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G Castaman

Showing results (141-150 of 198) with videos related to

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Blood|August 1, 1993
Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization methodA Inbal, T Englender, N Kornbrot, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2007
A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3R Schneppenheim, G Castaman, A B Federici, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 2, 2010
von Willebrand's disease diagnosis and laboratory issuesG Castaman, R R Montgomery, S S Meschengieser, et al.
British Journal of Haematology|May 3, 2000
Early haemorrhagic morbidity and mortality during remission induction with or without all-trans retinoic acid in acute promyelocytic leukaemiaE Di Bona, G Avvisati, G Castaman, 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.
Blood|January 1, 1988
von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimersP M Mannucci, R Lombardi, G Castaman, 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.
Blood|October 1, 1996
Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factorJ C Eikenboom, T Matsushita, P H Reitsma, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Pageof 20

Showing results (141-150 of 198) with videos related to

Sort By:
Pageof 20
Blood|August 1, 1993
Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization methodA Inbal, T Englender, N Kornbrot, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2007
A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3R Schneppenheim, G Castaman, A B Federici, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 2, 2010
von Willebrand's disease diagnosis and laboratory issuesG Castaman, R R Montgomery, S S Meschengieser, et al.
British Journal of Haematology|May 3, 2000
Early haemorrhagic morbidity and mortality during remission induction with or without all-trans retinoic acid in acute promyelocytic leukaemiaE Di Bona, G Avvisati, G Castaman, 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.
Blood|January 1, 1988
von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimersP M Mannucci, R Lombardi, G Castaman, 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.
Blood|October 1, 1996
Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factorJ C Eikenboom, T Matsushita, P H Reitsma, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Pageof 20