Results 311 to 320 of about 151,232 (337)

Platelet-type von Willebrand’s Disease

Clinics in Laboratory Medicine, 1984
Platelet-type von Willebrand's disease is a recently described disorder of primary hemostasis, possessing attributes both of von Willebrand's disease and of a qualitative platelet abnormality. This article discusses the clinical features, laboratory aspects, pathophysiology, and treatment of platelet-type von Willebrand's disease.
openaire   +3 more sources

Erik von Willebrand— von Willebrand's Disease

Mayo Clinic Proceedings, 1996
M A, Shampo, R A, Kyle
openaire   +2 more sources

Von Willebrand’s disease

The Indian Journal of Pediatrics, 1993
I M, Nilsson, S, Lethagen
openaire   +2 more sources

von Willebrand's disease

The American Journal of Medicine, 1963
M, BLOMBACK, J E, JORPES, I M, NILSSON
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von Willebrand's factor and von Willebrand's disease.

Current opinion in hematology, 1997
von Willebrand's factor is required for platelet adhesion to subendothelium, and for normal factor VIII survival in the circulation. These functions require the assembly of von Willebrand's factor into multimers that exhibit properly regulated binding to platelet glycoprotein lb. Recent studies suggest that the propeptide of von Willebrand's factor may
T, Matsushita, Z, Dong, J E, Sadler
openaire   +1 more source

[Von Willebrand factor and Von Willebrand disease].

Nederlands tijdschrift voor geneeskunde, 2014
Von Willebrand factor (VWF) is a multimeric adhesive protein that binds platelets to exposed subendothelium and carries factor VIII in the circulation. VWD is classified into three major subtypes, distinguished by a quantitative deficiency of VWF (type 1: partial deficiency; type 3: complete deficiency) or qualitative defects of VWF (type 2A, 2B, 2M ...
Paul W M, Verhezen, Erik A M, Beckers, Yvonne M C, Henskens   +2 more
openaire   +1 more source

How I treat type 2B von Willebrand disease.

Blood, 2018
R. Kruse-Jarres, J. Johnsen
semanticscholar   +1 more source

von Willebrand factor and von Willebrand disease.

Blood, 1987
Progress has occurred in the past several years in the understanding of the structure and function of von Willebrand factor (vWF). This multimeric glycoprotein exhibits a dual role, that of mediating platelet adhesion and aggregation onto thrombogenic surfaces, and that of functioning as carrier in plasma for the factor VIII procoagulant protein.
Z M, Ruggeri, T S, Zimmerman
openaire   +1 more source

VON WILLEBRAND'S DISEASE

The Lancet, 1974
E M, BARROW, J B, GRAHAM
openaire   +2 more sources

Von Willebrand's Disease

Medical Clinics of North America, 1972
E J, Bowie, C A, Owen
openaire   +2 more sources