5. Johnsen D., Maggs D., Kass P., Evaluation of risk factors for development of secondary glaucoma in dogs: 156 cases (1999–2004), J Am Vet Med Assoc, October 2006, 229(8):1270–1274. 6. Brenner O., de Lahunta A., Summers B. et al., Hereditary polioencepha-lomyelopathy of the Australian Cattle Dog, Acta Neuropath, July 1997, 94(1):54–66. 7. Harkin K., Goggin J., DeBey B. et al., Magnetic Resonance imaging of 37 the brain of a dog with hereditary polioencephalomyopathy, J Am Vet Med Assoc, May 1999, 214(9):1342–1344. 8. Li F., Cuddon P., Song J., Wood S. et al., Canine spongiform leukoencephalomyelopathy is associated with a missense mutation in cytochrome b, Neurobiol Dis, July 2005.

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8. 9. 10. 11. 12. 13. 14. 15. 16.

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Norweski lundehund 1. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 2. Berghoff N., Ruaux C., Steiner J. et al., Gastroenteropathy in Norwegian Lundehunds, Compend Contin Educ Vet, August 2007, 29(8):456–465, 468–470; quiz 470–471. 3. Landsverk T., Gamlem H., Intestinal lymphangiectasia in the Lundehund. Scanning electron microscopy of intestinal mucosa, Acta Pathol Microbiol Immunol Scand A, September 1984, 92(5):353–362. 4. Kolbjørnsen O., Press C., Landsverk T., Gastropathies in the Lundehund. I. Gastritis and gastric neoplasia associated with intestinal lymphangiectasia, APMIS, September 1994, 102(9):647–661. 5. Flesjå K., Yri T., Protein-losing enteropathy in the Lundehund, J Small Anim Pract, January 1977, 18(1):11–23. 6. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 7. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 8. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 9. Qvigstad G., Kolbjørnsen Ø., Skancke E. et al., Gastric neuroendocrine carcinoma associated with atrophic gastritis in the norwegian lundehund, J Comp Pathol, November 2008, 139(4):194–201. 10. Strona rasy na portalu AKC: www.akc.org/breeds/norwegian_lundehund Dostęp: 1 lipca 2010.

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5. Ketring K., Schirmer Testing & Tonometry Are „Good Medicine”, Proceedings, 2005 Western Veterinary Conference, 2005. 6. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 7. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 8. Center S., Portosystemic Vascular Anomalies & Hepatic MVD: Evidence of Common Genetics in Small Dogs, Proceedings, 2008 ACVIM Forum, 2008. 9. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 229. 10. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 412–413.

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Owczarek australijski 1. Clark L., Wahl J., Rees C. et al., Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog. Proc Natl Acad Sci USA, January 2006, 103(5):1376–1381. 2. Hedan B., Corre S., Hitte C. et al., Coat colour in dogs: identification of the merle locus in the Australian shepherd breed, BMC Vet Res, February 2006,2:9. 3. Geyer J., Doring B., Godoy J. et al., Development of a PCR-based diagnostic test detecting a nt230(del4) MDR1 mutation in dogs: verification in a moxidectin-sensitive Australian Shepherd, J Vet Pharmacol Ther, February 2005, 28(1):95–99. 4. Nelson O., Carsten E., Bentjen S. et al., Ivermectin toxicity in an Australian Shepherd dog with the MDR1 mutation associated with ivermectin sensitivity in Collies, J Vet Intern Med, May-June 2003, 17(3):354–356. 5. Geyer J., Doring B., Godoy J. et al., Frequency of the nt230 (del4) MDR1 mutation in Collies and related dog breeds in Germany, J Vet Pharmacol Ther, 2005 December, 28(6):545–551. 6. Neff M., Robertson K., Wong A. et al., Breed distribution and history of canine mdr1-1Delta, a pharmacogenetic mutation that marks the emergence of breeds from the collie lineage, Proc Natl Acad Sci USA, August 2004, 101(32):11725–11730. 7. Mealey K., Meurs K., Breed distribution of the ABCB1-1Delta (multidrug sensitivity) polymorphism among dogs undergoing ABCB1 genotyping, J Am Vet Med Assoc, September 2008, 233(6):921–924.

8. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 9. LaFond E., Breur G., Austin C., Breed susceptibility for developmental orthopedic diseases in dogs, J Am Anim Hosp Assoc, September-October 2002, 38(5):467–477. 10. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 11. Mellersh C., Pettitt L., Forman O. et al., Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts, Vet Ophthalmol, September-October 2006, 9(5):369–378. 12. Mellersh C., McLaughlin B., Ahonen S. et al., Mutation in HSF4 is associated with hereditary cataract in the Australian Shepherd, Vet Ophthalmol, November-December 2009, 12(6):372–378. 13. Lowe J., Kukekova A., Kirkness E. et al., Linkage mapping of the primary disease locus for collie eye anomaly, Genomics, July 2003, 82(1):86–95. 14. Munyard K., Sherry C., Sherry L., A retrospective evaluation of congenital ocular defects in Australian Shepherd dogs in Australia, Vet Ophthalmol, January-February 2007, 10(1):19–22. 15. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 16. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 15;220(4),466–471. 17. Strain G. Deafness prevalence and pigmentation and gender associations in dog breeds at risk, The Veterinary Journal 2004, 167(1):23–32. 18. Strain G., Clark L., Wahl J. et al., Prevalence of deafness in dogs heterozygous or homozygous for the merle allele, J Vet Intern Med, March-April 2009, 23(2):282–286. 19. Sharp C., Adolphson P., Results of the 1999 ASCA Breed Health Survey, Aussie Times, January-February 2002. 20. Chavkin M., Roberts S., Salman M. et al., Risk factors for development of chronic superficial keratitis in dogs, J Am Vet Med Assoc, May 1994, 204(10):1630–1634. 21. Case L., Ling G., Franti C. et al., Cystine-containing urinary calculi in dogs: 102 cases (1981-1989), J Am Vet Med Assoc, July 1992, 201(1):129–133. 22. Gelatt K., Powell N., Huston K., Inheritance of microphthalmia with coloboma in the Australian shepherd dog, Am J Vet Res, October 1981, 42(10):1686–1690. 23. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 198. 24. He Q., Madsen M., Kilkenney A. et al., Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo, Blood, August 2005, 106(4):1447–1453. 25. O’Brien D., Katz M., Neuronal ceroid lipofuscinosis in 3 Australian shepherd littermates, J Vet Intern Med, March-April 2008, 22(2):472–475. 26. De Cock H., Busch M., Fry M. et al., A peripheral primitive neuroectodermal tumor with generalized bone metastases in a puppy, Vet Pathol, July 2004, 41(4):437–441. 27. Shelton G., Sammut V., Homma S. et al., Myofibrillar myopathy with desmin accumulation in a young Australian Shepherd dog, Neuromuscul Disord, July 2004, 14(7):399–404.

28. Sponenberg D., Bowling A., Heritable syndrome of skeletal defects in a family of Australian shepherd dogs, J Hered, September-October 1985, 76(5):393–394. 29. Lees G., Sautter J, Anemia and osteopetrosis in a dog. J Am Vet Med Assoc, October 1979, 175(8):820–824. 30. The Complete Dog Book, ed. 20, The American Kennel Club, Howell Book House: NY 2006, s. 612–615. 31. Karmi N., Brown E., Hughes S. et al., Estimated frequency of the canine hyperuricosuria mutation in different dog breeds, J Vet Intern Med, November-December 2010, 24(6):1337–1342.

Owczarek belgijski 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO 2007. 3. Miller T., Generalized Retinopathy in the Belgian Sheepdog, Invest Ophthalmol Vis Sci, 1986, 27(suppl.):310. 4. Wolf E., Samuelson D., Retinopathy in a family of Belgium shepherds, Proc American College of Veterinary Ophthalmologists, 1981, 12:supplement, 1981. 5. Dell’Osso L., Hertle R., Williams R. et al., A new surgery for congenital nystagmus: effects of tenotomy on an achiasmatic canine and the role of extraocular proprioception, J AAPOS, 1999. 6. Dell’Osso L., Williams R., Jacobs J. et al., The congenital and see-saw nystagmus in the prototypical achiasma of canines: comparison to the human achiasmatic prototype, Vision Res, June 1998, 38(11):1629–1641. 7. Hogan D., Williams R., Analysis of the retinas and optic nerves of achiasmatic Belgian sheepdogs, J Comp Neurol, February 1995. 8. Oberbauer A., Grossman D., Irion D. et al., The genetics of epilepsy in the Belgian tervuren and sheepdog, J Hered, January-February 2003, 94(1):57–63. 9. Berendt M., Gullřv C., Fredholm M., Focal epilepsy in the Belgian shepherd: evidence for simple Mendelian inheritance, J Small Anim Pract, December 2009, 50(12):655–661. 10. Berendt M., Gullřv C., Christensen S. et al., Prevalence and characteristics of epilepsy in the Belgian shepherd variants Groenendael and Tervueren born in Denmark 1995-2004, Acta Vet Scand, December 2008, 50:51. 11. Oberbauer A., Belanger J., Grossman D. et al., Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs, BMC Genet, May 2010,11:35. 12. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 13. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 220(4):466–471. 14. Gualtieri M., Monzeglio M., Scanziani E., Gastric neoplasia, Vet Clin North Am Small Anim Prac, March 1999, 29(2):415–440. 15. Lubbes D., Mandigers P., Heuven H. et al., Incidence of gastric carcinoma in Dutch Tervueren shepherd dogs born between 1991 and 2002, Tijdschr Diergeneeskd, July-August 2009, 134(14-15):606–610.

16. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press 1999, s. 201–202. 17. Larocca R., Unilateral external and internal ophthalmoplegia caused by intracranial meningioma in a dog, Vet Ophthalmol 2000, 3(1):3–9. 18. Booth M., Bastianello S., Jiminez M. et al., Malignant fibrous histiocytoma of the deep peri-articular tissue of the stifle in a dog, J S Afr Vet Assoc, December 1998, 69(4):163–168. 19. Shelton G.D., Cardinet G.H. 3rd, Bandman E. et al. Fiber type-specific autoantibodies in a dog with eosinophilic myositis, Muscle Nerve, November-December 1985, 8(9):783–790. 20. Miller M., Pool R., Coolman B., Synovial hemangioma in the stifle joint of a dog, Vet Pathol, March 2007, 44(2):240–243. 21. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 624–628.

