338 top medical experts on Leber Hereditary Optic Atrophy across 53 countries and 15 U.S. states, including 175 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Leber Hereditary Optic Atrophy: A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Mitochondrial Diseases (3,186), Hereditary Optic Atrophies (523).
  4. Clinical Trials ClinicalTrials.gov : at least 27 including 3 Active, 13 Completed, 4 Recruiting


  

        

                    


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