200 top medical experts on Nesidioblastosis across 17 countries and 5 U.S. states, including 24 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Nesidioblastosis: An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the pancreas and congenital hyperinsulinism. It is due to focal hyperplasia of pancreatic islet cells budding off from the ductal structures and forming new islets of Langerhans. Mutations in the islet cells involve the potassium channel gene kcnj11 or the ATP-binding cassette transporter gene abcc8, both on chromosome 11.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Congenital Hyperinsulinism (1,585).
  4. Clinical Trials ClinicalTrials.gov : at least 41 including 1 Active, 20 Completed, 9 Recruiting
  5. Synonyms: with Pancreatic Nesidioblastosis Familial Hyperinsulinism


  

        

                    


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