|
Gait disorders/ataxia
Citations 81-90 of 142 total displayed.
|
Past content
(since Jan 2001):
|
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- ARTICLES
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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians
- G. Stevanin, A. Durr, C. Dussert, C. Penet, and A. Brice
Neurology 2004; 63: 936.
[Full text]
[PDF]
- NEUROIMAGES
Asymmetric freezing of gait in hemiparkinsonism-hemiatrophy
- Phil Hyu Lee, Uk Sik Joo, Suk Woo Yong, and Kyoon Huh
Neurology 2004; 63: E7.
[Full text]
[PDF]
|
|
