281 top medical experts on Inborn Errors Carbohydrate Metabolism across 43 countries and 26 U.S. states, including 115 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Inborn Errors Carbohydrate Metabolism: Dysfunctions of carbohydrate metabolism resulting from inborn genetic mutations that are inherited or acquired in utero.
  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 Metabolism (1,547) and Narrower Categories: Congenital Disorders of Glycosylation (2,322), Fucosidosis (131), Galactosemias (1,096), Glucosephosphate Dehydrogenase Deficiency (867), Glycogen Storage Disease (1,538), Inborn Errors Fructose Metabolism (31), Inborn Errors Pyruvate Metabolism (334), Lactose Intolerance (1,301), Mannosidase Deficiency Diseases (22), Mucolipidoses (1,443), Mucopolysaccharidoses (1,530), Multiple Carboxylase Deficiency (21), Primary Hyperoxaluria (1,333).
  4. Clinical Trials ClinicalTrials.gov : at least 13 including 5 Completed, 1 Recruiting


  

        

                    


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