561 top medical experts on Spinocerebellar Ataxias across 48 countries and 32 U.S. states, including 437 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinocerebellar Ataxias: A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes polyneuropathy; dysarthria; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Cerebellar Ataxia (1,479), Spinocerebellar Degenerations (2,263) and Narrower Categories: Ataxia Telangiectasia (2,645), Machado-Joseph Disease (1,661).
  4. Clinical Trials ClinicalTrials.gov : at least 76 including 8 Active, 37 Completed, 16 Recruiting
  5. Synonyms: Spinocerebellar Ataxia Type 1,  Spinocerebellar Ataxia Type 2,  Spinocerebellar Ataxia Type 4,  Spinocerebellar Ataxia Type 5,  Spinocerebellar Ataxia Type 6,  Spinocerebellar Ataxia Type 7,  Spinocerebellar Atrophies


  

        

                    


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