نتایج جستجو برای: von willebrand disease

تعداد نتایج: 1579959  

Journal: :The Southeast Asian journal of tropical medicine and public health 2005
Ponlapat Rojnuckarin Benjaporn Akkawat Tanin Intragumtornchai

Type I von Willebrand disease (vWD) is very common in caucasians. Its genetic basis is possibly heterogenous, lying both within and out of the vWF gene locus. We sought to investigate vWF levels in the Thai population, to compare with those of western countries. The vWF antigen and activity were measured using ELISA and Collagen Binding Assay (CBA), respectively, in 311 healthy Thai volunteers....

Journal: :Blood 1982
H R Gralnick S B Williams B C Shafer L Corash

A form of von Willebrand's disease has been described with enhanced ristocetin-induced platelet aggregation and anodal migration of the factor VIII/von Willebrand factor protein (type IIb). We studied two families with this form of von Willebrand's disease and macrothrombocytopenia. We have found that these platelets bind more of the normal and intermediate-sized multimers of the factor VIII/vo...

Journal: :British journal of haematology 2010
Giancarlo Castaman Alberto Tosetto Anne Goodeve Augusto B Federici Stefan Lethagen Ulrich Budde Javier Batlle Dominique Meyer Claudine Mazurier Jenny Goudemand Jeroen Eikenboom Reinhard Schneppenheim Jorgen Ingerslev David Habart Frank Hill Ian Peake Francesco Rodeghiero

The relationships between the Platelet Function Analyzer (PFA)-100 and von Willebrand factor (VWF) levels and bleeding score (BS) were evaluated within a multicentre project on Molecular and Clinical Markers for the Diagnosis and Management of type 1 von Willebrand disease (MCMDM-1VWD). PFA-100 closure time, either with epinephrine (EPI) or adenosine diphosphate (ADP)-cartridges, was measured i...

Journal: :Acta haematologica 2012
Augusto B Federici Paula James

Von Willebrand disease type 3 (VWD3) is the most severe form of this bleeding disorder due to the almost complete deficiency of von Willebrand factor (VWF). VWD3 is inherited as an autosomal recessive trait. While heterozygous carriers exhibit mild or no bleeding symptoms, most patients with VWD3, which is characterized by undetectable levels of VWF antigen (VWF:Ag) and reduced concentrations (...

Journal: :Blood 2016
Barbara A Konkle

for repeat testing. The authors’ conclusion that it should be considered for screening patients requires further consideration and study but conceivably, this assay should improve the future of VWD diagnosis. Conflict-of-interest disclosure: P.D.J. has received research funding from Bayer, CSL Behring, and Octapharma; and honoraria for educational talks from Baxalta, CSL Behring, and Octapharma. n

2010
Christian Rosser

To what extent were Woodrow Wilson’s ideas about public administration informed by German organic political theory? Drawing on the writings of Wilson, Lorenz von Stein, and Johann K. Bluntschli on public administration, and comparing American and German primary sources, the author off ers insights into Wilson’s general concept of public administration, as well as his understanding of the politi...

Journal: :Thrombosis and haemostasis 2014
M Franchini P M Mannucci

Von Willebrand disease (VWD), the most common genetic bleeding disorder, is characterised by a quantitative or qualitative defect of von Willebrand factor (VWF). Patients with VWD suffer from mucocutaneous bleeding, of severity usually proportional to the degree of VWF defect. In particular, gastrointestinal bleeding associated with angiodysplasia is often a severe symptom of difficult manageme...

Journal: :Blood 1989
P M Mannucci A Lattuada G Castaman R Lombardi M L Colibretti N Ciavarella F Rodeghiero

To characterize the heterogeneity of severe (type III) von Willebrand disease (vWD), plasma and platelet von Willebrand factor antigen (vWF:Ag) and ristocetin cofactor activity (Ricof) were measured in 28 obligatory heterozygotes (ie, parents or children of probands from 15 different kindreds with severe vWD). On the average, heterozygotes had low levels of vWF in both platelets and plasma. The...

Journal: :Blood advances 2017
Margaret V Ragni

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