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Gait disorders/ataxia
Citations 41-50 of 142 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese
- Y. Onodera, M. Aoki, H. Mizuno, H. Warita, Y. Shiga, and Y. Itoyama
Neurology 2006; 67: 1300-1302.
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- CLINICAL/SCIENTIFIC NOTES
Improvement with corticosteroids and azathioprine in GAD65-associated cerebellar ataxia
- Nikolaus R. McFarland, Ivan S. Login, Samuel Vernon, and Ted M. Burns
Neurology 2006; 67: 1308-1309.
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- BRIEF COMMUNICATIONS
Stiff person syndrome with cerebellar disease and high-titer anti-GAD antibodies
- Goran Rakocevic, Raghavan Raju, Cristina Semino-Mora, and Marinos C. Dalakas
Neurology 2006; 67: 1068-1070.
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- ARTICLES
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10
- M. Wakamiya, T. Matsuura, Y. Liu, G. C. Schuster, R. Gao, W. Xu, P. S. Sarkar, X. Lin, and T. Ashizawa
Neurology 2006; 67: 607-613.
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- BRIEF COMMUNICATIONS
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia
- J.A.P. Hiel, B. G.M. van Engelen, C. M.R. Weemaes, A. Broeks, A. Verrips, H. ter Laak, H. M. Vingerhoets, L. P.W. van den Heuvel, M. Lammens, F. J.M. Gabreëls, J. I. Last, and A. M.R. Taylor
Neurology 2006; 67: 346-349.
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- ARTICLES
Scale for the assessment and rating of ataxia: Development of a new clinical scale
- T. Schmitz-Hübsch, S. Tezenas du Montcel, L. Baliko, J. Berciano, S. Boesch, C. Depondt, P. Giunti, C. Globas, J. Infante, J. -S. Kang, B. Kremer, C. Mariotti, B. Melegh, M. Pandolfo, M. Rakowicz, P. Ribai, R. Rola, L. Schöls, S. Szymanski, B. P. van de Warrenburg, A. Dürr, and T. Klockgether
Neurology 2006; 66: 1717-1720.
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- BRIEF COMMUNICATIONS
Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: Novel mutations in SETX
- T. Asaka, H. Yokoji, J. Ito, K. Yamaguchi, and A. Matsushima
Neurology 2006; 66: 1580-1581.
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- BRIEF COMMUNICATIONS
Evaluation of sleep and daytime somnolence in spinocerebellar ataxia type 6 (SCA6)
- Michael J. Howell, Mark W. Mahowald, and Christopher M. Gomez
Neurology 2006; 66: 1430-1431.
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- ARTICLES
Ataxia with oculomotor apraxia type 2: A clinical, pathologic, and genetic study
- C. Criscuolo, L. Chessa, S. Di Giandomenico, P. Mancini, F. Saccà, G. S. Grieco, M. Piane, F. Barbieri, G. De Michele, S. Banfi, F. Pierelli, N. Rizzuto, F. M. Santorelli, L. Gallosti, A. Filla, and C. Casali
Neurology 2006; 66: 1207-1210.
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- BRIEF COMMUNICATIONS
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon
- Y. Ouyang, Y. Takiyama, K. Sakoe, H. Shimazaki, T. Ogawa, S. Nagano, Y. Yamamoto, and I. Nakano
Neurology 2006; 66: 1103-1104.
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