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• W1545757400 abstract "Pediatrics InternationalVolume 53, Issue 3 p. 415-416 New mutation of CACNA1A gene in episodic ataxia type 2 Koki Nikaido, Corresponding Author Koki Nikaido Department of Pediatrics, Sapporo Medical University School of MedicineKoki Nikaido, MD, PhD, Department of Pediatrics, Sapporo Medical University School of Medicine, South-1 West-16 Chuo-ku, Sapporo 060-8543, Japan. Email: [email protected]Search for more papers by this authorNobutada Tachi, Nobutada Tachi School of Health Science, SapporoSearch for more papers by this authorKazuhiro Ohya, Kazuhiro Ohya Department of Pediatrics, Sapporo Medical University School of MedicineSearch for more papers by this authorTakahito Wada, Takahito Wada Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto, JapanSearch for more papers by this authorHiroyuki Tsutsumi, Hiroyuki Tsutsumi Department of Pediatrics, Sapporo Medical University School of MedicineSearch for more papers by this author Koki Nikaido, Corresponding Author Koki Nikaido Department of Pediatrics, Sapporo Medical University School of MedicineKoki Nikaido, MD, PhD, Department of Pediatrics, Sapporo Medical University School of Medicine, South-1 West-16 Chuo-ku, Sapporo 060-8543, Japan. Email: [email protected]Search for more papers by this authorNobutada Tachi, Nobutada Tachi School of Health Science, SapporoSearch for more papers by this authorKazuhiro Ohya, Kazuhiro Ohya Department of Pediatrics, Sapporo Medical University School of MedicineSearch for more papers by this authorTakahito Wada, Takahito Wada Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto, JapanSearch for more papers by this authorHiroyuki Tsutsumi, Hiroyuki Tsutsumi Department of Pediatrics, Sapporo Medical University School of MedicineSearch for more papers by this author First published: 23 June 2011 https://doi.org/10.1111/j.1442-200X.2011.03390.xCitations: 3Read the full textAboutPDF 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 No abstract is available for this article. References 1 Tomlinson SE, Hanna MG, Kullmann DM, Veronica Tan S, Burke D. Clinical neurophysiology of the episodic ataxias: Insights into ion channel dysfunction in vivo. Clin. Neurophysiol. 2009; 120: 1768– 76. 2 Griggs RC, Moxley RT, Lafrance R. Hereditary paroxysmal ataxia: Response to acetazolamide. Neurology 1978; 28: 1259– 64. 3 Ophoff RA, Terwindt GM, Vergouwe MN et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996; 87: 543– 52. 4 Wada T, Kobayashi N, Takahashi Y, Aoki T, Watanabe T, Saitoh S. Wide clinical variability in a family with a CACNA1A T666M mutation: Hemiplegic migraine, coma, and progressive ataxia. Pediatr. Neurol. 2002; 26: 47– 50. Citing Literature Volume53, Issue3June 2011Pages 415-416 ReferencesRelatedInformation" @default.
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