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Items: 8

1.

Supratentorial and infratentorial damage in spinocerebellar ataxia 2: a diffusion-weighted MRI study.

Salvatore E, Tedeschi E, Mollica C, Vicidomini C, Varrone A, Coda AR, Brunetti A, Salvatore M, De Michele G, Filla A, Pappatà S.

Mov Disord. 2014 May;29(6):780-6. doi: 10.1002/mds.25757. Epub 2013 Dec 27.

PMID:
24375449
2.

Ocular motor characteristics of different subtypes of spinocerebellar ataxia: distinguishing features.

Kim JS, Kim JS, Youn J, Seo DW, Jeong Y, Kang JH, Park JH, Cho JW.

Mov Disord. 2013 Aug;28(9):1271-7. doi: 10.1002/mds.25464. Epub 2013 Apr 22.

PMID:
23609488
3.

Progression markers of Spinocerebellar ataxia 2. A twenty years neurophysiological follow up study.

Velázquez-Perez L, Rodríguez-Labrada R, Canales-Ochoa N, Sanchez-Cruz G, Fernandez-Ruiz J, Montero JM, Aguilera-Rodríguez R, Diaz R, Almaguer-Mederos LE, Truitz AP.

J Neurol Sci. 2010 Mar 15;290(1-2):22-6. doi: 10.1016/j.jns.2009.12.013. Epub 2010 Jan 12.

PMID:
20070987
4.

Identification of alternative splicing of spinocerebellar ataxia type 2 gene.

Affaitati A, de Cristofaro T, Feliciello A, Varrone S.

Gene. 2001 Apr 4;267(1):89-93.

PMID:
11311558
5.

Cognitive deficits in spinocerebellar ataxia 2.

Bürk K, Globas C, Bösch S, Gräber S, Abele M, Brice A, Dichgans J, Daum I, Klockgether T.

Brain. 1999 Apr;122 ( Pt 4):769-77.

PMID:
10219787
6.
7.

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families.

Dürr A, Smadja D, Cancel G, Lezin A, Stevanin G, Mikol J, Bellance R, Buisson GG, Chneiweiss H, Dellanave J, et al.

Brain. 1995 Dec;118 ( Pt 6):1573-81.

PMID:
8595486
8.

Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).

Dürr A, Brice A, Lepage-Lezin A, Cancel G, Smadja D, Vernant JC, Agid Y.

Clin Neurosci. 1995;3(1):12-6. Review.

PMID:
7614088

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