Consulte los últimos artículos sobre la enfermedad de von Willebrand
Última actualización: Jueves, 07 de noviembre de 2024The occurrence of unexplained severe bleeding, especially in childhood, can be related to coagulation pathway disorders, associated or not with maltreatment. In such cases of severe bleeding or intracerebral...
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People with a severe von Willebrand disease (VWD) bleeding phenotype experience frequent, prolonged and excessive mucocutaneous bleeding, such as epistaxis, gingival or gastrointestinal (GI) bleeding,...
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Type 3 von Willebrand disease (VWD), an inherited blood disorder, is caused by a total deficiency of von Willebrand factor (VWF), associated to very low levels of factor VIII (FVIII) [1]. Bleeding manifestations...
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Von Willebrand factor (VWF) has an important function in primary haemostasis by mediating the adhesion and aggregation of platelets at the site of injury. Von Willebrand disease (VWD) is caused by a deficiency of VWF and is characterized by a heterogeneous bleeding phenotype. The disease is categorized into three types: VWD with reduced VWF levels (type 1), dysfunctional VWF (type 2) or absence of VWF (type 3).
The objective severity classification...
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2 Retrospective chart review of GI bleeding in people with von Willebrand disease
Haemophilia 2024; 30(4): 970-803 Patient‐reported data on the severity of Von Willebrand disease
Haemophilia 2024; AOP: 10.1111/hae.15103Refine su búsqueda de información científica
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