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Gait disorders/ataxia
Citations 81-90 of 144 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures
- R. Straussberg, L. Basel-Vanagaite, S. Kivity, R. Dabby, S. Cirak, P. Nurnberg, T. Voit, M. Mahajnah, D. Inbar, G. M. Saifi, J. R. Lupski, V. Delague, A. Megarbane, A. Richter, E. Leshinsky, and S. F. Berkovic
Neurology 2005; 64: 142-144.
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- BRIEF COMMUNICATIONS
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
- A. Brussino, C. Gellera, A. Saluto, C. Mariotti, C. Arduino, B. Castellotti, M. Camerlingo, V. de Angelis, L. Orsi, P. Tosca, N. Migone, F. Taroni, and A. Brusco
Neurology 2005; 64: 145-147.
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- ARTICLES
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
- T. E. Dudding, K. Friend, P. W. Schofield, S. Lee, I. A. Wilkinson, and R. I. Richards
Neurology 2004; 63: 2288-2292.
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- BRIEF COMMUNICATIONS
Ataxia with oculomotor apraxia type 1 in Southern Italy: Late onset and variable phenotype
- C. Criscuolo, P. Mancini, F. Saccà, G. De Michele, A. Monticelli, L. Santoro, V. Scarano, S. Banfi, and A. Filla
Neurology 2004; 63: 2173-2175.
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- BRIEF COMMUNICATIONS
Clinical phenotype of Brazilian families with spinocerebellar ataxia 10
- H. A.G. Teive, B. B. Roa, S. Raskin, P. Fang, W. O. Arruda, Y. Correa Neto, R. Gao, L. C. Werneck, and T. Ashizawa
Neurology 2004; 63: 1509-1512.
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- ARTICLES
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement
- G. Van Goethem, P. Luoma, M. Rantamäki, A. Al Memar, S. Kaakkola, P. Hackman, R. Krahe, A. Löfgren, J. J. Martin, P. De Jonghe, A. Suomalainen, B. Udd, and C. Van Broeckhoven
Neurology 2004; 63: 1251-1257.
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Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3
- U. Rüb, K. Bürk, L. Schöls, E. R. Brunt, R. A.I. de Vos, G. Orozco Diaz, K. Gierga, E. Ghebremedhin, C. Schultz, D. Del Turco, M. Mittelbronn, G. Auburger, T. Deller, and H. Braak
Neurology 2004; 63: 1258-1263.
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- ARTICLES
Diabetes mellitus and progression of rigidity and gait disturbance in older persons
- Z. Arvanitakis, R. S. Wilson, J. A. Schneider, J. L. Bienias, D. A. Evans, and D. A. Bennett
Neurology 2004; 63: 996-1001.
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- CLINICAL/SCIENTIFIC NOTES
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation
- E. E. Kors, A. Melberg, K. R.J. Vanmolkot, E. Kumlien, J. Haan, R. Raininko, R. Flink, H. B. Ginjaar, R. R. Frants, M. D. Ferrari, and A. M.J.M. van den Maagdenberg
Neurology 2004; 63: 1136-1137.
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- BRIEF COMMUNICATIONS
Aprataxin gene mutations in Tunisian families
- R. Amouri, M. -C. Moreira, M. Zouari, G. El Euch, C. Barhoumi, M. Kefi, S. Belal, M. Koenig, and F. Hentati
Neurology 2004; 63: 928-929.
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