Spinocerebellar ataxia type 17 (SCA17): Oculomotor phenotype and clinical characterization of 15 Italian patients-Reference-Cited by-同舟云学术

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Spinocerebellar ataxia type 17 (SCA17): Oculomotor phenotype and clinical characterization of 15 Italian patients

Published:2007-10-15 Issue:11 Volume:254 Page:1538-1546
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Mariotti C.,Alpini D.,Fancellu R.,Soliveri P.,Grisoli M.,Ravaglia S.,Lovati C.,Fetoni V.,Giaccone G.,Castucci A.,Taroni F.,Gellera C.,Donato S.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-007-0579-7.pdf

Reference45 articles.

1. Abele M, Bürk K, Andres F, Topka H, Laccone F, Bosch S, Brice A, Cancel G, Dichgans J, Klockgether T (1997) Autosomal dominant cerebellar ataxia type 1.Nerve conduction and evoked potential studies in families with SCA1, SCA2, and SCA3. Brain 120:2141–2148

2. Bauer P, Laccone F, Rolfs A,Wullner U, Bosch S, Peters H, Liebscher S, Scheible M, Epplen JT,Weber BH,Holinski- Feder E,Weirich-Schwaiger H,Morris- Rosendahl DJ,Andrich J, Riess O (2004) Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington’s disease-like phenotype. J Med Genet 41:230–232

3. Brazzelli M, Capitani E, Della Sala S, Spinnler H, Zuffi M (1994) A neuropsychological instrument adding to the description of patients with suspected cortical dementia: the Milan overall dementia assessment. J Neurol Neurosurg Psychiatry 57:1510–1517

4. Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N,Di Donato S, Taroni F (2004) Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families. Arch Neurol 61:727–733

5. Burk K, Fetter M, Abele M, Laccone F, Brice A, Dichgans J, Klockgether T (1999) Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3. J Neurol 246:789–797

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