Diagnosis and management of inherited von Willebrand disease in the next decade: a clinical perspective

Diagnosis and management of inherited vo

Diagnosis and management of inherited von Willebrand disease in the next decade: panel discussion

✍ Peter Kouides; Augusto B. Federici; Andra H. James; Erik Berntorp; Thomas Abshir 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 93 KB

Detailed von Willebrand factor multimer

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)

✍ U. BUDDE; R. SCHNEPPENHEIM; J. EIKENBOOM; A. GOODEVE; K. WILL; E. DREWKE; G. CAS 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 401 KB

Detailed von Willebrand factor multimer

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD): a rebuttal

✍ E. J. FAVALORO 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB

Detailed von Willebrand factor multimer

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD): reply to a rebuttal

✍ U. BUDDE; A. B. FEDERICI; A. GOODEVE; J. EIKENBOOM; R. SCHNEPPENHEIM 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 75 KB

Clinical and laboratory diagnosis of von

Clinical and laboratory diagnosis of von Willebrand disease: A synopsis of the 2008 NHLBI/NIH guidelines

✍ William L. Nichols; Margaret E. Rick; Thomas L. Ortel; Robert R. Montgomery; J. 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 310 KB

## Abstract Von Willebrand factor (VWF) mediates blood platelet adhesion and accumulation at sites of blood vessel injury, and also carries coagulation factor VIII (FVIII) that is important for generating procoagulant activity. Von Willebrand disease (VWD), the most common inherited bleeding disord

Clinical use of Haemate-P in inherited v

Clinical use of Haemate-P in inherited von Willebrand’s disease: a patient with type 3 VWD and recurrent menometrorrhagia

✍ R. DOLATKHAH; I. A. KERMANI; Z. SANAAT; S. SEIFI; J. E. ZIAEI; A. NIKANFAR; A. E 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB