|
Ion channel gene defects
Citations 31-40 of 93 total displayed.
|
Past content
(since Aug 2001):
|
- BRIEF COMMUNICATIONS
Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia
- S. D. Spacey, P. J. Adams, P.C.P. Lam, L. A. Materek, A. J. Stoessl, T. P. Snutch, and G. -Y.R. Hsiung
Neurology 2006; 66: 1588-1590.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Small vessel abnormalities in alternating hemiplegia of childhood: Pathophysiologic implications
- S. Auvin, S. Joriot-Chekaf, J. C. Cuvellier, F. Pandit, J. M. Cuisset, M. M. Ruchoux, and L. Vallée
Neurology 2006; 66: 499-504.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene
- H. Jungbluth, H. Zhou, L. Hartley, B. Halliger-Keller, S. Messina, C. Longman, M. Brockington, S. A. Robb, V. Straub, T. Voit, M. Swash, A. Ferreiro, G. Bydder, C. A. Sewry, C. Müller, and F. Muntoni
Neurology 2005; 65: 1930-1935.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Andersen–Tawil syndrome: New potassium channel mutations and possible phenotypic variation
- N. P. Davies, P. Imbrici, D. Fialho, C. Herd, L. G. Bilsland, A. Weber, R. Mueller, D. Hilton-Jones, J. Ealing, B. R. Boothman, P. Giunti, L. M. Parsons, M. Thomas, A. Y. Manzur, K. Jurkat-Rott, F. Lehmann-Horn, P. F. Chinnery, M. Rose, D. M. Kullmann, and M. G. Hanna
Neurology 2005; 65: 1083-1089.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures
- J. C. Jen, J. Wan, T. P. Palos, B. D. Howard, and R. W. Baloh
Neurology 2005; 65: 529-534.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
New calcium channel mutations predict aberrant RNA splicing in episodic ataxia
- Louise H. Eunson, Tracey D. Graves, and Michael G. Hanna
Neurology 2005; 65: 308-310.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia
- M. Z. Cader, J. L. Steckley, D. A. Dyment, R. S. McLachlan, and G. C. Ebers
Neurology 2005; 65: 156-158.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II
- J. P. Dreier, K. Jurkat-Rott, G. C. Petzold, O. Tomkins, R. Klingebiel, U. A. Kopp, F. Lehmann-Horn, A. Friedman, and M. Dichgans
Neurology 2005; 64: 2145-2147.
[Abstract]
[Full text]
[PDF]
- CORRECTIONS
Correction
-
Neurology 2005; 64: 2147.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotonia
- C. Antozzi, C. Frassoni, A. Vincent, M. C. Regondi, F. Andreetta, P. Bernasconi, C. Ciano, T. Chang, F. Cornelio, R. Spreafico, and R. Mantegazza
Neurology 2005; 64: 1290-1293.
[Abstract]
[Full text]
[PDF]
|
|
