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Journal of Thrombosis and Haemostasis : JTH|September 22, 2010
Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficienciesG Castaman, M Platè, S H Giacomelli, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 20, 2010
F8 mRNA studies in haemophilia A patients with different splice site mutationsG Castaman, S H Giacomelli, M E Mancuso, et al.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.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.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.Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2013
The spectrum of factor XI deficiency in ItalyG Castaman, S H Giacomelli, S Caccia, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.Journal of Thrombosis and Haemostasis : JTH|June 22, 2011
Deep intronic variations may cause mild hemophilia AG Castaman, S H Giacomelli, M E Mancuso, et al.Journal of Human Genetics|January 25, 2008
Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia AR Santacroce, M Acquila, D Belvini, et al.Pageof 1