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Haemophilia : the Official Journal of the World Federation of Hemophilia|May 15, 2007
Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII geneG Castaman, S H Giacomelli, R Ghiotto, et al.
Journal of Thrombosis and Haemostasis : JTH|September 2, 2009
Molecular and phenotypic determinants of the response to desmopressin in adult patients with mild hemophilia AG Castaman, M E Mancuso, S H Giacomelli, et al.
The New England Journal of Medicine|April 27, 1995
Hydroxyurea for patients with essential thrombocythemia and a high risk of thrombosisS Cortelazzo, G Finazzi, M Ruggeri, et al.
Journal of Thrombosis and Haemostasis : JTH|July 1, 2010
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotypeG Castaman, S H Giacomelli, P Jacobi, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formationG Castaman, S H Giacomelli, P M Jacobi, et al.
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