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Muscle disease
Citations 211-220 of 281 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome
- Marco Crimi, Sara Galbiati, Isabella Moroni, Andreina Bordoni, Maria Paola Perini, Eleonora Lamantea, Monica Sciacco, Massimo Zeviani, Ida Biunno, Maurizio Moggio, Guglielmo Scarlato, and Giacomo Pietro Comi
Neurology 2003; 60: 1857-1861.
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- ARTICLES
Hereditary inclusion body myopathy: The Middle Eastern genetic cluster
- Z. Argov, I. Eisenberg, G. Grabov–Nardini, M. Sadeh, I. Wirguin, D. Soffer, and S. Mitrani–Rosenbaum
Neurology 2003; 60: 1519-1523.
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- CLINICAL/SCIENTIFIC NOTES
Acute necrotizing encephalopathy of childhood with radiographic progression over 10 hours
- Alexander G. Bassuk, Delilah M. Burrowes, and Wes McRae
Neurology 2003; 60: 1552-1553.
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- EDITORIALS
The limb-girdle muscular dystrophies: Genetic and phenotypic definition of a disputed entity
- Matthew P. Wicklund and David Hilton-Jones
Neurology 2003; 60: 1230-1231.
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- ARTICLES
The phenotype of limb-girdle muscular dystrophy type 2I
- M. Poppe, L. Cree, J. Bourke, M. Eagle, L.V.B. Anderson, D. Birchall, M. Brockington, M. Buddles, M. Busby, F. Muntoni, A. Wills, and K. Bushby
Neurology 2003; 60: 1246-1251.
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- BRIEF COMMUNICATIONS
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I
- A. Driss, S. Noguchi, R. Amouri, M. Kefi, T. Sasaki, K. Sugie, S. Souilem, Y.K. Hayashi, N. Shimizu, S. Minoshima, J. Kudoh, F. Hentati, and I. Nishino
Neurology 2003; 60: 1341-1344.
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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
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
- A. Agostino, L. Valletta, P.F. Chinnery, G. Ferrari, F. Carrara, R.W. Taylor, A.M. Schaefer, D.M. Turnbull, V. Tiranti, and M. Zeviani
Neurology 2003; 60: 1354-1356.
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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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- BRIEF COMMUNICATIONS
Reversion of mtDNA depletion in a patient with TK2 deficiency
- M.R. Vilà, T. Segovia-Silvestre, J. Gámez, A. Marina, A.B. Naini, A. Meseguer, A. Lombès, E. Bonilla, S. DiMauro, M. Hirano, and A.L. Andreu
Neurology 2003; 60: 1203-1205.
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