357 top medical experts on Glycogen Storage Disease across 48 countries and 27 U.S. states, including 181 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
  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 Errors Carbohydrate Metabolism (1,325) and Narrower Categories: Glycogen Storage Disease Type I (1,297), Glycogen Storage Disease Type II (1,026), Glycogen Storage Disease Type III (519), Glycogen Storage Disease Type IIb (602), Glycogen Storage Disease Type IV (243), Glycogen Storage Disease Type V (568), Glycogen Storage Disease Type VI (73), Glycogen Storage Disease Type VII (47).
  4. Clinical Trials ClinicalTrials.gov : at least 93 including 6 Active, 46 Completed, 19 Recruiting
  5. Synonyms: Glycogenosis


  

        

                    


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