686 top medical experts on Inborn Errors Metabolism across 53 countries and 35 U.S. states, including 572 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Inborn Errors Metabolism: Errors in metabolic processes 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): Metabolic Diseases (2,945), Inborn Genetic Diseases (2,477) and Narrower Categories: Cytochrome-c Oxidase Deficiency (554), Familial Amyloidosis (1,653), Hereditary Hyperbilirubinemia (123), Inborn Amino Acid Transport Disorders (52), Inborn Errors Amino Acid Metabolism (1,295), Inborn Errors Carbohydrate Metabolism (1,325), Inborn Errors Lipid Metabolism (797), Inborn Errors Metal Metabolism (445), Inborn Errors Purine-Pyrimidine Metabolism (580), Inborn Errors Renal Tubular Transport (984), Inborn Errors Steroid Metabolism (385), Inborn Metabolic Brain Diseases (1,358), Lysosomal Storage Diseases (2,636), Peroxisomal Disorders (437), Progeria (2,405).
  4. Clinical Trials ClinicalTrials.gov : at least 84 including 6 Active, 40 Completed, 14 Recruiting
  5. Synonyms: Inborn Errors of Metabolism


  

        

                    


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