Title: <i>KCNJ2</i> mutation in intractable ventricular arrhythmia with Andersen's syndrome
Abstract: Pediatrics InternationalVolume 47, Issue 2 p. 220-223 KCNJ2 mutation in intractable ventricular arrhythmia with Andersen's syndrome Tohru Takahashi, Tohru Takahashi The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSatoshi Tandai, Satoshi Tandai The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTsutomu Toki, Tsutomu Toki The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTakumi Sato, Takumi Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorShuji Eto, Shuji Eto The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorAkira Sato, Akira Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTomomi Ueda, Tomomi Ueda The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSumito Sato, Sumito Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorKouta Ichinose, Kouta Ichinose The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorEtsuro Ito, Etsuro Ito The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSusumu Yonesaka, Susumu Yonesaka The Department of Nursing, Hirosaki University School of Health Sciences, Hirosaki, JapanSearch for more papers by this author Tohru Takahashi, Tohru Takahashi The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSatoshi Tandai, Satoshi Tandai The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTsutomu Toki, Tsutomu Toki The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTakumi Sato, Takumi Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorShuji Eto, Shuji Eto The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorAkira Sato, Akira Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorTomomi Ueda, Tomomi Ueda The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSumito Sato, Sumito Sato The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorKouta Ichinose, Kouta Ichinose The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorEtsuro Ito, Etsuro Ito The Department of Pediatrics, Hirosaki University School of MedicineSearch for more papers by this authorSusumu Yonesaka, Susumu Yonesaka The Department of Nursing, Hirosaki University School of Health Sciences, Hirosaki, JapanSearch for more papers by this author First published: 16 March 2005 https://doi.org/10.1111/j.1442-200x.2005.02024.xCitations: 5 Tohru Takahashi, Department of Pediatrics, Hirosaki University School of Medicine, 5 Zaifu-tyo, Hirosaki 036-8562, Japan. Email: [email protected] Read 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 Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Andersen ED, Krasilnikoff PA, Overvad H. Intermittent muscular weakness, extrasystole, and multiple developmental abnormalities: a new syndrome? Acta Paedriatr. Scand. 1971; 60: 559 – 64. 2 Tawil R, Ptacek LJ, Pavlakis SG et al. Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. Ann. Neurol. 1994; 35: 326 – 30. 3 Plaster NM, Tawil R, Tristani-Firouzi M et al. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Cell 2001; 105: 511 – 19. 4 Eldar M, Griffin JC, Van Hare GF et al. Combined use of beta-adrenergic blocking agents and long-term cardiac pacing for patients with the long QT syndrome. J. Am. Coll. Cardiol. 1992; 20: 830 – 7. 5 Shimizu W, Kurita T, Matsuo K et al. Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome. Circulation 1998; 97: 1581 – 8. 6 Tristani-Firouzi M, Jensen JL, Donaldson MR et al. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). J. Clin. Invest. 2002; 110: 381 – 8. 7 Lopatin AN, Nichols CG. Inward rectifiers in the heart: an update on IK1. J. Mol. Cell. Cardiol. 2001; 33: 625 – 38. 8 Jongsma HJ, Wilders R. Channelopathies: Kir2.1 mutations jeopardize many cell functions. Curr. Biol. 2001; 11: R747 – 50. 9 Donaldson MR, Jensen JL, Tristani-Firouzi M et al. PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. Neurology 2003; 60: 1811 – 16. 10 Junker J, Haverkamp W, Schulze-Bahr E et al. Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome. Neurology 2002; 59: 466. Citing Literature Volume47, Issue2April 2005Pages 220-223 ReferencesRelatedInformation
Publication Year: 2005
Publication Date: 2005-03-16
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 8
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