Results 171 to 180 of about 5,479,866 (221)
Some of the next articles are maybe not open access.
Current management of von Willebrand disease and von Willebrand syndrome
Current Opinion in Anaesthesiology, 2014Anesthesiologists frequently care for patients with altered hemostasis and coagulation. Where a clear history of familial and personal bleeding exists, a thoughtful plan can be developed in advance to manage the issue perioperatively. However, in some cases, it may not be known that the patient has a disorder until excessive bleeding is noted during or
Marc E, Stone +3 more
openaire +2 more sources
Acquired von Willebrand syndrome 2004: International Registry
Hamostaseologie, 2004 SummaryThe acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder with laboratory findings similar to those for congenital von Willebrand disease.
A B Federici
exaly +2 more sources
2016
Das von-Willebrand-Syndrom (VWS) ist die haufigste angeborene Blutgerinnungsstorung, die weltweit Manner und Frauen betrifft. Haufig wird das VWS erst nach Blutungskomplikationen diagnostiziert, meistens im Rahmen von Operationen, oder es besteht eine positive Familienanamnese.
Christoph Bidlingmaier +2 more
openaire +2 more sources
Das von-Willebrand-Syndrom (VWS) ist die haufigste angeborene Blutgerinnungsstorung, die weltweit Manner und Frauen betrifft. Haufig wird das VWS erst nach Blutungskomplikationen diagnostiziert, meistens im Rahmen von Operationen, oder es besteht eine positive Familienanamnese.
Christoph Bidlingmaier +2 more
openaire +2 more sources
Management of acquired von Willebrand syndrome
Transfusion and Apheresis Science, 2018Acquired von Willebrand syndrome (AVWS) is a rare acquired bleeding disorder that resembles von Willebrand disease by its clinical symptoms and laboratory findings, but differs by its negative personal and family history of bleeding diathesis. AVWS is mostly seen in the elderly, but it has been described in children, often in those with congenital ...
Janie, Charlebois +2 more
openaire +2 more sources
Treatment of the acquired von Willebrand syndrome
Expert Review of Hematology, 2015Acquired von Willebrand syndrome (aVWS) accounts for 22% of patients with abnormal von Willebrand factor. Most patients with known pathophysiological mechanisms suffer from cardiovascular, myeloproliferative and lymphoproliferative disorders. Less frequent associations are of autoimmune origin, due to hyperfibrinolysis, adsorption to tumor cells ...
Ulrich, Budde +2 more
openaire +2 more sources
1979
Von Willebrand’s disease (VWD) is an inherited bleeding disorder, characterized by spontaneous hemorrhage from mucosal membranes and excessive bleeding following trauma and surgery. Since the original description of the disease [51], it has been recognized that the abnormalities of the hemostatic mechanism are complex [2], a defect of blood coagulation
openaire +2 more sources
Von Willebrand’s disease (VWD) is an inherited bleeding disorder, characterized by spontaneous hemorrhage from mucosal membranes and excessive bleeding following trauma and surgery. Since the original description of the disease [51], it has been recognized that the abnormalities of the hemostatic mechanism are complex [2], a defect of blood coagulation
openaire +2 more sources
Acquired von Willebrand syndrome
Haemophilia, 2008Acquired von Willebrand syndrome (AvWS) is a rare hemorrhagic diathesis with clinical symptoms similar to those associated with the inherited form of von Willebrand disease. This syndrome is characterized by the lack of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age.
M. T. ALVAREZ +4 more
openaire +1 more source
Diagnosis and management of von willebrand's syndrome
Medical Clinics of North America, 1994von Willebrand's disease is the most common of the inherited bleeding disorders. It is caused by quantitative and/or qualitative abnormalities of von Willebrand factor, and it usually presents with bleeding from mucosal surfaces. The diagnosis is confirmed by measuring von Willebrand factor activity and antigen levels, factor VIII activity, and ...
openaire +2 more sources
2005
Erik Adolf von Willebrand, ein finnischer Professor aus Helsinki (Helsingfors) beschrieb 1926 am Beispiel einer Blutersippe von den Aland-Inseln eine neue hereditare hamorrhagische Diathese als »hereditare Pseudohamophilie» (von Willebrand 1926). Im Unterschied zur Hamophilie fand er eine verlangerte Blutungszeit und einen autosomalen Erbgang, der ...
openaire +1 more source
Erik Adolf von Willebrand, ein finnischer Professor aus Helsinki (Helsingfors) beschrieb 1926 am Beispiel einer Blutersippe von den Aland-Inseln eine neue hereditare hamorrhagische Diathese als »hereditare Pseudohamophilie» (von Willebrand 1926). Im Unterschied zur Hamophilie fand er eine verlangerte Blutungszeit und einen autosomalen Erbgang, der ...
openaire +1 more source
Acquired von Willebrand Syndrome
2017The multicenter pilot trial for HeartMate II® (Thoratec, Pleasanton, CA) left ventricular assist systems in 2003 was noticeable, and the rate of bleeding complications was much higher than the rate of thromboembolic events [1]. Initial anticoagulation protocol was decreased; however patients still showed a dysfunction of the primary hemostasis thus ...
Anna L. Meyer, Ivan Netuka
openaire +1 more source