Search research articles
Contact Us
Filters
Showing results (31-40 of 68) with videos related to
Page
of 7
Sort By:
Israel Journal of Medical Sciences
|
August 1, 1985
High-output cardiac failure as a presenting symptom of plasma cell leukemia
R Tamir, R F Lewin, A Inbal, et al.
Arthritis and Rheumatism
|
April 1, 1989
Hepatic infarction in a patient with the lupus anticoagulant
F Mor, Y Beigel, A Inbal, et al.
Blood
|
April 1, 1990
Molecular studies of von Willebrand disease: reduced von Willebrand factor biosynthesis, storage, and release in endothelial cells derived from patients with type I von Willebrand disease
B M Ewenstein, A Inbal, J S Pober, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Rare bleeding disorders
F Peyvandi, M Cattaneo, A Inbal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 1, 1993
Evaluation of solvent/detergent treated plasma in the management of patients with hereditary and acquired coagulation disorders
A Inbal, O Epstein, D Blickstein, et al.
Thrombosis and Haemostasis
|
December 20, 1993
Effect of type IIB von Willebrand disease mutation Arg(545)Cys on platelet glycoprotein Ib binding--studies with recombinant von Willebrand factor
A Inbal, N Kornbrot, P Harrison, et al.
Thrombosis and Haemostasis
|
May 25, 2001
Pharmacokinetic studies with FVIII/von Willebrand factor concentrate can be a diagnostic tool to distinguish between subgroups of patients with acquired von Willebrand syndrome
J Luboshitz, A Lubetsky, L Schliamser, et al.
Blood
|
April 1, 1996
Analysis of Arg834Gln and Val902Glu type 2A von Willebrand disease mutations: studies with recombinant von Willebrand factor and correlation with patient characteristics
T Englender, A Lattuada, P M Mannucci, et al.
Acta Haematologica
|
January 1, 1985
Hemophagocytosis simulating malignant histiocytosis: a terminal event of the myelodysplastic syndrome
M Prokocimer, A Inbal, M Gelber, et al.
Thrombosis and Haemostasis
|
June 1, 1997
Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab families
A Inbal, V C Yee, N Kornbrot, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 68) with videos related to
Sort By:
Page
of 7
Israel Journal of Medical Sciences
|
August 1, 1985
High-output cardiac failure as a presenting symptom of plasma cell leukemia
R Tamir, R F Lewin, A Inbal, et al.
Arthritis and Rheumatism
|
April 1, 1989
Hepatic infarction in a patient with the lupus anticoagulant
F Mor, Y Beigel, A Inbal, et al.
Blood
|
April 1, 1990
Molecular studies of von Willebrand disease: reduced von Willebrand factor biosynthesis, storage, and release in endothelial cells derived from patients with type I von Willebrand disease
B M Ewenstein, A Inbal, J S Pober, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Rare bleeding disorders
F Peyvandi, M Cattaneo, A Inbal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 1, 1993
Evaluation of solvent/detergent treated plasma in the management of patients with hereditary and acquired coagulation disorders
A Inbal, O Epstein, D Blickstein, et al.
Thrombosis and Haemostasis
|
December 20, 1993
Effect of type IIB von Willebrand disease mutation Arg(545)Cys on platelet glycoprotein Ib binding--studies with recombinant von Willebrand factor
A Inbal, N Kornbrot, P Harrison, et al.
Thrombosis and Haemostasis
|
May 25, 2001
Pharmacokinetic studies with FVIII/von Willebrand factor concentrate can be a diagnostic tool to distinguish between subgroups of patients with acquired von Willebrand syndrome
J Luboshitz, A Lubetsky, L Schliamser, et al.
Blood
|
April 1, 1996
Analysis of Arg834Gln and Val902Glu type 2A von Willebrand disease mutations: studies with recombinant von Willebrand factor and correlation with patient characteristics
T Englender, A Lattuada, P M Mannucci, et al.
Acta Haematologica
|
January 1, 1985
Hemophagocytosis simulating malignant histiocytosis: a terminal event of the myelodysplastic syndrome
M Prokocimer, A Inbal, M Gelber, et al.
Thrombosis and Haemostasis
|
June 1, 1997
Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab families
A Inbal, V C Yee, N Kornbrot, et al.
Page
of 7