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American Journal of Hematology
|
December 1, 1993
Multimeric pattern of plasma and platelet von Willebrand factor is normal in uremic patients
G Castaman, F Rodeghiero, A Lattuada, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
October 1, 1993
Ex vivo experimental thrombosis in variants of von Willebrand disease
E Fressinaud, A B Federici, G Castaman, et al.
British Journal of Haematology
|
January 29, 2000
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutation
G Castaman, J C Eikenboom, A Lattuada, et al.
Acta Haematologica
|
January 1, 1987
Recurrent life-threatening epistaxis in a child with Bernard-Soulier syndrome controlled by bilateral ligation of external carotids and ethmoidal arteries
F Rodeghiero, G Castaman, G Pesavento, et al.
Blood
|
May 16, 1998
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system
N Takahashi, H Tsukamoto, H Umeyama, et al.
American Journal of Hematology
|
August 1, 1995
Platelet von Willebrand factor abnormalities in myeloproliferative syndromes
G Castaman, A Lattuada, M Ruggeri, et al.
Blood
|
October 9, 1998
Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance: comparison of three different therapeutic approaches
A B Federici, F Stabile, G Castaman, et al.
Thrombosis and Haemostasis
|
May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
J C Eikenboom, G Castaman, H L Vos, et al.
Haematologica
|
January 4, 1998
Pilot study on the safety and efficacy of desmopressin for the treatment or prevention of bleeding in patients with hematologic malignancies
G Castaman, E D Bona, C Schiavotto, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 20, 2006
Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: a prospective study comparing patients with single (R1205H) and double (R1205H-M740I) defect
G Castaman, A B Federici, M Bernardi, et al.
Page
of 20
Search research articles
Search
Showing results (111-120 of 198) with videos related to
Sort By:
Page
of 20
American Journal of Hematology
|
December 1, 1993
Multimeric pattern of plasma and platelet von Willebrand factor is normal in uremic patients
G Castaman, F Rodeghiero, A Lattuada, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
October 1, 1993
Ex vivo experimental thrombosis in variants of von Willebrand disease
E Fressinaud, A B Federici, G Castaman, et al.
British Journal of Haematology
|
January 29, 2000
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutation
G Castaman, J C Eikenboom, A Lattuada, et al.
Acta Haematologica
|
January 1, 1987
Recurrent life-threatening epistaxis in a child with Bernard-Soulier syndrome controlled by bilateral ligation of external carotids and ethmoidal arteries
F Rodeghiero, G Castaman, G Pesavento, et al.
Blood
|
May 16, 1998
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system
N Takahashi, H Tsukamoto, H Umeyama, et al.
American Journal of Hematology
|
August 1, 1995
Platelet von Willebrand factor abnormalities in myeloproliferative syndromes
G Castaman, A Lattuada, M Ruggeri, et al.
Blood
|
October 9, 1998
Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance: comparison of three different therapeutic approaches
A B Federici, F Stabile, G Castaman, et al.
Thrombosis and Haemostasis
|
May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
J C Eikenboom, G Castaman, H L Vos, et al.
Haematologica
|
January 4, 1998
Pilot study on the safety and efficacy of desmopressin for the treatment or prevention of bleeding in patients with hematologic malignancies
G Castaman, E D Bona, C Schiavotto, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 20, 2006
Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: a prospective study comparing patients with single (R1205H) and double (R1205H-M740I) defect
G Castaman, A B Federici, M Bernardi, et al.
Page
of 20