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All Neuromuscular Disease
Citations 71-80 of 158 total displayed.
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Past content
(since Jan 2000):
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- CLINICAL/SCIENTIFIC NOTES
Improvement of Satoyoshi syndrome with tacrolimus and corticosteroids
- K. Endo, T. Yamamoto, K. Nakamura, A. Hoshi, T. Yamanoi, A. Watanabe, and M. Homma
Neurology 2003; 60: 2014-2015.
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- EDITORIALS
Strokes, thromboembolic events, and IVIg: Rare incidents blemish an excellent safety record
- Marinos C. Dalakas and Wayne M. Clark
Neurology 2003; 60: 1736-1737.
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- BRIEF COMMUNICATIONS
The clinical features of 16 cases of stroke associated with administration of IVIg
- James B. Caress, Michael S. Cartwright, Peter D. Donofrio, and James E. Peacock, Jr.
Neurology 2003; 60: 1822-1824.
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- BRIEF COMMUNICATIONS
Palmaris brevis spasm: An occupational syndrome
- R. Liguori, V. Donadio, V. Di Stasi, C. Cianchi, and P. Montagna
Neurology 2003; 60: 1705-1707.
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- BRIEF COMMUNICATIONS
Religiousness is related to quality of life in patients with ALS
- Susan M. Walsh, Barbara A. Bremer, Stephanie H. Felgoise, and Zachary Simmons
Neurology 2003; 60: 1527-1529.
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- ARTICLES
Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS
- P.G. Ince, J. Evans, M. Knopp, G. Forster, H.H.M. Hamdalla, S.B. Wharton, and P.J. Shaw
Neurology 2003; 60: 1252-1258.
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- ARTICLES
Primary lateral sclerosis: A heterogeneous disorder composed of different subtypes?
- P. Zhai, F. Pagan, J. Statland, J. A. Butman, and M. K. Floeter
Neurology 2003; 60: 1258-1265.
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- BRIEF COMMUNICATIONS
High rate of constitutional chromosomal rearrangements in apparently sporadic ALS
- T. Meyer, B. Alber, K. Roemer, T. Martin, V.M. Kalscheuer, E. Göttert, K.D. Zang, A.C. Ludolph, H.-H. Ropers, and J. Prudlo
Neurology 2003; 60: 1348-1350.
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- BRIEF COMMUNICATIONS
Carnitine palmitoyltransferase II deficiency: Molecular and biochemical analysis of 32 patients
- T. Wieser, M. Deschauer, K. Olek, T. Hermann, and S. Zierz
Neurology 2003; 60: 1351-1353.
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- BRIEF COMMUNICATIONS
X-linked myotubular myopathy in a female infant caused by a new MTM1 gene mutation
- Ulrike Schara, Wolfram Kress, Jens Tücke, and Wilhelm Mortier
Neurology 2003; 60: 1363-1365.
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