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Owczarek belgijski tervuren

Owczarek francuski beauceron

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Petit basset griffon vendéen 1. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 2. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 3. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 4. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 5. Petit Basset Griffon Vendéen Club of America, 2000 PBGV Health Survey, 2000. 6. Chaudidu G., Clerc B. et al., Primary Lens Luxation in the Petite Bassett Griffon Vendeen in France, ECVO Proceedings, 2002. 7. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 231. 8. Nicolle A.P., Carlos Sampedrano C., Fontaine J.J. et al., Longitudinal left ventricular myocardial dysfunction assessed by 2D colour tissue Doppler imaging in a dog with systemic hypertension and severe arteriosclerosis, J Vet Med A Physiol Pathol Clin Med, March 2005, 52(2):83–87. 9. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 200–204.

Pies faraona 1. Kintzer P.P., Peterson M.E., Progress in the Diagnosis and Treatment of Canine Hypothyroidism, Proceedings, ACVIM 2007, 2007. 2. Court M.H., Anesthesia of the sighthound, Clin Tech Small Anim Pract, February 1999, 14(1):38–43. 3. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 4. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clini-

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cal signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 231-232. Campbell G.A., Crow D., Severe zinc responsive dermatosis in a litter of Pharaoh Hounds, J Vet Diagn Invest, July 2010, 22(4):663–666. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 205–208.

Pies pasterski z Entlebuch 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 3. Zangerl B., Goldstein O., Philp A. et al., Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans, Genomics, November 2006, 88(5):551–563. 4. Heitmann M., Hamann H., Brahm R. et al., Analysis of prevalence of presumed inherited eye diseases in Entlebucher Mountain Dogs, Vet Ophthalmol, May-June 2005, 8(3):145–151. 5. Müller C., Distl O., Association study of candidate genes for primary cataracts and fine-mapping of a candidate region on dog chromosome 1 in Entlebucher mountain dogs, Mol Vis, 16 May 2008, 14:883–888. 6. North C., Kruger J., Venta P. et al., Congenital Ureteral Ectopia in Continent and Incontinent-Related Entlebucher Mountain Dogs: 13 Cases (2006-2009), J Vet Intern Med, September-October 2010, 24(5):1055–1062. 7. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 8. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 9. Spiess B., Inherited eye diseases in the Entlebucher mountain dog, Schweiz Arch Tierheilkd, 1994, 136(3):105–110. 10. Strona rasy na portalu AKC: www.akc.org/breeds/entlebucher_mountain_dog Dostęp: 1 lipca 2010.

Pinczer małpi 1. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 2. Ocular Disorders Presumed to be Inherited in Purebred Dogs, American College of Veterinary Ophthalmologists, ACVO, 2007. 3. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 4. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clini-

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cal signs of hypothyroidism, J Am Vet Med Assoc, February 2002, 15;220(4),466–471. Waldman L., Seasonal flank alopecia in affenpinschers, J Small Anim Pract, June 1995,36(6),271–273. White S.D., Update on Follicular Alopecias: “Pseudo-Endocrinopathies”,Proceedings, ACVIM Forum, 2005. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 193. Lieb A., Grooters A., Tyler J. et al., Tetraparesis due to vertebral physeal fracture in an adult dog with congenital hypothyroidism, J Small Anim Pract, August 1997,38(8),364–367. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 447–449.

Pinczer miniaturowy 1. Drögemüller C., Philipp U., Haase B. et al., A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs, J Hered, 2007, 98(5):468–473. 2. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 3. LaFond E., Breur G., Austin C, Breed susceptibility for developmental orthopedic diseases in dogs, J Am Anim Hosp Assoc, September-October 2002, 38(5):467–477. 4. Dorn C., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals, Monograph, AKC Canine Health Foundation, 2000. 5. Stark D., Luxating patella in miniature pinschers, Vet Rec, September (14) 1991, 129(11):251. 6. Neer T., Dial S., Pechman R. et al., Clinical vignette. Mucopolysac-charidosis VI in a miniature pinscher, J Vet Intern Med, November-December 1995, 9(6):429–433. 7. Wang P., Seng A., Huff A. et al., Mucopolysaccharidosis in Dogs and Cats: Clinical Signs to DNA Tests, Proceedings, 2005 Tufts’ Canine and Feline Breeding and Genetics Conference, 2005. 8. Foureman P., Berman L., Stieger K. et al., Mucopolysaccharidosis Type VI in Miniature Pinschers: Screening For the Mutation, Proceedings, 2004 ACVIM Forum, 2004. 9. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 10. Gelatt K., Mackay E., Prevalence of primary breed-related cataracts in the dog in North America, Vet Ophthalmol, March-April 2005, 8(2):101–111. 11. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 12. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 13. Kim J., Kang K., Sohn H. et al., Color-dilution alopecia in dogs, J Vet Sci, September 2005, 6(3):259–261. 14. Miller S., Hohenhaus A., Hale A., Case-control study of blood type, breed, sex, and bacteremia in dogs with immune-mediated hemolytic anemia, J Am Vet Med Assoc, January (15) 2004, 224(2):232–235. 15. Case L., Ling G., Franti C. et al., Cystine-containing urinary calculi in dogs: 102 cases (1981-1989), J Am Vet Med Assoc, July (1)1992, 201(1):129–133.

16. Tobias K., Rohrbach B., Association of breed with the diagnosis of congenital portosystemic shunts in dogs: 2,400 cases (1980-2002), J Am Vet Med Assoc, December (1) 2003, 223(11):1636–1639. 17. Scott-Moncrieff J., Canine and Feline Diabetes Mellitus I, Proceedings, 2009 Western Veterinary Conference, 2009. 18. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 228. 19. Nowacka J., Nizanski W., Klimowicz M. et al.,Lack of the SOX9 Gene Polymorphism in Sex Reversal Dogs (78,XX; SRY negative), J Hered, November-December 2005, 96(7):797–802. 20. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 488–490.

Pinczer średni 1. Philipp U., Hamann H., Mecklenburg L. et al., Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs, BMC Genet, 16 June 2005, 6:34. 2. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 3. Leppanen M., Martenson J., Maki K., Results of ophthalmologic screening examinations of German Pinschers in Finland – a retrospective study, Vet Ophthalmol, September 2001, 4(3):165–169. 4. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 5. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 6. Nachreiner R.F., Refsal K.R., Graham P.A. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, 15 February 2002, 220(4):466–471. 7. Menzel J., Distl O., Unusual vascular ring anomaly associated with a persistent right aortic arch and an aberrant left subclavian artery in German pinschers, Vet J, March 2011, 187(3):352–325. 8. Poth T., Breuer W., Walter B. et al., Disorders of sex development in the dog-Adoption of a new nomenclature and reclassification of reported cases, Anim Reprod Sci, September 2010, 121(3–4):197–207. 9. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 262–265.

Pirenejski pies górski 1. Evans K., Adams V., Proportion of litters of purebred dogs born by caesarean section, J Small Anim Pract, February 2010, 51(2):113–118. 2. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 3. Grahn B., Cullen C., Retinopathy of Great Pyrenees dogs: fluorescein angiography, light microscopy and transmitting and scanning electron microscopy, Vet Ophthalmol, September 2001, 4(3):191–199. 4. Grahn B., Philibert H., Cullen C. et al., Multifocal Retinopathy of Great Pyrenees Dogs, Vet Comp Ophthalmol, December 1998, 1(4):211–221.

5. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 6. GPCA Health Committee, 2004 GPCA Health Survey Report, February 2006. 7. Dorn C., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals, Monograph, AKC Canine Health Foundation, 2000. 8. LaFond E., Breur G., Austin C., Breed susceptibility for developmental orthopedic diseases in dogs, J Am Anim Hosp Assoc, September-October 2002, 38(5):467–477. 9. Boudreaux M., Lipscomb D., Clinical, biochemical, and molecular aspects of Glanzmann’s thrombasthenia in humans and dogs, Vet Pathol, May 2001, 38(3):249–260. 10. Lipscomb D., Bourne C., Boudreaux M., Two genetic defects in alphaIIb are associated with type I Glanzmann’s thrombasthenia in a Great Pyrenees dog: a 14-base insertion in exon 13 and a splicing defect of intron 13, Vet Pathol, November 2000, 37(6):581–588. 11. Bingel S., Sande R., Chondrodysplasia in five Great Pyrenees, J Am Vet Med Assoc, September (15) 1994, 205(6):845–848. 12. Nachreiner R.F., Refsal K.R., Graham P.A. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, 15 February 2002, 220(4):466–471. 13. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 14. Strain G., Deafness prevalence and pigmentation and gender associations in dog breeds at risk, Vet J, January 2004, 167(1):23–32. 15. Gabriel A., Poncelet L., Van Ham L. et al., Laryngeal paralysis-polyneu-ropathy complex in young related Pyrenean mountain dogs, J Small Anim Pract, March 2006, 47(3):144–149. 16. Golden J., Banknieder A., Bruestle M., Hemophilia in a Great Pyrenees, Mod Vet Pract, August 1980, 61(8):671– 674. 17. Fogh J., Fogh I., Inherited coagulation disorders, Vet Clin North Am Small Anim Pract, January 1988, 18(1):231– 243. 18. Olsen D., Salwei R., Surgical Correction of a Congenital Preputial and Penile Deformity in a Dog. J Am Anim Hosp Assoc, March-April 2001, 37(2):187–192. 19. Ramirez G., Espinosa de los Monteros A., Rodriguez F. et al., Left ventricular outflow tract-right atrial communication (Gerbode type defect) associated with bacterial endocarditis in a dog, Vet Pathol, September 2003, 40(5):579–582. 20. Franch J., Cesari J., Font J., Craniomandibular osteopathy in two Pyrenean mountain dogs, Vet Rec, April (25) 1998, 142(17):455–459. 21. Mitten R., Edwards G., Rishniw M., Diagnosis and management of cor triatriatum dexter in a Pyrenean mountain dog and an Akita Inu, Aust Vet J, March 2001, 79(3):177–180. 22. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 221. 23. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 276–280.

Plott hound 1. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 2. Spellacy E., Shull R., Constantopoulos G. et al., A canine model of human alpha-L-iduronidase deficiency, Proc Natl Acad Sci USA, October 1983, 80(19):6091–6095. 3. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 4. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 5. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 6. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 700–702.

