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Ion channel gene defects
Citations 51-60 of 93 total displayed.
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Past content
(since Aug 2001):
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- BRIEF COMMUNICATIONS
Elicited repetitive daily blindness: A new familial disorder related to migraine and epilepsy
- D. Le Fort, A.B. Safran, F. Picard, I. Bouchardy, and M.A. Morris
Neurology 2004; 63: 348-350.
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- ARTICLES
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
- R. Borgatti, C. Zucca, A. Cavallini, M. Ferrario, C. Panzeri, P. Castaldo, M. V. Soldovieri, C. Baschirotto, N. Bresolin, B. Dalla Bernardina, M. Taglialatela, and M. T. Bassi
Neurology 2004; 63: 57-65.
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- CLINICAL/SCIENTIFIC NOTES
Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A
- S. Pereira, J. P. Vieira, F. Barroca, P. Roll, R. Carvalhas, P. Cau, S. Sequeira, P. Genton, and P. Szepetowski
Neurology 2004; 63: 191-192.
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- BRIEF COMMUNICATIONS
Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine
- M. Strupp, R. Kalla, M. Dichgans, T. Freilinger, S. Glasauer, and T. Brandt
Neurology 2004; 62: 1623-1625.
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- EDITORIALS
Autoantibodies in the CNS: Encephalopathy and potassium channelopathy
- David Beeson
Neurology 2004; 62: 1040-1041.
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- ARTICLES
Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome
- R. Webster, M. Brydson, R. Croxen, J. Newsom–Davis, A. Vincent, and D. Beeson
Neurology 2004; 62: 1090-1096.
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- ARTICLES
Potentially reversible autoimmune limbic encephalitis with neuronal potassium channel antibody
- M. J. Thieben, V. A. Lennon, B. F. Boeve, A. J. Aksamit, M. Keegan, and S. Vernino
Neurology 2004; 62: 1177-1182.
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- BRIEF COMMUNICATIONS
Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation
- Karin Jurkat-Rott and Frank Lehmann-Horn
Neurology 2004; 62: 1012-1015.
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- CLINICAL/SCIENTIFIC NOTES
Benign alternating hemiplegia of childhood: New features and associations
- Megan Kavanaugh and Gary J. Myers
Neurology 2004; 62: 672.
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- ARTICLES
Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2
- R.A. Maselli, J. Wan, V. Dunne, M. Graves, R.W. Baloh, R.L. Wollmann, and J. Jen
Neurology 2003; 61: 1743-1748.
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