Results 261 to 270 of about 79,137 (303)
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Von Willebrand's Disease

Clinics in Haematology, 1983
T S, Zimmerman, Z M, Ruggeri
openaire   +3 more sources

Women with von Willebrand disease

Hämostaseologie, 2004
SummaryThe clinical presentation of VWD shows sex-related differences of symptoms. In women the most typical symptoms are menorrhagia, bleeding during and after delivery or abortion and bleeding in connection with caesarean section or gynaecological surgery. Menorrhagia is one of the most common symptoms presented to gynaecologists.
openaire   +2 more sources

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   +2 more
openaire   +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 factor and von Willebrand disease.

[Rinsho ketsueki] The Japanese journal of clinical hematology, 2017
von Willebrand factor (VWF) has two major roles in hemostasis, as a form of molecular glue which functions in platelet plug formation and as a protective transporter for coagulation factor VIII (FVIII). VWF shows a multimeric chain structure composed of 270 kDa subunits containing binding domains for FVIII, platelet and collagens. Biosynthesis, storage,
Taei, Matsui, Jiharu, Hamako
openaire   +1 more source

Von Willebrand Disease

Clinics in Haematology, 1985
L, Holmberg, I M, Nilsson
openaire   +2 more sources

Von Willebrand's Disease

Journal of Pediatric and Adolescent Gynecology, 2007
openaire   +2 more sources

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