Podenco z Ibizy 1. Kintzer P., Peterson M., Progress in the Diagnosis and Treatment of Canine Hypothyroidism, Proceedings, ACVIM 2007, 2007. 2. Court M., Anesthesia of the sighthound, Clin Tech Small Anim Pract, February 1999, 14(1):38–43. 3. OFA statystyki rasy: www.offa.org, dostęp: 1 lipca 2010. 4. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 5. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 6. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 7. Strain G., Deafness prevalence and pigmentation and gender associations in dog breeds at risk, The Veterinary Journal, 2004, 167(1):23–32. 8. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 223. 9. Trower N., White R., Lamb C., Arteriovenous fistula involving the prepuce of a dog, J Small Anim Pract, October 1997, 38(10):455–458. 10. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 184–187.

Pointer (pointer angielski) 1. Sisson D., Schaeffer D., Changes in linear dimensions of the heart, relative to body weight as measured by M-mode echocardiography in growing dogs, Am J Vet Res, 1991, 52:1591–1596. 2. Evans K.M., Adams V.J., Proportion of litters of purebred dogs born by caesarean section, J Small Anim Pract, February 2010, 51(2):113–118. 3. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 4. Cummings J.F., de Lahunta A., Braund K.G. et al., Hereditary sensory neuropathy. Nociceptive loss and acral mutilation in pointer dogs: canine hereditary sensory neuropathy, Am J Pathol, July 1983, 112(1):136–138.

5. Sillevis Smitt P.A., de Jong J.M., Animal models of amyotrophic lateral sclerosis and the spinal muscular atrophies, J Neurol Sci, July 1989, 91(3):231–258. 6. O’Brien D.P., Shibuya H., Zhou T., X-Linked Cerebellar Ataxia in English Pointer Dogs: Phenotype and Linkage Data, Proceedings, 1997 AKC Canine Health Foundation Canine Health Conference, 1997. 7. Coppens A.G., Gilbert-Gregory S., Steinberg S.A. et al., Inner ear histopathology in “nervous Pointer dogs” with severe hearing loss, Hear Res, February 2005, 200(1–2):51–62. 8. Steinberg S.A., Klein E., Killens R.L. et al., Inherited deafness among nervous pointer dogs, J Hered, January-February 1994, 85(1):56–59. 9. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 10. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 11. Dorn C.R., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals, Monograph, AKC Canine Health Foundation, 2000. 12. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 13. American Pointer Club, 2002 APC Health & Research Survey, 2002. 14. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 231. 15. Morrison W.B., Wilsman N.J., Fox L.E. et al., Primary ciliary dyskinesia in the dog, J Vet Intern Med, April-June 1987, 1(2):67–74. 16. Cantile C., Baroni M., Tartarelli C.L. et al., Intramedullary hemangioblastoma in a dog. Vet Pathol, January 2003, 40(1):91–94. 17. Rallis T.S., Tontis D.K., Soubasis N.H. et al., Immunohistochemical study of a granular cell tumor on the tongue of a dog, Vet Clin Pathol, 2001, 30(2):62–66. 18. Reese W.G., Newton J.E., Angel C. et al., Induced immobility in nervous and normal Pointer dogs, J Nerv Ment Dis, October 1982, 170(10):605–613. 19. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 20–23.

Polski owczarek nizinny 1. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 2. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 3. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 4. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 5. Wrigstad A., Nilsson S.E., Dubielzig R. et al., Neuronal ceroid lipofuscinosis in the Polish Owczarek Nizinny (PON) dog. A retinal study, Doc Ophthalmol, 1995, 91(1):33–47.

6. Narfstrom K., Wrigstad A., Clinical, electrophysiological, and morphological findings in a case of neuronal ceroid lipofuscinosis in the Polish Owczarek Nizinny (PON) dog, Vet Q, April 1995, 17 Suppl 1:S46. 7. Narfström K., Wrigstad A., Ekesten B. et al., Neuronal ceroid lipofuscinosis: clinical and morphologic findings in nine affected Polish Owczarek Nizinny (PON) dogs, Vet Ophthalmol, March-April 2007, 10(2):111–120. 8. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 231. 9. McConnell J.F., Platt S., Smith K.C., Magnetic resonance imaging findings of an intracranial medulloblastoma in a Polish Lowland Sheepdog, Vet Radiol Ultrasound, January-February 2004, 45(1):17–22. 10. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 680–683.

Portugalski pies wodny 1. Slater M., The 2005 Portuguese Water Dog Health Survey, 2010. 2. Parker H.G., Chase K., Cadieu E. et al., An insertion in the RSPO2 gene correlates with improper coat in the Portuguese water dog, J Hered, September-October 2010, 101(5):612–617. 3. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 4. Chase K., Lawler D.F., Adler F.R. et al., Bilaterally asymmetric effects of quantitative trait loci (QTLs): QTLs that affect laxity in the right versus left coxofemoral (hip) joints of the dog (Canis familiaris), Am J Med Genet A, January (30) 2004, 124(3):239–247. 5. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 6. Zangerl B., Goldstein O., Philp A.R. et al., Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans, Genomics, November 2006, 88(5):551–563. 7. Shell L.G., Potthoff A.I., Carithers R. et al., Neuronal-visceral GM1 gangliosidosis in Portuguese water dogs, J Vet Intern Med, January-March 1989, 3(1):1–7. 8. Wang Z.H., Zeng B., Shibuya H. et al., Isolation and characterization of the normal canine beta-galactosidase gene and its mutation in a dog model of GM1-gangliosidosis, J Inherit Metab Dis, September 2000, 23(6):593–606. 9. Peterson M.E., Kintzer P.P., Kass P.H., Pretreatment clinical and laboratory findings in dogs with hypoadrenocorticism: 225 cases (1979-1993), J Am Vet Med Assoc, Jan uary (1) 1996, 208(1):85–91. 10. Chase K., Sargan D., Miller K. et al., Understanding the genetics of autoimmune disease: two loci that regulate late onset Addison’s disease in Portuguese Water Dogs, Int J Immunogenet, June 2006, 33(3):179–184. 11. Oberbauer A.M., Bell J.S., Belanger J.M. et al., Genetic evaluation of Addison’s disease in the Portuguese Water Dog, BMC Vet Res, May (2) 2006, 2:15. 12. Alroy J., Rush J.E., Freeman L. et al., Inherited infantile dilated cardiomyopathy in dogs: genetic, clinical, biochemical, and morphologic findings, Am J Med Genet, November (6) 2000, 95(1):57–66.

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6. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 7. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 8. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 9. Cerundolo R., Lloyd D.H., Persechino A. et . al, Treatment of canine Alopecia X with trilostane, Vet Dermatol, October 2004, 15(5):285–293. 10. Schmeitzel L.P., Lothrop C.D. Jr., Hormonal abnormalities in Pomeranians with normal coat and in Pomeranians with growth hormone-responsive dermatosis, J Am Vet Med Assoc, November (15) 1990, 197(10):1333–1341. 11. Cerundolo R., Lloyd D.H., Vaessen M.M. et al., Alopecia in pomeranians and miniature poodles in association with high urinary corticoid:creatinine ratios and resistance to glucocorticoid feedback, Vet Rec, March (24) 2007, 160(12):393–397. 12. Petric A.D., Hozjan E., Blejec A., Chronic Valvular Disease, Proceedings, 17th ECVIM-CA Congress, 2007. 13. Axlund T.W., Managing the Hydrocephalic Patient: Medical and Surgical Options, Proceedings, 2004 Atlantic Coast Veterinary Conference, 2004. 14. Pedersen N.C., Vernau K., Dickinson P. et al., DLA Association in Various Toy Breeds with Immune Mediated Encephalopathies, Proceedings, 2009 Tufts’ Canine and Feline Breeding and Genetics Conference, 2009. 15. Matsuki N., Takahashi M., Yaegashi M. et al., Serial examinations of anti-GFAP autoantibodies in cerebrospinal fluids in canine necrotizing meningoencephalitis, J Vet Med Sci, January 2009, 71(1):99–100. 16. McCarthy R.J., Lewis D.D., Hosgood G., Atlantoaxial Subluxation in Dogs, Compend Contin Educ Pract Vet, 1995, 17(2):215–226. 17. Denny H.R., Gibbs C., Waterman A., Atlanto-axial subluxation in the dog : A review of thirty cases and an evaluation of treatment by lag screw fixation, J Small Anim Pract, 1988, 29(1):37–47. 18. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 231–232. 19. LeVine D.N., Zhou Y., Ghiloni R.J. et al., Hereditary 1,25-dihydroxyvitamin D-resistant rickets in a Pomeranian dog caused by a novel mutation in the vitamin D receptor gene, J Vet Intern Med, November-December 2009, 23(6):1278–1283. 20. Fine D.M., Eyster G.E., Anderson L.K. et al., Cyanosis and congenital methemoglobinemia in a puppy, J Am Anim Hosp Assoc, January-February 1999, 35(1):33–35. 21. van Herpen H., Voorhout G., Occipital dysplasia in a Pomeranian dog, Tijdschr Diergeneeskd, May (15) 1993, 118(10):327–328. 22. Itoh T., Nishimura R., Matsunaga S. et al., Syringomyelia and hydrocephalus in a dog, J Am Vet Med Assoc, September (1) 1996, 209(5):934–936. 23. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 499-502.

24. Karmi N., Brown E.A., Hughes S.S. et al., Estimated frequency of the canine hyperuricosuria mutation in different dog breeds, J Vet Intern Med, November-December 2010, 24(6):1337–1342.

