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Muscle disease
Citations 181-190 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Autosomal dominant hyaline body myopathy: Clinical variability and pathologic findings
- S. Bohlega, B. Lach, B. F. Meyer, Y. Al Said, M. Kambouris, M. Al Homsi, and E. J. Cupler
Neurology 2003; 61: 1519-1523.
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- EDITORIALS
Echo of silence: Silent mutations, RNA splicing, and neuromuscular diseases
- Ami Mankodi and Tetsuo Ashizawa
Neurology 2003; 61: 1330-1331.
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- BRIEF COMMUNICATIONS
Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease
- I. Fernandez-Cadenas, A.L. Andreu, J. Gamez, R. Gonzalo, M.A. Martín, J.C. Rubio, and J. Arenas
Neurology 2003; 61: 1432-1434.
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- ARTICLES
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles
- M. Wohlgemuth, R. J. Lemmers, E. L. van der Kooi, M. J. van der Wielen, P. G. van Overveld, H. Dauwerse, E. Bakker, R. R. Frants, G. W. Padberg, and S. M. van der Maarel
Neurology 2003; 61: 909-913.
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- ARTICLES
Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis
- Y. Sugiura, N. Makita, L. Li, P. J. Noble, J. Kimura, Y. Kumagai, T. Soeda, and T. Yamamoto
Neurology 2003; 61: 914-918.
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- BRIEF COMMUNICATIONS
Patients with severe muscle wasting are prone to develop hypoglycemia during fasting
- M. C. Ørngreen, M. Zacho, A. Hebert, M. Laub, and J. Vissing
Neurology 2003; 61: 997-1000.
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- BRIEF COMMUNICATIONS
Lack of association of the potassium channel–associated peptide MiRP2-R83H variant with periodic paralysis
- D. Sternberg, N. Tabti, E. Fournier, B. Hainque, and B. Fontaine
Neurology 2003; 61: 857-859.
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- CLINICAL/SCIENTIFIC NOTES
Reversible upper limb muscle weakness with selective loss of thick filaments
- G. Vattemi, P. Tonin, M. Filosto, C. Savio, N. Rizzuto, and G. Tomelleri
Neurology 2003; 61: 863-864.
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- CLINICAL/SCIENTIFIC NOTES
Autoimmune rippling muscle
- Suraj Ashok Muley and John W. Day
Neurology 2003; 61: 869-870.
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- BRIEF COMMUNICATIONS
Effect of diet on exercise tolerance in carnitine palmitoyltransferase II deficiency
- Mette C. Ørngreen, Rasmus Ejstrup, and John Vissing
Neurology 2003; 61: 559-561.
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