498 top medical experts on von Willebrand Diseases across 39 countries and 33 U.S. states, including 407 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. von Willebrand Diseases: Group of hemorrhagic disorders in which the VON willebrand factor is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor viii, and impaired platelet adhesion.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Blood Platelet Disorders (1,881), Coagulation Protein Disorders (281), Hemorrhagic Disorders (1,310), Inherited Blood Coagulation Disorders (1,267) and Narrower Categories: Type 1 von Willebrand Disease (371), Type 2 von Willebrand Disease (664), Type 3 von Willebrand Disease (313).
  4. Synonyms: Angiohemophilia,  Vascular Hemophilia,  von Willebrand Disease


  

        

                    


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