Szpic wilczy 1. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010. 2. LaFond E., Breur G., Austin C., Breed susceptibility for developmental orthopedic diseases in dogs, J Am Anim Hosp Assoc, September-October 2002, 38(5):467–477. 3. Weir E., Norrdin R., Barthold S. et al., Primary hyperparathyroidism in a dog: biochemical, bone histomorphometric, and pathologic findings, J Am Vet Med Assoc, December (1) 1986, 189(11):1471–1474. 4. Skelly B., Hyperparathyroidism in the keeshond dog, Vet Rec, 22 May 2004, 154(21):672. 5. Gear R., Neiger R., Skelly B. et al., Primary hyperparathyroidism in 29 dogs: diagnosis, treatment, outcome and associated renal failure, J Small Anim Pract, January 2005, 46(1):10–16. 6. Keeshond Club of America, KCA 2000 Health Survey. 7. Goldstein R., Atwater D., Cazolli D. et al., Inheritance, mode of inheritance, and candidate genes for primary hyperparathyroidism in Keeshonden, J Vet Intern Med, January-February 2007, 21(1):199–203. 8. Patterson D., Pyle R., Van Mierop L. et al., Hereditary defects the conotruncal septum in Keeshond dogs: pathologic and genetic studies, Am J Cardiol, August 1974, 34(2):187–205. 9. Werner P., Raducha M., Prociuk U. et al., The keeshond defect in cardiac conotruncal development is oligogenic, Hum Genet, April 2005, 116(5):368–377. 10. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002, 220(4):466–471. 11. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, 2007. 12. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 13. Hall S., Wallace M., Canine epilepsy: a genetic counselling programme for keeshonds, Vet Rec, April (13) 1996, 138(15):358–360. 14. Wallace M., Keeshonds: a genetic study of epilepsy and EEG readings, J Small Anim Pract, January 1975, 16(1):1–10. 15. Frank L., Hnilica K., Oliver J., Adrenal steroid hormone concentrations in dogs with hair cycle arrest (Alopecia X) before and during treatment with melatonin and mitotane, Vet Dermatol, October 2004, 15(5):278–284. 16. Frank L., Hnilica K., Rohrbach B. et al., Retrospective evaluation of sex hormones and steroid hormone intermediates in dogs with alopecia, Vet Dermatol, April 2003, 14(2):91–97. 17. Kramer J., Klaassen J., Baskin D. et al., Inheritance of diabetes mellitus in Keeshond dogs, Am J Vet Res, March 1988, 49(3):428–431. 18. Kramer J., Nottingham S., Robinette J. et al., Inherited, early onset, insulin-requiring diabetes mellitus of Keeshond dogs, Diabetes, July 1980, 29(7):558–565.

19. Dorn C., Canine breed-specific risks of frequently diagnosed diseases at veterinary teaching hospitals, Monograph, AKC Canine Health Foundation, 2000. 20. Lekcharoensuk C., Lulich J., Osborne C. et al., Patient and environmental factors associated with calcium oxalate urolithiasis in dogs, J Am Vet Med Assoc, August (15) 2000, 217(4):515–519. 21. Murphy C., Marfurt C., McDermott A. et al., Spontaneous chronic corneal epithelial defects (SCCED) in dogs: clinical features, innervation, and effect of topical SP, with or without IGF-1, Invest Ophthalmol Vis Sci, September 2001, 42(10):2252–2261. 22. Ackerman L., The Genetic Connection: A Guide to Health Problems in Purebred Dogs, AAHA Press, 1999, s. 224–225. 23. Klopfer U., Neumann F., Trainin R., Renal cortical hypoplasia in a Keeshond litter, Vet Med Small Anim Clin, September 1975, 70(9):1081–1083. 24. Lassaline M.E., Gelatt K.N., Brooks D.E. et al., Orbitotomy for retrobulbar malignant fibrous histiocytoma in a dog, Vet Ophthalmol, January-February 2005, 8(1):1–6. 25. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 567–571.

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Szwedzki vallhund 1. Evans K., Adams V., Proportion of litters of purebred dogs born by caesarean section, J Small Anim Pract, February 2010, 51(2):113–118. 2. Statystyki rasy OFA: www.offa.org, Dostęp: 1 lipca 2010.

3. American College of Veterinary Ophthalmologists, Ocular Disorders Presumed to be Inherited in Purebred Dogs, ACVO, 2007. 4. Nachreiner R., Refsal K., Graham P. et al., Prevalence of serum thyroid hormone autoantibodies in dogs with clinical signs of hypothyroidism, J Am Vet Med Assoc, February (15) 2002,220(4), s. 466–471. 5. Nachreiner R., Refsal K., Personal communication, Diagnostic Center for Population and Animal Health, Michigan State University, April, 2007. 6. The Complete Dog Book, 20th ed., The American Kennel Club, Howell Book House, NY 2006, s. 706–709.

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Amerykański curl 1. Robinson R., The American Curl cat, J Hered, 1989, 80(6):474–475.

Angora turecka 1. Arikan S., Duru S., Gurkan M. et al., Blood type A and B frequencies in Turkish Van and Angora cats in Turkey, J Vet Med A Physiol Pathol Clin Med, August 2003, 50(6):303– 306. 2. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004.

Egipski mau 1. Little S., Pers. Comm, 2009. 2. Roca A., Nash W., Menninger J.,et al., Insertional polymorphisms of endogenous feline leukemia viruses, J Virol, April 2005, 79(7):3979–3986. 3. Kelly D., Gaskell C., Spongy degeneration of the central nervous system in kittens, Acta Neuropathol (Berl), 1976, 35:151–158.

Highland fold 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 3. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004. 4. Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525.

Japoński bobtail 1. Lipinski M., Froenicke L., Baysac K. et al., The ascent of cat breeds: genetic evaluations of breeds and worldwide random-bred populations, Genomics, January 2008, 91(1):12–21. 2. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 3. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399.

Korat 1. Grahn R., Grahn J., A practical application of the pointing test, Notes, University of California (Davis) Feline Genetics Extravaganza II August 28–29 2004. 2. Menotti-Raymond M., David V., Pflueger S. et al., Patterns of molecular genetic variation among cat breeds, Genomics, January 2008, 91(1):1–11. 3. Muldoon L., Neuwelt E., Pagel M. et al., Characterization of the molecular defect in a feline model for Type II GM2-gangliosidosis (Sandhoff Disease), Am J Pathol, 1994, 144(5):1109–1118. 4. Neuwelt E., Johnson W., Blank N. et al., Characterization of a new model of GM2-gangliosidosis (Sandhoff Disease) in Korat cats, J Clin Invest, 1985, 76:482–490. 5. De Maria R., Divari S., Bo S. et al., β-galactosidase deficiency in a Korat cat: a new form of feline GM1-gangliosidosis, Acta Neuropathol, 1998, 96(3):307–314. 6. Baker H., The molecular basis of feline GM1 and GM2 gangliosidoses, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998, Feline Practice Supplement, 1999, 11. 7. Martin D., Krum B., Varadarajan G. et al., An inversion of 25 base pairs causes feline GM2gangliosidosis variant 0, Exp Neurol, 2004, 187:30–37. 8. Haskins M., Lysosomal storage diseases in cats: An overview, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998, Feline Practice Supplement, 1999, 22. 9. Baker H., Smith B., Martin D. et al., Molecular screening for the feline gangliosidoses in Korats, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998, Feline Practice Supplement, 1999, 22.

Kot abisyński 1. Chew D.J., DiBartola S.P., Boyce J.T. et al., Renal amyloidosis in related Abyssinian cats, J Am Vet Med Assoc, 1982, 181(2):139–142. 2. DiBartola S.P., Familial renal diseases of cats, Proceedings, The North American Veterinary Conference 1999, 326–327. 3. van der Linde-Sipman J.S., Niewold T.A., Tooten P.C.J. et al, Generalized AA-amyloidosis in Siamese and Oriental cats, Vet Immunol Immunopathol, 1997, 56:1–10. 4. Gruys E., van de Stadt M., Blok J.J. et al., Feline Amyloidosis, Proceedings, First International Feline Genetic Disease Conference, [w:] Feline Practice Supplement, 1999, s. 15. 5. Van Rossum M., van Asten F., Rofina J. et al., Analysis of cDNA sequences of feline SAAs, Amyloid, J Protein Folding Disord, 2004, 11:38–43. 6. Anderson R., Maude M., Nilsson S. et al, Plasma lipid abnormalities in 465 the Abyssinian cat with a hereditary rod-cone degeneration, Exp Eye Res, 1991, 53:415–417. 7. Narfström K., Progressive Retinal Atrophy in Abyssinians, Proceedings, First International Feline Genetic Disease Conference Philadelphia June, 1998, [w:] Feline Practice Supplement,1999, s. 21. 8. Narfström K., Hereditary progressive retinal atrophy in the Abyssinian cat, J Hered, 1983, 74:273–276. 9. Wiggert B., van Veen T., Kutty G. et al., An early decrease in interphoto-receptor retinoid-binding protein gene expres-

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sion in Abyssinian cats homozygous for hereditary rod-cone degeneration, Cell Tissue Res, 1994, 278:291–298. Seeliger M., Narfström K., Functional assessment of the regional distribution of disease in a cat model of hereditary retinal degeneration, Invest Ophthalmol Vis Sci, 2000, 41(7):1998–2005. Nilsson S., Mäepea O., Alm A. et al., Ocular blood flow and retinal metabolism in Abyssinian cats with hereditary retinal degeneration, Invest Ophthalmol Vis Sci, 2001, 42(5):1038–1044. Narfström K., Ehinger B., Bruun A., Immunohistochemical studies of cone photoreceptors and cells of the inner retina in feline rod-cone degeneration, Vet Ophthalmol, 2001, 4(2):141–145. May C., Lutjen-Drecoll E., Narfstrom K., Morphological changes in the anterior segment of the Abyssinian cat eye with hereditary rod-cone degeneration, Curr Eye Res, 2005, 30(10):855–862. Narfström K., David V., Jarret O.,et al., Retinal degeneration in the Abyssinian and Somali cat (rdAc): correlation between genotype and phenotype and rdAc allele frequency in two continents, Vet Ophthalmol, 2009, September-October, 12(5):285–291. Narfström K., Hereditary and congenital ocular disease, J Fel Med Surg, 1999, 1:135–141. Menotti-Raymond M., Deckman K., David V. et al., Mutation discovered in a feline model of human congenital retinal blinding disease, Invest Ophthalmol Vis Sci, June 2010, 51(6):2852–2859. Smith S., Tobias A., Jacob K. et al., Arterial thromboembolism in cats: Acute crisis in 127 cases (1992-2001) and long-term management with low-dose aspirin in 24 cases, J Vet Intern Med, 2003, 17:73–83. Bagdi N., Magdus M., Leidinger E. et al., Frequencies of feline blood types in Hungary, Acta Vet Hung, 2001, 49(4):369–375. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. Giger U., Griot-Wenk M., Bucheler J. et al., Geographical variation of the feline blood type frequencies in the United States, Fel Pract, 1991, 19(6):21–27. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. Barrs V., Giger U., Wilson B. et al., Erythrocyte pyruvate kinase deficiency and AB blood types in Australian Abysinnian and Somali cats, Aust Vet J, 2009, 87(1):39–44. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatal isoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, Lake Buena Vista FL 1997, 308–310. Kohn B., Goldschmidt M., Hohenhaus A. et al., Anemia, splenomegaly, and increased osmotic fragility of erythrocytes in Abyssinian and Somali cats, J Am Vet Med Assoc, 2000, 217(10):1483–1491. Giger U., Rajpurohit Y., Skelly B. et al., Erythrocyte pyruvate kinase deficiency in cats, [w:] First International Feline Genetic Disease Conference 1998, Proceedings, Feline Practice Supplement, 1999, s. 8.

