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Results 1 - 10 of 19 for Spinocerebellar ataxia 2
  1. Spinocerebellar ataxia type 2 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov SPINOCEREBELLAR ATAXIA 2; SCA2 PubMed Almaguer-Mederos LE, Falcon NS, Almira ... PubMed Lastres-Becker I, Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  2. ATXN2 gene 
    ... ClinVar Lastres-Becker I, Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  3. Ataxia with oculomotor apraxia 
    ... SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, non-Friedreich type 1 Genetic Testing Registry: ... apraxia type 1 Ataxia-oculomotor apraxia type 4 Spinocerebellar ataxia with axonal neuropathy type 2 ... for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  4. Spinocerebellar ataxia type 1 
    ... BP, Bauer P, Schols L. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Mov Disord. 2008 Nov 15; ... P. Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1. Cerebellum. 2008;7(2):106-14. doi: 10.1007/s12311-008-0009- ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  5. ITPR1 gene 
    ... indicate that ITPR1 gene mutations that cause the spinocerebellar ataxias affect different regions of the protein than do ... and symptoms among Gillespie syndrome and the various spinocerebellar ataxias. IP3R IP3R1 Tests of ITPR1 PubMed SPINOCEREBELLAR ATAXIA ...
    https://medlineplus.gov/genetics/gene/itpr1 - Genetics
  6. Spinocerebellar ataxia type 36 
    ... doi: 10.1002/mds.25092. Epub 2012 Jul 2. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  7. Huntington's disease-like syndrome 
    ... LIKE 1; HDL1 HUNTINGTON DISEASE-LIKE 3; HDL3 SPINOCEREBELLAR ATAXIA 17; SCA17 HUNTINGTON DISEASE-LIKE 2; HDL2 PubMed Schneider SA, Walker RH, Bhatia KP. ...
    https://medlineplus.gov/.../huntingtons-disease-like-syndrome - Genetics
  8. Spinocerebellar ataxia type 6 
    ... Central Kordasiewicz HB, Gomez CM. Molecular pathogenesis of spinocerebellar ataxia type 6. Neurotherapeutics. 2007 Apr;4(2):285-94. doi: 10.1016/j.nurt.2007. ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  9. ABCB7 gene 
    ... a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia. J Hum Genet. 1998;43(2):115-22. doi: 10.1007/s100380050051. Citation on ...
    https://medlineplus.gov/genetics/gene/abcb7 - Genetics
  10. TBP gene 
    ... X. Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17. Eur J Hum Genet. 2008 Feb;16(2):215-22. doi: 10.1038/sj.ejhg.5201954. Epub 2007 Nov 28. Citation on PubMed Rasmussen A, De Biase I, ... instability in spinocerebellar ataxia type 17. Ann Neurol. 2007 Jun;61(6): ...
    https://medlineplus.gov/genetics/gene/tbp - Genetics
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