233 top medical experts on Alexander Disease across 29 countries and 15 U.S. states, including 68 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Alexander Disease: Rare leukoencephalopathy with infantile-onset accumulation of Rosenthal fibers in the subpial, periventricular, and subependymal zones of the brain. Rosenthal fibers are glial fibrillary acidic protein aggregates found in astrocytes. Juvenile- and adult-onset types show progressive atrophy of the lower brainstem instead. De novo mutations in the gfap gene are associated with the disease with propensity for paternal inheritance.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hereditary Central Nervous System Demyelinating Diseases (1,644), Nervous System Heredodegenerative Disorders (865).
  4. Clinical Trials ClinicalTrials.gov : at least 3 including 3 Recruiting


  

        

                    


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