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26. Ford S., Giger U., Duesberg C. et al., Inherited erythrocyte pyruvate kinase (PK) deficiency causing hemolytic anemia in an Abyssinian cat, Proceedings, 10th Annual Veterinary Medical Forum, San Diego CA, May 1992, [w:] JACVIM1992, 6:123. 27. Kohn B., Fumi C., Clinical course of pyruvate kinase deficiency in Abyssinian and Somali cats, J Feline Med Surg, April 2008, 10(2):145–153. 28. Lulich J.P., O’Brien T.D., Osborne C.A. et al., Feline Renal Failure: Questions, answers, questions, Compend Contin Educ Pract Vet, 1992, 14(2):127–152. 29. Van Wessum R., Harvey C.E., Hennet P., Feline dental resorptive lesions-prevalence patterns, Vet Clin North Am: Sm Anim Pract, 1992, 22:1405–1416. 30. Lekcharoensuk C., Osborne C.A., Lulich J.P., Epidemiologic study of risk factors for lower urinary tract diseases in cats, J Am Vet Med Assoc, May (1) 2001, 218(9):1429–1435. 31. Fox P.R., Feline cardiomyopathy (Part I), Hypertrophic cardiomyopathy, Proceedings, 19th Annual ACVIM Forum Denver, 2001, 145. 32. Atkins C.E., Feline dilated cardiomyopathy, Proceedings [abstr], Winter 2004 AAFP Meeting [w:] AAFP Newsletter, August 2004, 22(2):29–30. 33. Engvall E., Bushnell N., Patellar luxation in Abyssinian cats, Fel Pract, 1990, 18(4):20–22. 34. Smith G., Lagenbach A., Giger U. et al., Patellar luxation and hip dysplasia in a group of cats, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998 [w:] Feline Practice Supplement, 1999, 23. 35. Little S., Feline hip dysplasia, Notes, Winn Feline Foundation Website, www.winnfelinehealth.org/hip-dysplasia.html Accessed Sep 29, 2004. 36. Smith G., Lagenbach A., Green P. et al., Evaluation of the association between medial patellar luxation and hip dysplasia in cats, J Am Vet Med Assoc, 1999, 215(1):40–45. 37. Lagenbach A., Giger U., Green P. et al, Relationship between degenerative joint disease and hip joint laxity by use of distraction index and Norberg angle measurement in a group of cats, J Am Vet Med Assoc, 1998, 213(10):1439–1443. 38. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, J Feline Med Surg, Februarz 2006, 8(1):1–5. 39. Jones B., Gruffydd-Jones T., Sparkes A. et al.. Preliminary studies on congenital hypothyroidism in a family of Abyssinian cats, Vet Rec, 1992, 131:145–148. 40. Tobias S., Labato M., Identifying and managing feline congenital hypothyroidism, Vet Med, September 2001, 719– 726. 41. Shelton G., Ho M., Kass P., Risk factors for acquired myasthenia gravis in cats: 105 cases (1986–1998), J Am Vet Med Assoc, January (1) 2000, 216(1):55–57. 42. Bagley R., Diseases of the peripheral nervous system, neuromuscular junction and muscle; Evaluation of weakness, Proceedings, AAFP Fall meeting, 1998, 31–33. 43. Baral R., Metcalfe S., Krockenberger M. et al., Disseminated Mycobacterium avium infection in young cats: overrepresen-tation of Abyssinian cats, J Feline Med Surg, February 2006, 8(1):23–44. 44. Langohr I., Tanabe M., Idiopathic complex polysaccharide storage disease in an Abyssinian cat, Vet Pathol, July 2005, 42(4):502–506.

45. Hyman J., Vaegan, Lei B., Narfstrom K., Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration, Am J Vet Res, November 2005, 66(11):1914–1921. 46. Vaegen, Narfstrom K., Optimal discrimination of an Abyssinian cat recessive retinal degeneration: a short electroretinogram protocol is more efficient than a long one, Clin Experiment Ophthalmol, December 2004, 32(6):619–625.

Kot amerykański krótkowłosy 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Meurs K., Inherited heart disease in the cat, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference Oct 2-4, 2003, www.vin.com/tufts/2003. Accessed November 19 2004. 3. Meurs K., Kittleson M., Towbin J. et al., Familial systolic anterior motion of the mitral valve and or hypertrophic cardiomyopathy is apparently inherited as an autosomal dominant trait in a family of American Shorthair cats, Proceedings, 15th Annual ACVIM Veterinary Medical Forum, 1997, 685. 4. Meurs K., Kittleson M., Towbin J. et al., Familial systolic anterior motion of the mitral valve and/or hypertrophic cardiomyopathy is apparently inherited as an autosomal dominant trait in a family of American shorthair cats, J Vet Intern Med, 1997, 11:138 (abstract). 5. Kittleson M., Meurs K., Kittleson J. et al., Heritable characteristics, phenotypic expression, and natural history of hypertrophic cardiomyopathy in Maine Coon cats, [w:] First International Feline Genetic Disease Conference Proceedings, Feline Practice Supplement, 1999. Patrz też: Kittleson M., Meurs K., Kittleson J., Hypertrophic cardiomyopathy in Maine Coon cats. www.winnfelinehealth.org/ reports/cardiomyopathy.html Dostęp 6 sierpnia 2004. 6. Erdman C., Lyons L., Facial Development Study Update, (Aug 2003-Aug 2004), Notes, University of California (Davis) Feline Genetics Extravaganza II August 28–29, 2004. 7. Lyons L., The Lyon’s Den. Feline Genome Project: Cranio-facial Defect, Accessed at http://faculty.vetmed.ucdavis. edu/faculty/lalyons/Sites/ burmese.htm. Accessed November 2004. 8. Lyons L., The Lyons Den Website. Feline Genome Project: Polycystic Kidney Disease, Available at: http:faculty.vetmed.ucdavis.edu/faculty/lalyons/Sites/pkd.htm. Accessed November 6 2004. 9. Washizu T., Washizu M., Zhang C. et al., A suspected case of ornithine transcarbamylase deficiency in a cat, J Vet Med Sci, June 2004, 66(6):701–703. 10. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004.

Kot balijski 1. Baker H., Wood P., Wenger D. et al., Sphingomyelin lipidosis in a cat, Vet Pathol, 1978, 24 (5):386–391. 2. Shell L., A review of feline neuromuscular diseases, [w:] Symposium: Feline Neurologic Diseases, Vet Med, June 1998, 565–574. 3. Di Natale P., Annella T., Daniele A. et al., Animal models for lysosomal storage diseases : A new case of feline mucopolysaccharidosis VI, J Inher Metab Dis, 1992, 15:17–24. 4. Crawley A., Yogalingam G., Muller V. et al., Inherited degenerative joint disease in cats due to mild Mucopolysaccharidosis Type VI, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June, 1998 [w:] Feline Practice Supplement, 1999:30.

Kot bengalski 1. Little S., Bengal Kitten Information Project, Pers Comm, March 2009. 2. Knottenbelt C., Addie D., Day M. et al., Determination of the prevalence of feline blood types in the UK, J of Small Anim Pract, 1999, 40:115–118. 3. Lyons L., Raymond M., O’Brien S., The feline genome project: The role of the genetic map of the cat in fancy cat breeding, Proceedings (abstr), First International Feline Genetic Disease Conference, Feline Practice Supplement, 1999, 20. 4. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, J Feline Med Surg, 2006 Vol 8(1):1–5. 5. Bergvall K., A novel ulcerative nasal dermatitis of Bengal cats, Vet Dermatol, 2004, 15(Suppl. 1):20–40. 6. Granger N., Stalin C., Brown T., Jeffery N., Idiopathic polyradiculoneu-ropathy in a Bengal cat: electrophysiological findings and 1 year follow-up, J Feline Med Surg, December 2008, 10(6):603–607. 7. Pettigrew R., Kent M., Berry W., Shelton A., Muscle and Nerve Biopsies in 138 Cats: Diagnosis and Outcome, http:// www.vin.com/proceedings/Proceedings.plx?CID=WSAVA2002&Category=1319&PID=9729&O=Generic Accessed: August 4 2010. 8. Feline Advisory Board Website, http://www.fabcats.org/breeders/inherited_disorders/bengal.php Accessed: May 2010.

Kot birmański 1. Lipinski M., Young A., Lyons L.. Genetic diversity and population dynamics of domestic cat breeds, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference October 2–4 2003, www.vin.com/tufts/2003 Accessed November 19 2004. 2. Little S., Birman Kitten Information Project, Pers Comm, March 2009. 3. Jensen A., Olesen A., Arnberg J., Distribution of feline blood types detected in the Copenhagen area of Denmark, Acta Vet Scand, 1994, 35:121–124. 4. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20.

