Results 281 to 290 of about 147,268 (335)

The Spectrum of von Willebrand’s Disease

Thrombosis and Haemostasis, 1967
SummaryPatients (from 5 kindreds) with variants of von Willebrand’s disease are described. In one kindred the depression of factor VIII was moderate (20 to 40% of normal) and transfusion of 500 ml of normal plasma led to an increase higher than anticipated and to an almost normal level of factor VIII 17 to 24 hrs later.
E J, Bowie, P, Didisheim, J H, Thompson, C A, Owen   +3 more
openaire   +2 more sources

Pseudotumour in von Willebrand disease

Haemophilia, 2001
Pseudotumour is a rare complication of haemophilia; it has previously been reported in patients with moderate or severe haemophilia and rarely in mild disease. We report a case of a proximal pseudotumour occurring in a 36‐year‐old patient with mild von Willebrand disease (vWD) who made a good recovery with conservative management.
S, Wexler, M, Edgar, A, Thomas, I, Learmonth, G, Scott   +4 more
openaire   +2 more sources

Von Willebrand's disease in pregnancy

The American Journal of Surgery, 1950
Abstract A case is reported of pseudohemophilia in a twenty-one year old white primipara.
J, KOTZ, M S, KAUFMAN, C, HAGEAGE, M, GARFINKLE   +3 more
openaire   +2 more sources

Von Willebrand's Disease

Clinics in Haematology, 1983
T S, Zimmerman, Z M, Ruggeri
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

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, Erik A M, Beckers, Yvonne M C, Henskens   +2 more
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.

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