245 top medical experts on Epidermolysis Bullosa Simplex across 37 countries and 20 U.S. states, including 82 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Epidermolysis Bullosa Simplex: A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode keratin-5 and keratin-14 have been associated with several subtypes of epidermolysis bullosa simplex.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Epidermolysis Bullosa (2,065).
  4. Clinical Trials ClinicalTrials.gov : at least 17 including 1 Active, 5 Completed, 6 Recruiting
  5. Synonyms: Epidermolysis Bullosa Herpetiformis Dowling-Meara,  Epidermolysis Bullosa Simplex Kobner,  Weber-Cockayne Syndrome


  

        

                    


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