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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
January 2, 2001
Two families with combined homozygous/heterozygous factor V Leiden mutation and heterozygous G20210A factor II variant
M Ruggeri, G Castaman, A Tosetto, et al.
American Journal of Hematology
|
April 17, 1998
Low risk of venous thrombosis in two families with combined type I plasminogen deficiency and factor V R506Q mutation
G Castaman, M Ruggeri, A Tosetto, et al.
Acta Haematologica
|
January 1, 1983
Fatal pulmonary embolism and antithrombin III deficiency in adult lymphoblastic leukaemia during L-asparaginase therapy
T Barbui, F Rodeghiero, S Meli, et al.
Thrombosis Research
|
March 1, 1992
The bleeding time in normal subjects is mainly determined by platelet von Willebrand factor and is independent from blood group
F Rodeghiero, G Castaman, M Ruggeri, et al.
Thrombosis and Haemostasis
|
August 1, 1997
The VITA project: phenotypic resistance to activated protein C and FV Leiden mutation in the general population. Vicenza Thrombophilia and Atherosclerosis
A Tosetto, E Missiaglia, E Gatto, et al.
British Journal of Haematology
|
November 1, 1985
Erythrocyte fragmentation in disseminated intravascular coagulation (DIC) in acute leukaemia
F Rodeghiero, G Castaman, L Tonellato, et al.
British Journal of Haematology
|
January 1, 1995
Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand disease
G Castaman, A Lattuada, P M Mannucci, et al.
Thrombosis and Haemostasis
|
January 23, 1992
Subunit composition of plasma von Willebrand factor (vWF) in two uremic patients with acquired vWF abnormalities
G Castaman, F Rodeghiero, A Lattuada, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations
G Castaman, S H Giacomelli, S Duga, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1985
[Therapy with high-dose intravenous gamma globulin in the newborn infant with thrombocytopenia from passive immunization]
G F Ronconi, G Castaman, E Fantuz, et al.
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of 27
Search research articles
Search
Showing results (101-110 of 266) with videos related to
Sort By:
Page
of 27
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
January 2, 2001
Two families with combined homozygous/heterozygous factor V Leiden mutation and heterozygous G20210A factor II variant
M Ruggeri, G Castaman, A Tosetto, et al.
American Journal of Hematology
|
April 17, 1998
Low risk of venous thrombosis in two families with combined type I plasminogen deficiency and factor V R506Q mutation
G Castaman, M Ruggeri, A Tosetto, et al.
Acta Haematologica
|
January 1, 1983
Fatal pulmonary embolism and antithrombin III deficiency in adult lymphoblastic leukaemia during L-asparaginase therapy
T Barbui, F Rodeghiero, S Meli, et al.
Thrombosis Research
|
March 1, 1992
The bleeding time in normal subjects is mainly determined by platelet von Willebrand factor and is independent from blood group
F Rodeghiero, G Castaman, M Ruggeri, et al.
Thrombosis and Haemostasis
|
August 1, 1997
The VITA project: phenotypic resistance to activated protein C and FV Leiden mutation in the general population. Vicenza Thrombophilia and Atherosclerosis
A Tosetto, E Missiaglia, E Gatto, et al.
British Journal of Haematology
|
November 1, 1985
Erythrocyte fragmentation in disseminated intravascular coagulation (DIC) in acute leukaemia
F Rodeghiero, G Castaman, L Tonellato, et al.
British Journal of Haematology
|
January 1, 1995
Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand disease
G Castaman, A Lattuada, P M Mannucci, et al.
Thrombosis and Haemostasis
|
January 23, 1992
Subunit composition of plasma von Willebrand factor (vWF) in two uremic patients with acquired vWF abnormalities
G Castaman, F Rodeghiero, A Lattuada, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations
G Castaman, S H Giacomelli, S Duga, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
July 1, 1985
[Therapy with high-dose intravenous gamma globulin in the newborn infant with thrombocytopenia from passive immunization]
G F Ronconi, G Castaman, E Fantuz, et al.
Page
of 27