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All Neuromuscular Disease
Citations 1-10 of 158 total displayed.
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Most recent content
(24 Nov 2009):
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- CLINICAL/SCIENTIFIC NOTES
ENDPLATE DESTRUCTION DUE TO MATERNAL ANTIBODIES IN ARTHROGRYPOSIS MULTIPLEX CONGENITA
- J. Reimann, L. Jacobson, A. Vincent, and C. Kornblum
Neurology 2009; 73: 1806-1808.
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Past content
(since Jan 2000):
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- EDITORIALS
Another gene for ALS: Mutations in sporadic cases and the rare variant hypothesis
- Kevin Talbot
Neurology 2009; 73: 1172-1173.
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- ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
- V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J. -P. Bouchard, L. Lacomblez, F. Salachas, P. -F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology 2009; 73: 1176-1179.
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- CLINICAL/SCIENTIFIC NOTES
CORE-ROD MYOPATHY CAUSED BY MUTATIONS IN THE NEBULIN GENE
- N. B. Romero, V. -L. Lehtokari, S. Quijano-Roy, N. Monnier, K. G. Claeys, R. Y. Carlier, N. Pellegrini, D. Orlikowski, A. Barois, N. G. Laing, J. Lunardi, M. Fardeau, K. Pelin, and C. Wallgren-Pettersson
Neurology 2009; 73: 1159-1161.
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- CLINICAL/SCIENTIFIC NOTES
A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A
- S. Rajakulendran, S. V. Tan, E. Matthews, S. E. Tomlinson, R. Labrum, R. Sud, D. M. Kullmann, S. Schorge, and M. G. Hanna
Neurology 2009; 73: 993-995.
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- EDITORIALS
Another gene for ALS. Mutations in sporadic cases and the rare variant hypothesis
- Kevin Talbot
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bd1161.
Rapid PDF
- ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
- V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J.-P. Bouchard, L. Lacomblez, F. Salachas, P.-F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bbfeef.
[Abstract]
Rapid PDF
- ARTICLES
Neurologic abnormalities in HTLV-I– and HTLV-II–infected individuals without overt myelopathy
- H. H. Biswas, J. W. Engstrom, Z. Kaidarova, G. Garratty, J. W. Gibble, B. H. Newman, J. W. Smith, A. Ziman, J. L. Fridey, R. A. Sacher, E. L. Murphy For the HTLV Outcomes Study (HOST)
Neurology 2009; 73: 781-789.
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- CLINICAL/SCIENTIFIC NOTES
RESTLESS LEGS SYNDROME WITH PERIODIC LIMB MOVEMENTS: A POSSIBLE CAUSE OF IDIOPATHIC HYPERCKEMIA
- G. Della Marca, S. Dittoni, M. Catteruccia, R. Frusciante, F. Madia, A. Losurdo, E. Testani, C. Vollono, and S. Servidei
Neurology 2009; 73: 643-645.
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- ARTICLES
Consequences of mutations within the C terminus of the FHL1 gene
- B. Schoser, H. H. Goebel, I. Janisch, S. Quasthoff, J. Rother, M. Bergmann, W. Müller-Felber, and C. Windpassinger
Neurology 2009; 73: 543-551.
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