207 top medical experts on Inborn Errors Pyruvate Metabolism across 23 countries and 19 U.S. states, including 53 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Inborn Errors Pyruvate Metabolism: Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders.
  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: Leigh Disease (2,203), Pyruvate Carboxylase Deficiency Disease (67), Pyruvate Dehydrogenase Complex Deficiency Disease (338).
  4. Clinical Trials ClinicalTrials.gov : at least 13 including 2 Active, 3 Completed, 6 Recruiting


  

        

                    


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