227 top medical experts on Cystinuria across 28 countries and 15 U.S. states, including 81 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Cystinuria: An inherited disorder due to defective reabsorption of cystine and other basic amino acids by the proximal renal tubules. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; lysine; arginine; and ornithine. Mutations involve the amino acid transport protein gene SLC3A1.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Renal Aminoacidurias (82).
  4. Clinical Trials ClinicalTrials.gov : at least 21 including 1 Active, 6 Completed, 8 Recruiting


  

        

                    


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