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Ion channel gene defects
Citations 81-90 of 93 total displayed.
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Past content
(since Aug 2001):
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- ARTICLES
Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)
- P. Labauge, L. O. Amer, M. Simonetta-Moreau, F. Attané, C. Tannier, M. Clanet, G. Castelnovo, I. An-Gourfinkel, Y. Agid, A. Brice, A. Ducros, and E. LeGuern
Neurology 2002; 58: 941-944.
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- ARTICLES
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation
- B. Abou-Khalil, Q. Ge, R. Desai, R. Ryther, A. Bazyk, R. Bailey, J. L. Haines, J. S. Sutcliffe, and A. L. George, Jr.
Neurology 2001; 57: 2265-2272.
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- ARTICLES
Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission
- J. Jen, J. Wan, M. Graves, H. Yu, A. F. Mock, C. J. Coulin, G. Kim, Q. Yue, D. M. Papazian, and R. W. Baloh
Neurology 2001; 57: 1843-1848.
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- ARTICLES
Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative
- J.-F. Desaphy, A. De Luca, P. Tortorella, D. De Vito, A. L. George, Jr., and D. Conte Camerino
Neurology 2001; 57: 1849-1857.
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- BRIEF COMMUNICATIONS
Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene
- Marios Panas, Nikolaos Kalfakis, Charalampos Karadimas, and Demetris Vassilopoulos
Neurology 2001; 57: 1906-1908.
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- BRIEF COMMUNICATIONS
Persistent facial myokymia associated with K+ channel antibodies
- Ludwig Gutmann, John G. Tellers, and Steven Vernino
Neurology 2001; 57: 1707-1708.
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- BRIEF COMMUNICATIONS
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL
- Martin Dichgans, Jürgen Herzog, and Thomas Gasser
Neurology 2001; 57: 1714-1717.
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- CLINICAL/SCIENTIFIC NOTES
Familial hemiplegic migraine and its abortive therapy with intravenous verapamil
- Wengui Yu and Steven H. Horowitz
Neurology 2001; 57: 1732-1733.
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- BRIEF COMMUNICATIONS
Benign nocturnal alternating hemiplegia of childhood: Six patients and long-term follow-up
- V. Chaves–Vischer, F. Picard, E. Andermann, B. Dalla Bernardina, and F. Andermann
Neurology 2001; 57: 1491-1493.
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- BRIEF COMMUNICATIONS
An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus
- J. L. Steckley, G. C. Ebers, M. Z. Cader, and R. S. McLachlan
Neurology 2001; 57: 1499-1502.
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