277 top medical experts on Inherited Blood Coagulation Disorders across 47 countries and 27 U.S. states, including 117 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Inherited Blood Coagulation Disorders: Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), Blood Coagulation Disorders (2,664) and Narrower Categories: Activated Protein C Resistance (600), Afibrinogenemia (1,444), Antithrombin III Deficiency (751), Bernard-Soulier Syndrome (445), Factor VII Deficiency (830), Factor V Deficiency (719), Factor XIII Deficiency (833), Factor XII Deficiency (226), Factor XI Deficiency (637), Factor X Deficiency (482), Gray Platelet Syndrome (307), Hemophilia A (3,685), Hemophilia B (1,216), Hermanski-Pudlak Syndrome (953), Hypoprothrombinemias (261), Protein C Deficiency (872), Thrombasthenia (972), Wiskott-Aldrich Syndrome (1,437), von Willebrand Diseases (1,013).
  4. Clinical Trials ClinicalTrials.gov : at least 5 including 1 Active, 3 Recruiting
  5. Synonyms: Inherited Coagulation Disorders,  Hereditary Coagulation Disorders,  Inherited Coagulation Disorders


  

        

                    


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