218 top medical experts on Oculopharyngeal Muscular Dystrophy across 28 countries and 11 U.S. states, including 45 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Oculopharyngeal Muscular Dystrophy: An autosomal dominant hereditary disease that presents in late in life and is characterized by dysphagia and progressive ptosis of the eyelids. Mutations in the gene for poly(A)-binding protein II have been associated with oculopharyngeal muscular dystrophy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Muscular Dystrophies (1,543).
  4. Clinical Trials ClinicalTrials.gov : at least 12 including 5 Completed, 1 Recruiting


  

        

                    


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