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Gait disorders/ataxia
Citations 1-10 of 119 total displayed.
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Most recent content
(15 Apr 2008):
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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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Past content
(since Jan 2001):
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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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- CLINICAL/SCIENTIFIC NOTES
ATYPICAL CLINICAL COURSE OF FXTAS: RAPIDLY PROGRESSIVE DEMENTIA AS THE MAJOR SYMPTOM
- M.R.R. Gonçalves, L. P. Capelli, R. Nitrini, E. R. Barbosa, C. S. Porto, L. T. Lucato, and A. M. Vianna-Morgante
Neurology 2007; 68: 1864-1866.
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- ARTICLES
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication
- J. Fuchs, C. Nilsson, J. Kachergus, M. Munz, E.-M Larsson, B. Schüle, J. W. Langston, F. A. Middleton, O. A. Ross, M. Hulihan, T. Gasser, and M. J. Farrer
Neurology 2007; 68: 916-922.
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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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