|
Gait disorders/ataxia
Citations 91-100 of 142 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Paroxysmal dysarthria and ataxia after midbrain infarction
- M. Matsui, H. Tomimoto, K. Sano, K. Hashikawa, H. Fukuyama, and H. Shibasaki
Neurology 2004; 63: 345-347.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration
- Neeraj Kumar, John B. Gross, Jr., and J. Eric Ahlskog
Neurology 2004; 63: 33-39.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Autosomal dominant striatal degeneration (ADSD): Clinical description and mapping to 5q13–5q14
- G. Kuhlenbäumer, P. Lüdemann, A. Schirmacher, E. De Vriendt, G. Hünermund, P. Young, M. Hund-Georgiadis, G. Schuierer, H. Möller, E. B. Ringelstein, C. Van Broeckhoven, V. Timmerman, and F. Stögbauer
Neurology 2004; 62: 2203-2208.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Acute cerebellar ataxia due to Sjögren syndrome
- S. Wong, A. N. Pollock, J. M. Burnham, D. D. Sherry, and D. J. Dlugos
Neurology 2004; 62: 2332-2333.
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Doxifluridine-induced neurotoxicity with normal dihydropyrimidine dehydrogenase activity
- Dong Wook Kim, Han-Joon Kim, Dong-Eog Kim, and Jae-Kyu Roh
Neurology 2004; 62: 2136-2137.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine
- M. Strupp, R. Kalla, M. Dichgans, T. Freilinger, S. Glasauer, and T. Brandt
Neurology 2004; 62: 1623-1625.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Vertical oscillopsia in bilateral superior canal dehiscence syndrome
- A. Deutschländer, M. Strupp, K. Jahn, L. Jäger, F. Quiring, and T. Brandt
Neurology 2004; 62: 784-787.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency
- M. Gironi, C. Lamperti, R. Nemni, M. Moggio, G. Comi, F. R. Guerini, P. Ferrante, N. Canal, A. Naini, N. Bresolin, and S. DiMauro
Neurology 2004; 62: 818-820.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus
- K. Hara, T. Fukushima, T. Suzuki, T. Shimohata, M. Oyake, H. Ishiguro, K. Hirota, A. Miyashita, R. Kuwano, H. Kurisaki, H. Yomono, J. Goto, I. Kanazawa, and S. Tsuji
Neurology 2004; 62: 648-651.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2
- R.A. Maselli, J. Wan, V. Dunne, M. Graves, R.W. Baloh, R.L. Wollmann, and J. Jen
Neurology 2003; 61: 1743-1748.
[Abstract]
[Full text]
[PDF]
|
|