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5. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 6. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatal isoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, 1997, 308–310. 7. Knottenbelt C., Addie D., Day M. et al., Determination of the prevalence of feline blood types in the UK, J of Small Anim Pract, 1999, 40:115–118. 8. Gunn-Moore D., Dodkin S., Sparkes A., Letter to the Editor, J Fel Med Surg, 2002, 4:165–166. 9. Hirsch V., Cunningham T., Hereditary anomaly of neutrophil granulation in Birman cats, Am J Vet Res, 1984, 45(10):2170–2174. 10. Bridle K., Littlewood J., Tail tip necrosis in two litters of Birman kittens, J Small Anim Pract, 1998, 39:88–89. 11. Smith S., Tobias A., Jacob K. et al., Arterial thromboembolism in cats: Acute crisis in 127 cases (1992-2001) and long-term management with low-dose aspirin in 24 cases, J Vet Intern Med, 2003, 17:73–83. 12. Narfström K., Hereditary and congenital ocular disease in the cat, J Fel Med Surg, 1999, 1:135–141. 13. Glaze M., Feline corneal diseases: Part II, Proceedings, The 70th Annual AAHA Conference, 2003, 1:367–368. 14. Foley J., Pedersen N., The inheritance of susceptibility to feline infectious peritonitis in purebred catteries, Fel Pract, 1996, 24(1):14–22. 15. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, J Feline Med Surg, Februarz 2006, 8(1):1–5. 16. Hoskins J., Congenital defects in cats, Compend Contin Educ Pract Vet, 1995, 17(3):385–405. 17. Moreau P., Vallat J., Hugon J. et al., Peripheral and central distal axonopathy of suspected inherited origin in Birman cats, ACTA Neuropathol, 1991, 82:143–146. 18. Narfström K., Hereditary eye diseases, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998 [w:] Feline Practice Supplement, 1999, 13. 19. Casal M., Straumann U., Sigg C. et al., Congenital hypotrichosis with thymic aplasia in nine Birman kittens, JAAHA, 1994, 30:600–602. 20. Casal M., Arnold S., Straumann U. et al., Congenital hypotrichosis with thymic aplasia in Birman kittens, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998 [w:] Feline Practice Supplement, 1999, 33–34. 21. Feline Advisory Beaureau Website Accessed May 2010 at: http://www.fabcats.org/breeders/inherited_disorders/birman.php

Kot bombajski 1. Erdman C., Lyons L., Facial Development Study Update (Aug 2003-Aug 2004) [w:] Notes, University of California (Davis) Feline Genetics Extravaganza II Aug 28–29 2004. 2. Jordan E., Black Magic, Cat Fancy, October 2008, 22–25.

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Kot brytyjski krótkowłosy 1. Giger U, Frequency and inheritance of A and B Blood types in feline breeds in the United States, J Hered, 1991, 82:15–20. 2. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 3. Knottenbelt C., Addie D., Day M. et al., Determination of the prevalence of feline blood types in the UK, J Small Anim Pract, 1999, 40:115–118. 4. Little S., Selected inherited diseases of the cat, Proceedings, International Ragdoll Congress October 2004, www.catvet. homestead.com/Inherited_Diseases_2004.pdf Accessed November 23, 2004. 5. Connolly D., Cannata J., Boswood A. et al., Cardiac troponin I in cats with hypertrophic cardiomyopathy, J Fel Med Surg, 2003, 5:209–216. 6. Giger U., Casal M., Niggemeier A, The fading kitten syndrome and neonatal isoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, 1997, 308–310. 7. Narfström K., Hereditary and congenital ocular disease, J Fel Med Surg, 1999, 1:135–141. 8. Brooks M., Factor IX deficiency (Hemophilia B) in two male domestic shorthair cats, JAAHA, 1989, 25:153– 155. 9. Maggio-Price L., Dodds W., Factor IX deficiency (Hemophilia B) in a family of British Shorthair cats, J Am Vet Med Assoc, 1993, 203(12):1702–1704. 10. Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525. 11. Norris J., Bosward K., White J. et al., Clinicopathological findings associated with feline infectious peritonitis in Sydney, Australia: 42 cases (1990-2002), Aust Vet J, November 2005, 83(11):666–673. 12. Tasker S., MacKay A., Sparkes A., A case of feline primary hypoadrenocorticism, J Fel Med Surg, 1999, 1:257–260. 13. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004.

Kot burmski 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Knottenbelt C., Addie D., Day M. et al., Determination of the prevalence of feline blood types in the UK, J Small Anim Pract, 1999, 40:115–118. 3. Little S., Birman Kitten Information Project, Pers Comm, March 2009. 4. Lyons L., The Lyon’s Den. Cranio-facial Deformity, Available at: http://faculty.vetmed.ucdavis.edu/faculty/lalyons/ Sites/burmese.htm Accessed November 15, 2004.

5. Erdman C., Lyons L., Facial Development Study Update, (Aug 2003-Aug 2004), Notes, University of California (Davis) Feline Genetics Extravaganza II August 28–29, 2004. 6. Sponenberg D., Graf-Webster E., Hereditary meningoencephalocele in Burmese cats, J Hered, 1986; 77(1):60. 7. Noden D., Evans H., Inherited homeotic midfacial malformations in Burmese cats, J Craniofac Genet Dev Biol Suppl, 1986, 2:249–266. 8. Hoskins J., Congenital defects in cats, Compend Contin Educ Pract Vet, 1995, 17(3):385–405. 9. Narfström K., Hereditary eye diseases, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June, 1998 [w:] Feline Practice Supplement, 1999:13. 10. Narfström K., Hereditary and congenital ocular disease, J Fel Med Surg, 1999, 1:135–141. 11. Edwards C., Belford C., Hypokalemic polymyopathy in Burmese cats, Aust Vet Practit, 1995, 25(2):58–60. 12. Gaschen F., Jaggy A., Jones B., Congenital diseases of feline muscle and neuromuscular junction, J Fel Med Surg, 2004, 6:355–366. 13. Gruffydd-Jones T., Sparkes A., Caney S. et al., Hypokalemic Episodic weakness in Burmese kittens, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998 [w:] Feline Practice Supplement, 1999:29. 14. Blaxter A., Lievesley P., Gruffydd-Jones T. et al. Periodic muscle weakness in Burmese kittens, Vet Rec, 1986, 118(22):619–620. 15. Taboada J., Ventroflexion of the neck in cats, Proceedings, The 12th ACVIM Veterinary Medical Forum, San Francisco CA, 1994:385–386. 16. Lulich J., O’Brien T., Osborne C. et al., Feline Renal Failure: Questions, answers, questions, Compend Contin Educ Pract Vet, 1992, 14(2):127–152. 17. Panciera D., Thomas C., Eicker S. et al., Epizootiologic patterns of diabetes mellitus in cats: 333 cases (19801986), J Am Vet Med Assoc, 1990, 197(11):1504–1508. 18. Rand J., Current understanding of feline diabetes: Part 1: Pathogenesis, J Fel Med Surg, 1999, 1(3):143–153. 19. Rand J., Bobbermien L., Hendrikz J. et al., Over representation of Burmese cats with diabetes mellitus, Aust Vet J, 1997, 75(6):402–405. 20. Rand J., Fleeman L., Farrow H. et al., Canine and feline diabetes mellitus: Nature or nurture?, J Nutr, 2004, 134:2072S–2080S. 21. Lederer R., Rand J., Jonsson N. et al., Frequency of feline diabetes mellitus and breed predisposition in domestic cats in Australia, Vet J, Februarz 2009, 179(2):254–258. 22. Sturgess C., Waters L., Gruffydd-Jones T. et al., Investigation of the association between whole blood and tissue taurine levels and the development of thoracic deformities in neonatal Burmese kittens, Vet Rec, 1997, 141:566–570. 23. Little S, Breed Specific Reproduction Projects, Notes, University of California (Davis) Feline Genetics Extravaganza I July, 2003. 24. Thumchai R., Lulich J., Osborne C. et al., Epizootiologic evaluation of urolithiasis in cats: 3,498 cases (1982-1992), J Am Vet Med Assoc, 1996, 208(4):547–551. 25. Houston D., Moore A., Favrin M. et al., Feline urethral plugs and bladder uroliths: A review of 5484 submissions 1998-2003, Can Vet J, December 2003, 44(12):974–977.

26. Neilson J., Anxieties, phobias and compulsive disorders, Proceedings, AAFP Fall Conference, 2002, 125–139. 27. Pentlarge V., Corneal sequestration in cats, Compend Contin Educ Pract Vet, 1989, 11(1):24–32. 28. Glaze M., Feline corneal diseases: Part II, Proceedings, The 70th Annual AAHA Conference. 2003, 1:367–368. 29. Fox P. Feline cardiomyopathy (Part I). Hypertrophic cardiomyopathy, Proceedings, The 19th Annual ACVIM Veterinary Medical Forum, Denver CO, 2001:1129. 30. Atkins C., Feline dilated cardiomyopathy, Proceedings [abstr], Winter 2004 AAFP Meeting, AAFP Newsletter, August 2004, 22(2):29–30. 31. Roca A., Nash W., Menninger J. et al., Insertional polymorphisms of endogenous feline leukemia viruses, J Virol, April 2005, 79(7):3979–3986. 32. Hampson E., Smith R., Bernays M., Primary glaucoma in Burmese cats, Aust Vet J, 2002, 80(11):672–680. 33. Jacobi S., Dubielzig R., Feline primary open angle glaucoma, Vet Ophthalmol, May-June 2008, 11(3):162–165. 34. Gunn-Moore D., Crispin S., Unusual ocular condition in Burmese cats, Vet Rec, 1998, 142(12):376. 35. Eason P., Unusual ocular condition in Burmese cats, Vet Rec, 1998, 142(19):524. 36. Hardman C. et al., Proceedings. American College of Veterinary Ophthalmologists, 1999. 37. Kluger E., Hardman C., Govendir M. et al., Triglyceride response following an oral fat tolerance test in Burmese cats, other pedigree cats and domestic crossbred cats, J Feline Med Surg, February 2009, 11(2):82–90. 38. Gunn-Moore D., Watson T., Dodkin S. et al., Transient hyperlipidaemia and anaemia in kittens, Vet Rec, 1997, 140:355–359. 39. Zook B., Paasch L., Endocardial fibroelastosis in Burmese cats, Am J Pathol, 1982, 106(3):435–438. 40. Rozengurt N., Endocardial fibroelastosis in common domestic cats in the UK. J Comp Path, 1994, 110:295–301. 41. Allan G., Radiographic features of feline joint disease, Vet Clin North Am: Sm Anim Pract, 2000, 30(2):281–301. 42. Addie D., Kennedy L., Ryvar R. et al., Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis, J Fel Med Surg, 2004, 6:59–62. 43. Norris J., Bosward K., White J. et al., Clinicopathological findings associated with feline infectious peritonitis in Sydney, Australia: 42 cases (1990-2002), Aust Vet J, November 2005, 83(11):666–673. 44. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, Feline Med Surg, February 2006, 8(1):1–5. 45. Bradbury A., Morrison N., Hwang M. et al., Neurodegenerative lysosomal storage disease in European Burmese cats with hexosaminidase beta-subunit deficiency, Mol Genet Metab, February (20) 2009. 46. Feline Advisory Beaureau Website at: http://www.fabcats. org/breeders/inherited_disorders/burmese.php 47. Engvall E., Bushnell N., Patellar luxation in Abyssinian cats, Fel Pract, 1990, 18(4):20–22. 48. Lyons L., Imes D., Grahn R., Investigation of albinism in domestic cats, Proceedings, The 2nd International Conference Advances in Canine and Feline Genomics, Utrecht Netherlands October 2004. Poster #18. 49. Schmidt-Kuntzel A., Eizirik E., O’Brien S. et al., Tyrosi-

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Literatura zalecana 1. Glaze M., Congenital and hereditary ocular abnormalities in cats, Clin Tech Small Anim Pract, May 2005, 20(2):74–82.

