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Episodic ataxias as channelopathies

1995; Wiley; Volume: 37; Issue: 3 Linguagem: Inglês

10.1002/ana.410370302

1531-8249

Robert C. Griggs, John G. Nutt,

Autoimmune Neurological Disorders and Treatments

Annals of NeurologyVolume 37, Issue 3 p. 285-287 Editorial Episodic ataxias as channelopathies Robert C. Griggs MD, Robert C. Griggs MD Department of Neurology University of Rochester School of Medicine and Dentistry Rochester, NYSearch for more papers by this authorJohn G. Nutt MD, John G. Nutt MD Department of Neurology Oregon Health Sciences University Portland, ORSearch for more papers by this author Robert C. Griggs MD, Robert C. Griggs MD Department of Neurology University of Rochester School of Medicine and Dentistry Rochester, NYSearch for more papers by this authorJohn G. Nutt MD, John G. Nutt MD Department of Neurology Oregon Health Sciences University Portland, ORSearch for more papers by this author First published: March 1995 https://doi.org/10.1002/ana.410370302Citations: 98AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Vahedi, K. Joutel, A. Van Bogaert, P. et al. A gene for hereditarty paroxysmal cerebellar ataxia maps to chromosome 19p. Ann Neurol 1995; 37: 289–293 2 Gancher ST, Nutt JG. Autosomal dominant episodic ataxia: a heterogeneous syndrome. Mov Dis 1986; 1: 239–253 3 Brunt EP, Van Weerden, TW. Familial paroxysmal kinesigenic ataxia and continuous myokymia. Brain 1990; 113: 1361–1382 4 Browne DL, Gancher ST, Nutt JG, et al. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genet 1994; 8: 136–140 5 Litt, M. Kramer, P. Browne, D. et al. A gene for episodic ataxia/myokymia maps to chromosome 12p13. Am J Hum Genet 1994; 55: 702–709 6 Tournier-Lasserve, E. Joutel, A. Melki, J. et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy maps to chromosome 19q12. Nature Genet 1993; 3: 256–259 7 Kramer PL, Smith, E. Carrero-Valenzuela, et al. A gene for nystagmus-associated episodic ataxia maps to chromosome 19p. Am J Hum Genet 1994; 55 (suppl): A191 8 Griggs RC, Moxley RT, Lafrance RA, McQuillen J. Hereditary paroxysmal ataxia: response to acetazolamide. Neurology 1978; 12: 1259–1264 9 Bain PG, O'Brien MD, Keevil SF, Porter DA. Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis. Ann Neurol 1992; 31: 147–154 10 Ptáĉek LJ, Johnson KJ, Griggs RC. Mechanisms of disease: genetics and physiology of the myotonic muscle disorders. N Engl J Med 1993; 328: 482–489 11 Ptáĉek LJ, Tawil, R. Griggs RC, et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994; 77: 863–868 Citing Literature Volume37, Issue3March 1995Pages 285-287 ReferencesRelatedInformation