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Gait disorders/ataxia
Citations 21-30 of 144 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families
- K. Hara, A. Shiga, H. Nozaki, J. Mitsui, Y. Takahashi, H. Ishiguro, H. Yomono, H. Kurisaki, J. Goto, T. Ikeuchi, S. Tsuji, M. Nishizawa, and O. Onodera
Neurology 2008; 71: 547-551.
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- ARTICLES
SCA Functional Index: A useful compound performance measure for spinocerebellar ataxia
- T. Schmitz-Hübsch, P. Giunti, D. A. Stephenson, C. Globas, L. Baliko, F. Saccà, C. Mariotti, M. Rakowicz, S. Szymanski, J. Infante, B.P.C. van de Warrenburg, D. Timmann, R. Fancellu, R. Rola, C. Depondt, L. Schöls, E. Zdzienicka, J. -S. Kang, S. Döhlinger, B. Kremer, B. Melegh, A. Filla, and T. Klockgether
Neurology 2008; 71: 486-492.
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- ARTICLES
GD1b-specific antibody induces ataxia in Guillain-Barré syndrome
- K. Kaida, K. Kamakura, G. Ogawa, M. Ueda, K. Motoyoshi, M. Arita, and S. Kusunoki
Neurology 2008; 71: 196-201.
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- EDITORIALS
Fine-tuning gait in Parkinson disease
- Michele Tagliati
Neurology 2008; 71: 76-77.
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- ARTICLES
Two-year placebo-controlled trial of botulinum toxin A for leg spasticity in cerebral palsy
- A. P. Moore, R. A. Ade-Hall, C. Tudu Smith, L. Rosenbloom, H.P.J. Walsh, K. Mohamed, and P. R. Williamson
Neurology 2008; 71: 122-128.
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- ARTICLES
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- K. Haugarvoll, R. Rademakers, J. M. Kachergus, K. Nuytemans, O. A. Ross, J. M. Gibson, E-K Tan, C. Gaig, E. Tolosa, S. Goldwurm, M. Guidi, G. Riboldazzi, L. Brown, U. Walter, R. Benecke, D. Berg, T. Gasser, J. Theuns, P. Pals, P. Cras, P. Paul De Deyn, S. Engelborghs, B. Pickut, R. J. Uitti, T. Foroud, W. C. Nichols, J. Hagenah, C. Klein, A. Samii, C. P. Zabetian, V. Bonifati, C. Van Broeckhoven, M. J. Farrer, and Z. K. Wszolek
Neurology 2008; 70: 1456-1460.
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- ARTICLES
Association of gait and balance disorders with age-related white matter changes: The LADIS Study
- H. Baezner, C. Blahak, A. Poggesi, L. Pantoni, D. Inzitari, H. Chabriat, T. Erkinjuntti, F. Fazekas, J. M. Ferro, P. Langhorne, J. O’Brien, P. Scheltens, M. C. Visser, L. O. Wahlund, G. Waldemar, A. Wallin, M. G. Hennerici On behalf of the LADIS Study Group
Neurology 2008; 70: 935-942.
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- VIEWS & REVIEWS
The molar tooth sign: A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families
- M. S. Zaki, A. Abdel-Aleem, G. Abdel-Salam, S. E. Marsh, J. L. Silhavy, A. J. Barkovich, M. E. Ross, S. N. Saleem, W. B. Dobyns, and J. G. Gleeson
Neurology 2008; 70: 556-565.
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- ARTICLES
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
- P. Charles, A. Camuzat, N. Benammar, F. Sellal, A. Destée, A-M Bonnet, S. Lesage, I. Le Ber, G. Stevanin, A. Dürr, A. Brice, and French Parkinson's Disease Genetic Study Group
Neurology 2007; 69: 1970-1975.
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- ARTICLES
Orthostatic myoclonus: A contributor to gait decline in selected elderly
- Graham A. Glass, J. Eric Ahlskog, and Joseph Y. Matsumoto
Neurology 2007; 68: 1826-1830.
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