304 top medical experts on Primary Hyperoxaluria across 43 countries and 21 U.S. states, including 145 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Primary Hyperoxaluria: A genetic disorder characterized by excretion of large amounts of oxalates in urine; nephrolithiasis; nephrocalcinosis; early onset of renal failure; and often a generalized deposit of calcium oxalate. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hyperoxaluria (1,150), Inborn Errors Carbohydrate Metabolism (1,325).
  4. Clinical Trials ClinicalTrials.gov : at least 36 including 4 Active, 17 Completed, 7 Recruiting
  5. Synonyms: Primary Oxaluria


  

        

                    


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