Kot egzotyczny / egzotyczny krótkowłosy 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Barthez P., Rivier P., Begon D., Prevalence of polycystic kidney disease in Persian and Persian-related cats in France, J Fel Med Surg, 2003, 5(6):345–347. 3. Beck C., Lavelle R., Feline polycystic kidney disease in Persian and other cats: a prospective study using ultrasonography, Aust Vet J, 2001, 79(3):181–184. 4. Barrs V., Gunew M., Foster S. et al., Prevalence of autosomal dominant kidney disease in Persian cats and related breeds in Sydney and Brisbane, Aust Vet J, 2001, 79:257–259. 5. Lyons L., The Lyon’s Den. Feline Genome Project: Polycystic Kidney Disease, http://faculty.vetmed.ucdavis.edu/ faculty/lalyons/Sites/pkd.htm, dostęp 6 listopada 2004. 6. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 7. Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525. 8. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004.

Kot hawański 1. Lipinski M., Young A., Lyons L.. Genetic diversity and population dynamics of domestic cat breeds, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference October 2–4 2003, www.vin.com/tufts/2003 Accessed November 19 2004. 2. Lyons L., The Lyon’s Den Website. Breed Diversity and Cat Domestication Project, Available at: http://faculty.vetmed. ucdavis.edu/faculty/lalyons/Sites.... Accessed November 23 2004. 3. Menotti-Raymond M., David V., Pflueger S. et al., Patterns of molecular genetic variation among cat breeds, Genomics, January 2008, 91(1):1–11. 4. Little, S. Pers. Comm. 2009. 5. Brooks M., Feline hereditary coagulopathies, Proceedings (abstr), First International Feline Genetic Disease Conference Philadelphia June 1998, Feline Practice Supplement, 1999, 6, 17, 20.

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Kot himalajski 1. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 2. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 3. Lyons L., The Lyon’s Den. Feline Genome Project: Polycystic Kidney Disease, http://faculty.vetmed.ucdavis.edu/ faculty/lalyons/Sites/pkd.htm, dostęp 6 listopada 2004. 4. Narfström K., Hereditary and congenital ocular disease, J Fel Med Surg, 1999, 1:135–141. 5. Hoskins J., Congenital defects in cats, Compend Contin Educ Pract Vet, 1995, 17(3):385–405. 6. Rubin L., Hereditary cataract in Himalayan cats, Fel Pract, 1986, 16(1):14–15. 7. Pentlarge V., Corneal sequestration in cats, Compend Contin Educ Pract Vet, 1989, 11(1):24–32. 8. Glaze M., Feline corneal diseases: Part II, Proceedings, The 70th Annual AAHA Conference, 2003, 1:367–368. 9. Adamama-Moraitou K., Patsikas M., Koutinas A., Feline lower airway disease: a retrospective study of 22 naturally occurring cases from Greece, J Fel Med Surg, 2004, 6:227–233. 10. La Croix N., van der Woerdt A., Olivero D., Nonhealing corneal ulcers in cats: 29 cases (1991-1999), J Am Vet Med Assoc, 2001, 18(5):733–735. 11. Thumchai R., Lulich J., Osborne C. et al., Epizootiologic evaluation of urolithiasis in cats: 3,498 cases (1982-1992), J Am Vet Med Assoc, 1996, 208(4):547–551. 12. Lekcharoensuk C., Osborne C.A., Lulich J.P., Epidemiologic study of risk factors for lower urinary tract diseases in cats, J Am Vet Med Assoc, May (1) 2001, 218(9):1429– 1435. 13. Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525. 14. Keller G., Reed A., Lattimer J. et al., Hip dysplasia: A feline population study, Veterinary Radiology & Ultrasound, 1999, 40(4):460–464. 15. DeManuelle T., Feline dermatopathies: Newly described disorders, Proceedings, 70th Annual AAHA Conference, 2003, s. 93-95. 16. Levy J., Congenital Portosystemic vascular shunts in cats: 98 cases, (Proceedings) First International Feline Genetic Disease Conference Philadelphia June, 1998, [w:] Feline Practice Supplement, 1999, s. 30. 17. Jones B., Inherited hyperchylomicronaemia in the cat, J of Small Anim Pract, 1993, 34:493–499. 18. Jonsson N., Pullen C., Watson A., Neonatal isoerythrolysis in Himalayan kittens, Austr Vet J, 1990, 67(11):416.

19. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatalisoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, Lake Buena Vista FL, 1997, 308–310. 20. Chaitman J., van der Woerdt A., Bartick T., Multiple eyelid cysts resembling apocrine hidrocystomas in three Persian cats and one Himalayan cat, Vet Pathol, 1999, 36:474–476. 21. French T., Fox L., Randolph J. et al., A bleeding disorder (von Willebrand’s disease) in a Himalayan cat, J Am Vet Med Assoc, 1987, 190(4):437–439. 22. Counts D., Byers P., Holbrook K. et al., Dermatosparaxis in a Himalayan cat: I. Biochemical studies of dermal collagen, J Invest Dermatol, 1980, 74:96–99. 23. Collier L., Leathers C., Counts D., A clinical description of Dermatosparaxis in a Himalayan cat, Fel Pract, 1980, 10(5):25–36. 24. Plotnick A., Brunt J., Reitz B., Cutaneous asthenia in a cat, Fel Pract, 1992, 20(4):9–12. 25. Bradley W., Fibrodysplasia ossificans in a Himalayan cat, Aust Vet Practit, 1992, 22(4):154–158. 26. Bassett J., Hypocalcemia and hyperphosphatemia due to primary hypoparathoidism in a six-month-old kitten, JAAHA, 1998, 34:503–507. 27. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, J Feline Med Surg, Februarz 2006, 8(1):1–5.

Kot kartuski (chartreux) 1. Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525.

Kot colorpoint krótkowłosy 1. Narfström K., Hereditary and congenital ocular disease, J Fel Med Surg, 1999, 1:135–141.

Kot norweski leśny 1. Drögemüller C., Rüfenacht S., Wichert B., Leeb T, Mutation within the FGF5 gene are associated with hair length in cats, Animal Genet, June 2007, 38(3):218–221. 2. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 3. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 4. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatalisoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, Lake Buena Vista FL, 1997, 308–310. 5. Little S., Norwegian Forest Cat Kitten Information Project, Pers. Comm, March, 2009. 6. Gaschen F., Jaggy A., Jones B., Congenital diseases of feline muscle and neuromuscular junction, J Fel Med Surg, 2004, 6:355–366.

7. Fyfe J., Glycogen storage disease Type IV in Norwegian Forest Cats: Molecular detection of carriers [w:] Proceedings, First International Feline Genetic Disease Conference 1998., Feline Practice Supplement, 1999;10. 8. Coates J., Paxton R., Cox N. et al., A case presentation and discussion of Type IV glycogen storage disease in a Norwegian Forest Cat, Progress in Veterinary Neurology, 1996, 7(1):5–11. 9. Fyfe J., Glycogenosis Type IV of Norwegian Forest Cats, Proceedings, 17th Annual Meeting of the American College of Veterinary Internal Medicine, 1999, s. 281. 10. Fyfe J., Giger U., Van Winkle T. et al., Glycogen storage disease type IV: Inherited deficiency of branching enzyme activity in cats, Pediatr Res, December 1992, 32(6):719–725. 11. Fyfe J., Giger U., Van Winkle T. et al., Familial glycogen storage disease (Type IV GSD IV), Proceedings, 8th Annual Meeting of the American College of Veterinary Internal Medicine Veterinary Medical Forum, Washington, DC 1990:1129. 12. Fyfe J., Van Winkle T., Haskins M. et al., Animal model of human disease: Glycogen Storage Disease Type IV, Comp Path Bullet, 1994, 26(3):3–6.

Kot orientalny 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Lekcharoensuk C., Osborne C.A., Lulich J.P., Epidemiologic study of risk factors for lower urinary tract diseases in cats, J Am Vet Med Assoc, May (1) 2001, 218(9):1429– 1435. 3. Lorimer H., Hereditary lymphosarcoma in Oriental shorthair cats, Proceedings, First International Feline Genetic Disease Conference Philadelphia June, 1998, [w:] Feline Practice Supplement,1999, s. 29. 4. Court E., Watson A., Peaston A., Retrospective study of 60 cases of feline lymphosarcoma, Aust Vet J, 1997, 75(6):424–427. 5. Geary L., Lyons L., Lymphosarcoma in Siamese/Oriental Shorthair breeds, Notes, University of California (Davis) Feline Genetics Extravaganza II Aug 28–29, 2004. 6. Lyons L., Geary L., Lymphosarcoma in Siamese/OSH populations, Proceedings of the 2nd International Conference Advances in Canine and Feline Genomics, October 2004, Utrecht Netherlands, Poster #30. 7. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004. 8. Gunn-Moore D., Watson T., Dodkin S. et al., Transient hyperlipidaemia and anaemia in kittens, Vet Rec, 1997, 140:355–359.

Kot perski 1. Giger U., Griot-Wenk M., Bucheler J. et al., Geographical variation of the feline blood type frequencies in the United States, Fel Pract, 1991, 19(6):21–27.

