Results 121 to 125 of about 567,487 (125)

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

Haemophilia, 2006
F. Herrmann, G. Auerswald, A. Ruiz‐Saez, M. Navarrete, H. Pollmann, S. Lopaciuk, A. Bátorová, Karin Wulff   +7 more
semanticscholar   +1 more source

Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency

European Journal of Clinical Investigation, 2015
Serdar Epçaçan, M. Menegatti, S. Akbayram, A. Cairo, F. Peyvandi, A. F. Oner   +5 more
semanticscholar   +1 more source

Acquired Factor X Deficiency in a Patient with Amyloidosis

Thrombosis and Haemostasis, 1962
K. Korsan‐Bengtsen, P. Hjort, J. Ygge
semanticscholar   +1 more source

Replacement therapy for congenital Factor X deficiency

Transfusion, 1985
R. Knight, C. Barr, B. Alving
semanticscholar   +1 more source

Molecular analysis of the genotype-phenotype relationship in factor X deficiency

Human Genetics, 2000
D. Millar, L. Elliston, P. Deex, M. Krawczak, A. Wacey, J. Reynaud, H. Nieuwenhuis, P. Bolton-Maggs, P. Mannucci, J. Reverter, P. Cachia, K. Pasi, D. Layton, D. Cooper   +13 more
semanticscholar   +1 more source