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F Rodeghiero

Showing results (201-210 of 266) with videos related to

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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.
Leukemia|July 20, 2007
Aberrant cytoplasmic expression of C-terminal-truncated NPM leukaemic mutant is dictated by tryptophans loss and a new NES motifB Falini, E Albiero, N Bolli, 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.
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Thrombosis Research|February 15, 1993
Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemiaF Rodeghiero, G Castaman, L Gugliotta, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 25, 2008
Laboratory issues in bleeding disordersF Rodeghiero, A Ruiz-Sáez, P H B Bolton-Maggs, 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.
British Journal of Haematology|February 1, 1994
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand diseaseE Fressinaud, A B Federici, G Castaman, et al.
Thrombosis and Haemostasis|May 25, 2001
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factorA C Goodeve, J C Eikenboom, D Ginsburg, et al.
Pageof 27

Showing results (201-210 of 266) with videos related to

Sort By:
Pageof 27
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.
Leukemia|July 20, 2007
Aberrant cytoplasmic expression of C-terminal-truncated NPM leukaemic mutant is dictated by tryptophans loss and a new NES motifB Falini, E Albiero, N Bolli, 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.
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Thrombosis Research|February 15, 1993
Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemiaF Rodeghiero, G Castaman, L Gugliotta, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 25, 2008
Laboratory issues in bleeding disordersF Rodeghiero, A Ruiz-Sáez, P H B Bolton-Maggs, 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.
British Journal of Haematology|February 1, 1994
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand diseaseE Fressinaud, A B Federici, G Castaman, et al.
Thrombosis and Haemostasis|May 25, 2001
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factorA C Goodeve, J C Eikenboom, D Ginsburg, et al.
Pageof 27