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Muscle disease
Citations 61-70 of 283 total displayed.
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Past content
(since Jan 2001):
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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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- CLINICAL/SCIENTIFIC NOTES
Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy
- Homa Tajsharghi, Anders Oldfors, Dominic P. Macleod, and Michael Swash
Neurology 2007; 68: 962.
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- ARTICLES
Distal arthrogryposis and muscle weakness associated with a ß-tropomyosin mutation
- H. Tajsharghi, E. Kimber, D. Holmgren, M. Tulinius, and A. Oldfors
Neurology 2007; 68: 772-775.
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- EDITORIALS
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
- Steven A. Greenberg and George W. Padberg
Neurology 2007; 68: 544-545.
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- ARTICLES
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
- R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Neurology 2007; 68: 569-577.
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- ARTICLES
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4
- K. L. Deak, R. J.L.F Lemmers, J. M. Stajich, R. Klooster, R. Tawil, R. R. Frants, M. C. Speer, S. M. van der Maarel, and J. R. Gilbert
Neurology 2007; 68: 578-582.
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- EDITORIALS
Muscle biopsy in patients with myalgia: Still a painful decision
- John T. Kissel
Neurology 2007; 68: 170-171.
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- ARTICLES
The role of muscle biopsy in investigating isolated muscle pain
- M. Filosto, P. Tonin, G. Vattemi, L. Bertolasi, A. Simonati, N. Rizzuto, and G. Tomelleri
Neurology 2007; 68: 181-186.
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- ARTICLES
Outcome of noninvasive ventilation in children with neuromuscular disease
- H. K. Young, A. Lowe, D. A. Fitzgerald, C. Seton, K. A. Waters, E. Kenny, L. S. Hynan, S. T. Iannaccone, K. N. North, and M. M. Ryan
Neurology 2007; 68: 198-201.
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