Muscle disease

Citations 271-280 of 283 total displayed.

Past content (since Jan 2001):

ARTICLES
Sleep-disordered breathing and respiratory failure in acid maltase deficiency

U. Mellies, R. Ragette, C. Schwake, M. Baethmann, T. Voit, and H. Teschler
Neurology 2001; 57: 1290-1295. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Congenital muscular dystrophy with primary partial laminin 2 chain deficiency: Molecular study

Y. He, K. J. Jones, N. Vignier, G. Morgan, M. Chevallay, A. Barois, B. Estournet–Mathiaud, H. Hori, T. Mizuta, F. M.S. Tomé, K. N. North, and P. Guicheney
Neurology 2001; 57: 1319-1322. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK

N. P. Davies, L. H. Eunson, M. Samuel, and M. G. Hanna
Neurology 2001; 57: 1323-1325. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Fibromyalgia is common in patients with transformed migraine

M. F.P. Peres, W. B. Young, A. O. Kaup, E. Zukerman, and S. D. Silberstein
Neurology 2001; 57: 1326-1328. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weakness

Chi-Keung Kong, Chun-Hung Ko, Sui Fan Tong, and Ching-Wan Lam
Neurology 2001; 57: 1121-1124. [Abstract] [Full text] [PDF]  

ARTICLES
Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

J. R. Mendell, C. H. Buzin, J. Feng, J. Yan, C. Serrano, D. S. Sangani, C. Wall, T. W. Prior, and S. S. Sommer
Neurology 2001; 57: 645-650. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Tongue atrophy in facioscapulohumeral muscular dystrophy

G. Yamanaka, K. Goto, T. Matsumura, M. Funakoshi, T. Komori, Y. K. Hayashi, and K. Arahata
Neurology 2001; 57: 733-735. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Coenzyme Q₁₀ reverses pathological phenotype and reduces apoptosis in familial CoQ₁₀ deficiency

S. Di Giovanni, M. Mirabella, A. Spinazzola, P. Crociani, G. Silvestri, A. Broccolini, P. Tonali, S. Di Mauro, and S. Servidei
Neurology 2001; 57: 515-518. [Abstract] [Full text] [PDF]  

ARTICLES
Selective deficiency of -dystroglycan in Fukuyama-type congenital muscular dystrophy

Y.K. Hayashi, M. Ogawa, K. Tagawa, S. Noguchi, T. Ishihara, I. Nonaka, and K. Arahata
Neurology 2001; 57: 115-121. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Myopathy with tubulin-reactive crystalline inclusions

T. H. Vu, A. P. Hays, K. Tanji, D. Younger, G.G. Gundersen, A. Eastwood, C. W. Braun, S. DiMauro, and E. Bonilla
Neurology 2001; 57: 149-152. [Abstract] [Full text] [PDF]  

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