Hereditary features of haemophilia and their consequences in dog-breeding
Slappendel, R.J.
Tijdschrift voor Diergeneeskunde 107(1): 23-25
1982
ISSN/ISBN: 0040-7453 PMID: 7054921 Document Number: 182837
The severity of haemophilia can vary markedly from 1 family or breed to another, and the consequences regarding the transmission of the disease are discussed with particular reference to a population of Alsatians.
Document emailed within 1 workday
Related Documents
1994: European Self-sufficiency and Haemophilia Prophylaxis: Achievable Goals or Idealistic Concepts? An accord meeting on the future of haemophilia care Blood Coagulation and Fibrinolysis: An International Journal in Haemostasis and Thrombosis 5 Suppl. 4: S1-941994: European Self-sufficiency and Haemophilia Prophylaxis: Achievable Goals or Idealistic Concepts? An accord meeting on the future of haemophilia care Blood Coagulation and Fibrinolysis: An International Journal in Haemostasis and Thrombosis 5 Suppl. 4: S1-94
Brunet, J.; Alonso, M.C.; Ojeda, B. 1994: Hereditary breast cancer: genetic bases and clinical features Medicina Clinica 103(16): 623-627
Lei, W.-T.; Shyur, S.-D.; Huang, L.-H.; Kao, Y.-H.; Lo, C.-Y. 2011: Type i hereditary angioedema in Taiwan -- clinical, biological features and genetic study Asian Pacific Journal of Allergy and Immunology 29(4): 327-331
Brodauf, H. 1970: The constancy of breeding interval in cattle as a breeding measure Deutsche Tierärztliche Wochenschrift 77(16): 398-402 passim
Ben Ahméd, S.; Monastiri, K.; Chouchane, L.; el Ouali, M.; Korbi, S.; Kraiem, C.; Khairi, H.; Bignon, Y.J. 1997: Hereditary predisposition to breast cancer: epidemiologic and clinico-anatomic features in 11 Tunisian families La Tunisie Medicale 75(3): 111-116
Irmejs, A.; Borosenko, V.; Melbarde-Gorkusa, I.; Gardovskis, A.; Bitina, M.; Kurzawski, G.; Suchy, J.; Gorski, B.; Gardovskis, J. 2007: Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in Latvia Anticancer Research 27(1b): 653-658
Milman, N. 1991: Hereditary haemochromatosis in Denmark 1950-1985. Clinical, biochemical and histological features in 179 patients and 13 preclinical cases Danish Medical Bulletin 38(4): 385-393
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Gerlitz, S.; Wessel, G.; Wieberneit, D.; Wegner, W. 1993: The problems of breeding spotted rabbits. 3. Variability of the pigmentation grade, ganglionic intestinal wall supply, relationship to pathogenesis--animal breeding and animal welfare aspects Deutsche Tierärztliche Wochenschrift 100(6): 237-239
Nørby, S.; Rosenberg, T. 1990: Leber's hereditary optic atrophy. a hereditary disease caused by mitochondrial DNA mutation Ugeskrift for Laeger 152(43): 3149-3152
Nüssli, R. 1971: Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption Helvetica Paediatrica Acta 26(5): 637-647
Beauvais, J.M.; Alloysius Joko, P.U.R.W.A.N.T.O. 2007: Part des déplacements réguliers dans la mobilité et conséquences pour le transport collectif guidé - Part of regular displacements in the mobility and consequences for the transportationPart of regular travel in the mobility and consequences for the guided collective transportation Recherche, Transports, Securite (94): 5-10
Vanderstock, L.; Vander Eecken, P.; Vermeersch, H. 1983: Hereditary angioedema. A hereditary disorder in the synthesis of the complement system Acta Oto-Rhino-Laryngologica Belgica 36(3): 418-431
Basdevant, A. 2006: L'obésité : origines et conséquences d'une épidémie - Obesity epidemic : origins and consequences Comptes Rendus. Biologies 329(8): 562-569
Zhao, A.; Brown, G.T.L.; Meissel, K. 2020: Manipulating the consequences of tests: how Shanghai teens react to different consequences Educational Research and Evaluation 26(5-6): 221-251
Eastman, A.; Woodfield, D.G. 1975: Haemophilia a in PNG Papua and new Guinea Medical Journal 18(1): 18-20
Sevilla, T. 2000: The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies Revista de Neurologia 30(1): 71-79
Cole, S. 1976: Splinting in haemophilia PhysioTherapy 62(7): 221
Robertson, M. 1985: The heredity of haemophilia Nature 314(6013): 674-675