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2. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 3. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 4. Knottenbelt C., Addie D., Day M. et al., Determination of the prevalence of feline blood types in the UK, J of Small Anim Pract, 1999, 40:115–118. 5. Lyons L., Biller D., Erdman C. et al., Feline polycystic kidney disease mutation identified in PKD1, J Am Soc Nephrol, 2004, 15:2548–2555. 6. Drögemüller C., Rüfenacht S., Wichert B., Leeb T, Mutation within the FGF5 gene are associated with hair length in cats, Animal Genet, June 2007, 38(3):218–221. 7. Cooper K., Piveral P., Autosomal dominant polycystic disease in Persian cats, Fel Pract, 2000, 28(2):20–21. 8. DiBartola S., Autosomal dominant polycystic kidney disease, Proceedings, 18th Annual ACVIM Forum, Seattle WA, 2000, s. 438–440. 9. Pedersen K., Pedersen H., Häggström, J. et al., Increased mean arterial pressure and aldosterone-to-renin ratio in Persian cats with polycystic disease, JVIM, 2003, 17(1):21–27. 10. DiBartola S., Familial renal diseases of cats, Proceedings, The North American Veterinary Conference, 1999, s. 326327. 11. Bosje J., van den Ingh T., van der Linde-Simpson J., Polycystic kidney and liver disease in cats, Vet Q, 1998, 20(4):136–140. 12. Malik R, Genetic Diseases of Cats (and Dogs), Proceedings, University of Sydney Post Graduate Foundation in Veterinary Science, Valentine Charlton Refresher Course for Veterinarians, Cats, July 2000, 27-37. 13. Lyons L., Biller D., Autosomal dominant polycystic disease in Persian and Persian-related cats. Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference October 2–4, 2003 VIN: www.vin.com/tufts/2003. Dostęp 23 listopada 2004. 14. Eaton K., Biller D., DiBartola S. et al., Autosomal dominant polycystic kidney disease in Persian and Persian-cross cats, Vet Pathol, 1997, 34:117–126. 15. Biller D., DiBartola S., Eaton K. et al., Inheritance of polycystic kidney disease in Persian cats, J Hered, 1996, 87:1–5. 16. Medinger T., Bruyette D., Feline hypertrophic cardiomyopathy, Compend Contin Educ Pract Vet, 1992, 14(4):479– 490. 17. Atkins C., Feline hypertrophic cardiomyopathy, Winter 2004 AAFP Meeting, Proceedings [w:] AAFP Newsletter, August 2004, 22(2):30–31. 18. Martin L., VandeWoude S., Boon D. et al., Left ventricular hypertrophy in a closed colony of Persian cats, 12th Annual ACVIM Veterinary Medical Forum, San Francisco CA, [w:] JVIM, 1994, 8(2):143. 19. Hoskins J., Congenital defects in cats, Compend Contin Educ Pract Vet, 1995, 17(3):385–405. 20. Levy J., Congenital Portosystemic vascular shunts in cats: 98 cases, (Proceedings) First International Feline Genetic Disease Conference Philadelphia June, 1998, [w:] Feline Practice Supplement, 1999, s. 30.

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21. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatalisoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, Lake Buena Vista FL, 1997, 308–310. 22. Foley J., Pedersen N., The inheritance of susceptibility to feline infectious peritonitis in purebred catteries, Fel Pract, 1996, 24(1):14–22. 23. Addie D., Kennedy L., Ryvar R. et al., Feline leucocyte antigen class II polymorphism and susceptibility to feline infectious peritonitis, J Fel Med Surg, 2004, 6:59–62. 24. Pentlarge V., Corneal sequestration in cats, Compend Contin Educ Pract Vet, 1989, 11(1):24–32. 25. Glaze M., Feline corneal diseases: Part II, Proceedings, The 70th Annual AAHA Conference, 2003, 1:367–368. 26. Featherstone H., Sansom J., Feline corneal sequestra: a review of 64 cases (80 eyes) from 1993 to 2000, Vet Ophthalmol, July-August 2004, 7(4):213–227. 27. 27 La Croix N., van der Woerdt A., Olivero D., Nonhealing corneal ulcers in cats: 29 cases (1991-1999), J Am Vet Med Assoc, 2001, 18(5):733–735. 28. Van Wessum R., Harvey C.E., Hennet P., Feline dental resorptive lesions-prevalence patterns, Vet Clin North Am: Sm Anim Pract, 1992, 22:1405–1416. 29. Houston D., Moore A., Favrin M. et al., Feline urethral plugs and bladder uroliths: A review of 5484 submissions 1998-2003, Can Vet J, December 2003, 44(12):974–977. 30. Thumchai R., Lulich J., Osborne C. et al., Epizootiologic evaluation of urolithiasis in cats: 3,498 cases (1982-1992), J Am Vet Med Assoc, 1996, 208(4):547–551. 31. 31 Lekcharoensuk C., Lulich J., Osborne C. et al., Association between patient-related factors and risk of calcium oxalate and magnesium ammonium phosphate urolithiasis in cats, J Am Vet Med Assoc, August (15) 2000, 217(4):520–525. 32. 32 Lekcharoensuk C., Osborne C.A., Lulich J.P., Epidemiologic study of risk factors for lower urinary tract diseases in cats, J Am Vet Med Assoc, May (1) 2001, 218(9):1429– 1435. 33. Frank A., Norrestam R., Sjodin A., A new urolith in four cats and one dog: composition and crystal structure, J Biol Inorg Chem, April 2002, 7(4–5):437–444. 34. Gunn-Moore D., Thrusfield M., Feline dystocia: prevalence, and association with cranial conformation and breed, Vet Rec, 1995, 136:350–353. 35. Richardson E., Mullen H., Cryptorchidism in cats, Compend Contin Educ Pract Vet, 1993, 15(10):1342–1369. 36. Millis D., Hauptman J., Johnson C., Cryptorchidism and monorchism in cats: 25 cases (1980-1989), J Am Vet Med Assoc, 1992, 200(8):1128–1130. 37. Griffon D., Upper airway obstruction in cats: Pathogenesis and clinical signs, Compend Contin Educ Pract Vet, 2000, 22(9):822–827. 38. Bond R., Curtis C., Ferguson E. et al., An idiopathic facial dermatitis of Persian cats, Vet Dermatol, 2000, 11(1):35–41. 39. Takle G., Hnilica K., Eight emerging feline dermatoses, Vet Med, May 2004, s. 456–467. 40. Schwartz S., Separation anxiety syndrome in cats. 136 cases (1991-2000), J Am Vet Med Assoc, 2002, 220(7):1028–1033. 41. 41 Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October

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Reks kornwalijski 1. Giger U., Blood typing and crossmatching to ensure compatible transfusions, [w:] Bonagura J. (ed.), Kirk’s Current Veterinary Therapy XIII, Philadelphia: WB Saunders Co 2000, 396–399. 2. Giger U., Casal M., Niggemeier A., The fading kitten syndrome and neonatal isoerythrolysis, Proceedings, The 15th Annual ACVIM Medical Forum, Lake Buena Vista FL 1997, 308–310. 3. Giger U., Bucheler J., Patterson D., Frequency and inheritance of A and B blood types in feline breeds of the United States, J Hered, 1991, 82:15–20. 4. Gunn-Moore D., Thrusfield M., Feline dystocia: prevalence, and association with cranial conformation and breed, Vet Rec, 1995, 136:350–353. 5. Little S., Selected inherited diseases of the cat, Proceedings, International Ragdoll Congress October 2004, Pers Comm. 6. Strain G., Hereditary deafness in dogs and cats: Causes, prevalence, and current research, Proceedings, Tuft’s Canine and Feline Breeding and Genetics Conference, October 2–4 2003, http://www.vin.com/tufts/2003. Dostęp 19 listopada 2004. 7. Norris J., Bosward K., White J. et al., Clinicopathological findings associated with feline infectious peritonitis in Sydney, Australia: 42 cases (1990-2002), Aust Vet J, November 2005, 83(11):666–673.

8. Pesteanu-Somogyi L., Radzai C., Pressler B., Prevalence of feline infectious peritonitis in specific cat breeds, J Feline Med Surg, February 2006, 8(1):1–5. 9. Engvall E., Bushnell N., Patellar luxation in Abyssinian cats, Fel Pract, 1990, 18(4):20–22. 10. Robinson R., Genetic aspects of umbilical hernia incidence in cats and dogs, Vet Rec, January (1) 1977, 100(1):9–10. 11. Hoskins J., Congenital defects in cats, Compend Contin Educ Pract Vet, 1995, 17(3):385–405.

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6. DeManuelle T., Feline dermatopathies: Newly described disorders, Proceedings, 70th Annual AAHA Conference, 2003, s. 93–95. 7. Vitale C., Ihrke P., Olivry T. et al., Case Report: Feline urticaria pigmentosa in three related Sphinx cats, Vet Dermatol, 1996, 7:227–233. 8. Jordan, E., Less is More, Cat Fancy, September 2008, s. 26–27. 9. Feline Advisory Beaureau: http://www.fabcats.org/breeders/inherited_disorders/sphynx.php

Syberyjski kot leśny 1. Grahn R., Grahn J., A Practical Application of the Pointing Test, [w:] Notes. University of California (Davis) Feline Genetics Extravaganza II Aug 28-29, 2004. 2. Marek R., Russian Beauty, Cat Fancy, March 2008, s. 47– 49. 3. Feline Advisory Bureau at: http://www.fabcats.org/breeders/inherited_disorders/siberian.php

Turecki van 1. Arikan S., Duru S., Gurkan M. et al., Blood type A and B frequencies in Turkish Van and Angora cats in Turkey, J Vet Med A Physiol Pathol Clin Med, August 2003, 50(6):303– 306. 2. Arikan S., Akkan H., Titres of naturally occurring alloantibodies against feline blood group antigens in Turkish Van cats, J Small Anim Pract, June 2004, 45(6):289–292.

ISBN: 978-83-7579-288-1

RASY PSÓW I KOTÓW

PRZEWODNIK WETERYNARYJNY

prof. dr hab. Roman Lechowski

Jerold S. Bell Kathleen E. Cavanagh Larry P. Tilley Francis W.K. Smith

RASY PSÓW I KOTÓW PRZEWODNIK WETERYNARYJNY Charakterystki ras • Predylekcje do chorób Wskazania diagnostyczne i terapeutyczne 171 ras psów, 42 rasy kotów

Jerold S. Bell, Kathleen E. Cavanagh, Larry P. Tilley, Francis W.K. Smith