نتایج جستجو برای: von willebrand factor

تعداد نتایج: 931957  

Journal: :American Journal of Clinical Pathology 2011

2013
Thierry Hernández-Gilsoul Yemil Atisha-Fregoso Angel G Vargas-Ruíz Eduardo Rivero-Sigarroa Guillermo Dominguez-Cherit Silvio A Ñamendys-Silva

INTRODUCTION Acquired von Willebrand disease is initiated by autoantibodies and hyperviscosity syndrome caused by a massive polyclonal hypergammaglobulinemia. Acquired von Willebrand disease associated with autoimmune disease in addition to pulmonary hypertension during emergency room presentation is a rare condition. To the best of our knowledge, this is the second case reported in the literat...

Journal: :Journal of Thrombosis and Haemostasis 2012

2014
Steven de Maat Simon F. De Meyer Michel W. J. Smeets Arjan D. Barendrecht Mark Roest Gerard Pasterkamp Karen Vanhoorelbeke Philip G. de Groot

Add f C d Abstract: Background—Von Willebrand factor (VWF) multimer size is controlled through continuous

Journal: :Blood 1991
R Castillo J Monteagudo G Escolar A Ordinas M Magallón J Martín Villar

Platelet von Willebrand factor (vWF) has been suggested to play an important role in the hemostatic process. Clinical and experimental data indicate that bleeding time (BT) and platelet-vessel wall interaction cannot be normalized unless the defect of platelet vWF is also corrected. We have examined the effect of normal platelet concentrate transfusion 1 hour after cryoprecipitate infusion in f...

Journal: :Pediatric emergency medicine practice 2015
Kevin R Schwartz Max Rubinstein

Hemophilia and von Willebrand disease are the most common inherited bleeding disorders encountered in the emergency department. Evidence suggests that the management of bleeding disorders in the emergency department is currently suboptimal, and literature to guide evaluation and management in this setting is limited, though some guidelines do exist. The emergency clinician must have a high inde...

Journal: :Thrombosis and haemostasis 2007
Zaverio M Ruggeri

Looking back at the last thirty years of studies on von Willebrand factor is a lesson on the importance of combining clinical observations with basic research. Most of what we know today originates from the perceptive evaluation of patients with congenital disorders of haemostasis such as haemophilia and von Willebrand disease. Understanding the causes of these diseases was akin to the current ...

Journal: :Blood 1993
M R Ledford I Rabinowitz J E Sadler J W Kent F Civantos

A variant of von Willebrand disease (vWD) was identified in six members of a kindred spanning four generations. The proband was a 46-year-old woman with a lifelong history of bleeding, a prolonged bleeding time (> 15 minutes), markedly elevated von Willebrand factor (vWF) antigen (vWF:Ag = 2.09 U/mL), slightly reduced ristocetin cofactor activity, and a plasma vWF multimer pattern similar to th...

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