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Muscle disease
Citations 51-60 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease
- G. Kawahara, M. Okada, N. Morone, C. A. Ibarra, I. Nonaka, S. Noguchi, Y. K. Hayashi, and I. Nishino
Neurology 2007; 69: 1043-1049.
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- ARTICLES
Phase II/III randomized trial of TCH346 in patients with ALS
- R. Miller, W. Bradley, M. Cudkowicz, J. Hubble, V. Meininger, H. Mitsumoto, D. Moore, H. Pohlmann, D. Sauer, V. Silani, M. Strong, M. Swash, E. Vernotica, and The TCH346 Study Group
Neurology 2007; 69: 776-784.
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- CLINICAL/SCIENTIFIC NOTES
TOXOCARIASIS OF THE CNS SIMULATING ACUTE DISSEMINATED ENCEPHALOMYELITIS
- C. Marx, J. Lin, M. R. Masruha, M. G. Rodrigues, A. J. da Rocha, L.C.P. Vilanova, and A. A. Gabbai
Neurology 2007; 69: 806-807.
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- ARTICLES
GNE protein expression and subcellular distribution are unaltered in HIBM
- S. Krause, A. Aleo, S. Hinderlich, L. Merlini, I. Tournev, M. C. Walter, Z. Argov, S. Mitrani-Rosenbaum, and H. Lochmüller
Neurology 2007; 69: 655-659.
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- ARTICLES
Limb-girdle muscular dystrophy in the Netherlands: Gene defect identified in half the families
- A. J. van der Kooi, W. S. Frankhuizen, P. G. Barth, C. J. Howeler, G. W. Padberg, F. Spaans, A. R. Wintzen, J.H.J. Wokke, G. -J.B. van Ommen, M. de Visser, E. Bakker, and H. B. Ginjaar
Neurology 2007; 68: 2125-2128.
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- CLINICAL/SCIENTIFIC NOTES
NEW SKELETAL MYOPATHY AND CARDIOMYOPATHY ASSOCIATED WITH A MISSENSE MUTATION IN MYH7
- N. Darin, H. Tajsharghi, I. Östman-Smith, T. Gilljam, and A. Oldfors
Neurology 2007; 68: 2041-2042.
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- ARTICLES
Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
- R. Ben Yaou, A. Toutain, T. Arimura, L. Demay, C. Massart, C. Peccate, A. Muchir, S. Llense, N. Deburgrave, F. Leturcq, K. E. Litim, N. Rahmoun-Chiali, P. Richard, D. Babuty, D. Récan-Budiartha, and G. Bonne
Neurology 2007; 68: 1883-1894.
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- ARTICLES
Orthopedic outcomes of long-term daily corticosteroid treatment in Duchenne muscular dystrophy
- W. M. King, R. Ruttencutter, H. N. Nagaraja, V. Matkovic, J. Landoll, C. Hoyle, J. R. Mendell, and J. T. Kissel
Neurology 2007; 68: 1607-1613.
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- ARTICLES
Symptomatic dysferlin gene mutation carriers: Characterization of two cases
- I. Illa, N. De Luna, R. Domínguez-Perles, R. Rojas-García, C. Paradas, J. Palmer, C. Márquez, P. Gallano, and E. Gallardo
Neurology 2007; 68: 1284-1289.
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- CLINICAL/SCIENTIFIC NOTES
Autosomal dominant primary lateral sclerosis
- Nicolas Dupré, Paul N. Valdmanis, Jean-Pierre Bouchard, and Guy A. Rouleau
Neurology 2007; 68: 1156-1157.
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