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Gait disorders/ataxia
Citations 31-40 of 142 total displayed.
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Past content
(since Jan 2001):
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- NEUROIMAGES
Acute reversible cerebellar lesions associated with metronidazole therapy
- Joshua L. Bonkowsky, Cole Sondrup, and Susan L. Benedict
Neurology 2007; 68: 180.
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- CLINICAL/SCIENTIFIC NOTES
Homer 3 autoimmunity in subacute idiopathic cerebellar ataxia
- L. Zuliani, L. Sabater, A. Saiz, J. J. Baiges, B. Giometto, and F. Graus
Neurology 2007; 68: 239-240.
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- BRIEF COMMUNICATIONS
A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada
- P. N. Valdmanis, D. Brunet, J. St-Onge, L. Weston, G. A. Rouleau, and N. Dupré
Neurology 2006; 67: 2239-2242.
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- ARTICLES
Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2)
- I. Tuin, U. Voss, J. -S. Kang, K. Kessler, U. Rüb, D. Nolte, H. Lochmüller, S. Tinschert, D. Claus, K. Krakow, B. Pflug, H. Steinmetz, and G. Auburger
Neurology 2006; 67: 1966-1972.
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- CLINICAL/SCIENTIFIC NOTES
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5
- D. N. Lorenzo, S. M. Forrest, Y. Ikeda, K. A. Dick, L.P.W. Ranum, and M. A. Knight
Neurology 2006; 67: 2084-2085.
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- BRIEF COMMUNICATIONS
Phenotypic homogeneity of the Huntington disease–like presentation in a SCA17 family
- S. A. Schneider, B.P.C. van de Warrenburg, T. D. Hughes, M. Davis, M. Sweeney, N. Wood, N. P. Quinn, and K. P. Bhatia
Neurology 2006; 67: 1701-1703.
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- BRIEF COMMUNICATIONS
Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia
- J. C. Jen, H. Lee, Y. H. Cha, S. F. Nelson, and R. W. Baloh
Neurology 2006; 67: 1704-1706.
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- ARTICLES
Molecular and imaging correlates of the fragile X–associated tremor/ataxia syndrome
- S. Cohen, K. Masyn, J. Adams, D. Hessl, S. Rivera, F. Tassone, J. Brunberg, C. DeCarli, L. Zhang, J. Cogswell, D. Loesch, M. Leehey, J. Grigsby, P. J. Hagerman, and R. Hagerman
Neurology 2006; 67: 1426-1431.
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- BRIEF COMMUNICATIONS
Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats
- H. Ito, H. Kawakami, R. Wate, S. Matsumoto, T. Imai, A. Hirano, and H. Kusaka
Neurology 2006; 67: 1479-1481.
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- ARTICLES
The contactin 4 gene locus at 3p26 is a candidate gene of SCA16
- S. Miura, H. Shibata, H. Furuya, Y. Ohyagi, M. Osoegawa, Y. Miyoshi, H. Matsunaga, A. Shibata, N. Matsumoto, A. Iwaki, T. Taniwaki, H. Kikuchi, J. Kira, and Y. Fukumaki
Neurology 2006; 67: 1236-1241.
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