Similar articles for PMID: 24849934

Year	Number of Results
1987	1
1991	1
2002	2
2003	1
2004	2
2005	3
2006	11
2007	9
2009	2
2010	6
2011	6
2012	6
2013	8
2014	11
2015	10
2016	7
2017	8
2018	5
2019	7
2020	8
2021	9
2022	8
2023	3
2024	0

1

Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosis.

Díaz-Manera J, Querol L, Alejaldre A, Rojas-García R, Ramos-Fransi A, Gallardo E, Illa I. Díaz-Manera J, et al. J Hum Genet. 2014 Aug;59(8):465-6. doi: 10.1038/jhg.2014.43. Epub 2014 May 22. J Hum Genet. 2014. PMID: 24849934

2

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis.

Li X, Yao S, Xiang Y, Zhang X, Wu X, Luo L, Huang H, Zhu M, Wan H, Hong D. Li X, et al. BMC Neurol. 2015 Mar 21;15:38. doi: 10.1186/s12883-015-0290-8. BMC Neurol. 2015. PMID: 25885757 Free PMC article.

3

Andersen-Tawil syndrome with early fixed myopathy.

Lefter S, Hardiman O, Costigan D, Lynch B, McConville J, Hand CK, Ryan AM. Lefter S, et al. J Clin Neuromuscul Dis. 2014 Dec;16(2):79-82. doi: 10.1097/CND.0000000000000052. J Clin Neuromuscul Dis. 2014. PMID: 25415519

4

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.

Cheung CL, Lau KS, Ho AY, Lee KK, Tiu SC, Lau EY, Leung J, Tsang MW, Chan KW, Yeung CY, Woo YC, Cheung EY, Hung VH, Pang HK, Hung CS, Sham PC, Kung AW. Cheung CL, et al. Nat Genet. 2012 Sep;44(9):1026-9. doi: 10.1038/ng.2367. Epub 2012 Aug 5. Nat Genet. 2012. PMID: 22863731

5

Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.

Ördög B, Hategan L, Kovács M, Seprényi G, Kohajda Z, Nagy I, Hegedűs Z, Környei L, Jost N, Katona M, Szekeres M, Forster T, Papp JG, Varró A, Sepp R. Ördög B, et al. Can J Physiol Pharmacol. 2015 Jul;93(7):569-75. doi: 10.1139/cjpp-2014-0527. Epub 2015 Apr 17. Can J Physiol Pharmacol. 2015. PMID: 26103554

6

Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2.

Modoni A, Bianchi ML, Vitulano N, Pagliarani S, Perna F, Sanna T, Rizzo V, Silvestri G. Modoni A, et al. Cardiology. 2011;120(4):200-3. doi: 10.1159/000335529. Epub 2012 Jan 26. Cardiology. 2011. PMID: 22286118

7

Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry.

Barajas-Martinez H, Hu D, Ontiveros G, Caceres G, Desai M, Burashnikov E, Scaglione J, Antzelevitch C. Barajas-Martinez H, et al. Circ Cardiovasc Genet. 2011 Feb;4(1):51-7. doi: 10.1161/CIRCGENETICS.110.957696. Epub 2010 Dec 10. Circ Cardiovasc Genet. 2011. PMID: 21148745 Free PMC article.

8

A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.

Kokunai Y, Nakata T, Furuta M, Sakata S, Kimura H, Aiba T, Yoshinaga M, Osaki Y, Nakamori M, Itoh H, Sato T, Kubota T, Kadota K, Shindo K, Mochizuki H, Shimizu W, Horie M, Okamura Y, Ohno K, Takahashi MP. Kokunai Y, et al. Neurology. 2014 Mar 25;82(12):1058-64. doi: 10.1212/WNL.0000000000000239. Epub 2014 Feb 26. Neurology. 2014. PMID: 24574546

9

Sudden cardiac death in Andersen-Tawil syndrome.

Peters S, Schulze-Bahr E, Etheridge SP, Tristani-Firouzi M. Peters S, et al. Europace. 2007 Mar;9(3):162-6. doi: 10.1093/europace/eul188. Epub 2007 Feb 1. Europace. 2007. PMID: 17272325

10

Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome.

Fukumura S, Yamauchi K, Kawanabe A, Yamamoto A, Nakaza M, Kubota T, Kato S, Sasaki R, Okamura Y, Takahashi MP. Fukumura S, et al. J Neurol Sci. 2019 Dec 15;407:116521. doi: 10.1016/j.jns.2019.116521. Epub 2019 Oct 15. J Neurol Sci. 2019. PMID: 31669729

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