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Results 1 - 10 of 23 for spinocerebellar disease
  1. Ataxias and Cerebellar or Spinocerebellar Degeneration From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Start Here ... Cerebellar Disorders ... Friedreich Ataxia/Related Issues ... Friedreich Ataxia ... National Institute of Neurological Disorders and Stroke
  2. Friedreich ataxia is a rare disease passed down through families (inherited). It affects the muscles and heart.
  3. Spinocerebellar Ataxias Including Machado-Joseph Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Spinocerebellar ...
  4. ... Joseph disease MJD SCA3 Genetic Testing Registry: Azorean disease Spinocerebellar ataxia type 3 National Organization for Rare Disorders ( ... the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease. Neurol India. 2009 Sep-Oct;57(5):578- ...
  5. ... HT. Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar ...
  6. ... HT. Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar ...
  7. Cerebellar Disorders (National Library of Medicine)  
    When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. ...
  8. Friedreich Ataxia (National Library of Medicine)  
    ... to one side) Heart palpitations, from the heart disease which can happen ... therapy. NIH: National Institute of Neurological Disorders and Stroke
  9. ... LIKE 1; HDL1 HUNTINGTON DISEASE-LIKE 3; HDL3 SPINOCEREBELLAR ATAXIA 17; SCA17 HUNTINGTON DISEASE-LIKE 2; HDL2 PubMed Schneider SA, Walker RH, ...
  10. ... a progressive brain disorder known as Huntington's disease-like 4 (HDL4) or spinocerebellar ataxia type 17 (SCA17). The features of this disorder vary widely among affected individuals. The condition was first described ... including uncontrolled movements, emotional problems, and loss of ...
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