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Hereditary thrombophilias--recommendations for genetic testing in the clinical praxis

Kvasnicka, J.

Casopis Lekaru Ceskych 149(10): 468-471

2010

ISSN/ISBN: 0008-7335
PMID: 21121136
Document Number: 645513
Venous thromboembolism is a common serious clinical condition, in which genetic factors play an important role, too. The objective of this review is to summarize current knowledge regarding the hereditary thrombophilias and submit their simple classification. Recommended Consensus of the Czech Societies on Thrombosis and Haemostasis, Haematology and Medical Genetics for genetic testing in specific patients' groups at venous thromboembolism high-risk situation is also presented.

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Hamann, U. 2000: Hereditary Breast Cancer: High Risk Genes, Genetic Testing and Clinical Implications Clinical Laboratory 46(9-10): 447-461
Hernández-Bronchud, M. 1996: Hereditary predisposition to breast cancer: assessment of genetic risk and recommendations for the clinical follow-up of high-risk cases Medicina Clinica 107(10): 383-387
Raymond, V.M.; Everett, J.N. 2009: Genetic counselling and genetic testing in hereditary gastrointestinal cancer syndromes Best Practice and Research. Clinical Gastroenterology 23(2): 275-283
Likhtenshteĭn, V.A.; Mugutdinov, T.M.; Solomianskiĭ, A.E. 1977: Clinical and genetic aspects of hereditary acro-osteolysis Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 77(10): 1452-1458
Dadali, E.L.; Illarioshkin, S.N.; Markova, E.D.; Ivanova-Smolenskaia, I.A. 1992: Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 92(4): 10-13
Brunet, J.; Alonso, M.C.; Ojeda, B. 1994: Hereditary breast cancer: genetic bases and clinical features Medicina Clinica 103(16): 623-627
Gnamey, D.; Walbaum, R.; Saint-Aubert, P.; Fontaine, G. 1971: Type C hereditary brachydactyly. Clinical and genetic study of 3 families Annales de Pediatrie 18(6): 438-449
Sharkova, I.V.; Milovidova, T.B.; Dadali, E.L.; Poliakov, A.V. 2012: Clinical-genetic characteristics of hereditary motor-sensory neuropathy type 1 X Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 112(7): 42-47
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
Brzustowicz, L.M.; Allitto, B.A. 1997: Clinical molecular genetic testing Journal of the American Medical Women's Association 52(1): 11-15
La Rocca, E.; Amoroso, S.; Brai, M.; Di Leonardo, S.; Aricò, M. 1986: Hereditary angioedema. Genealogic studies and clinical considerations on 2 genetic forms in a case study of 10 patients Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale Societa Italiana di Dermatologia e Sifilografia 121(3): 203-208
Ohnishi, A. 1995: Clinical, pathologic and molecular genetic studies of patients with hereditary motor and sensory neuropathy (HMSN) Rinsho Shinkeigaku 35(12): 1438-1440
Von Fellenberg, J.; Paternotte, C.; Prud'homme, J.F.; Weissenbach, J.; Hazan, J.; Burgunder, J.M. 1998: Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis Schweizerische Medizinische Wochenschrift 128(26): 1043-1050
Long, S.; Goldblatt, J. 2016: MTHFR genetic testing: Controversy and clinical implications Australian Family Physician 45(4): 237-240
Calzone, K.A. 1997: Genetic predisposition testing: clinical implications for oncology nurses Oncology Nursing Forum 24(4): 712-718
Post, S.G.; Whitehouse, P.J.; Binstock, R.H.; Bird, T.D.; Eckert, S.K.; Farrer, L.A.; Fleck, L.M.; Gaines, A.D.; Juengst, E.T.; Karlinsky, H.; Miles, S.; Murray, T.H.; Quaid, K.A.; Relkin, N.R.; Roses, A.D.; St George-Hyslop, P.H.; Sachs, G.A.; Steinbock, B.; Truschke, E.F.; Zinn, A.B. 1997: The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective JAMA 277(10): 832-836
Svendsen, I.H.; Steensgaard-Hansen, F.; Nordvåg, B.Y. 1999: Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. a clinical, genetic and echocardiographic study of an affected Danish family Ugeskrift for Laeger 161(36): 4995-4999
Prnjavorac, B.; Uzunović-Kamberović, S. 2011: Medical biochemistry in everyday clinical praxis Medicinski Glasnik: Official Publication of the Medical Association of Zenica-Doboj Canton Bosnia and Herzegovina 8(1): 75
Porsová-Dutoit, I. 2008: Place of inhibin B investigation in clinical andrological praxis Vnitrni Lekarstvi 54(11): 1059-1062
Kalousek, I.; Röselová, P.; Otevrelová, P. 2006: NGAL--neutrophil gelatinase associated lipocalin in biochemistry, physiology and clinical praxis Casopis Lekaru Ceskych 145(5): 373-376