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Blood|August 25, 2001
Functional mapping of anti-factor IX inhibitors developed in patients with severe hemophilia BO D Christophe, P J Lenting, G Cherel, et al.Archives of Disease in Childhood|July 11, 1998
A prospective 10 year follow up study of patients with neurofibromatosis type 1M H Cnossen, A de Goede-Bolder, K M van den Broek, et al.Journal of Thrombosis and Haemostasis : JTH|December 21, 2010
Impact of von Willebrand disease on health-related quality of life in a pediatric populationE M de Wee, K Fijnvandraat, A de Goede-Bolder, et al.Human Mutation|January 1, 1997
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?M H Cnossen, M N van der Est, M H Breuning, et al.Thrombosis and Haemostasis|September 28, 2011
Gynaecological and obstetric bleeding in moderate and severe von Willebrand diseaseE M De Wee, H M Knol, E P Mauser-Bunschoten, et al.Journal of Thrombosis and Haemostasis : JTH|March 30, 2010
Health-related quality of life among adult patients with moderate and severe von Willebrand diseaseE M de Wee, E P Mauser-Bunschoten, J G Van Der Bom, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 5, 2003
In vivo recovery and safety of human factor VIII product AAFACT in patients with haemophilia AP J M Vossebeld, M H Tissing, H M Van Den Berg, et al.Pageof 2