Similar articles for PMID: 16217063

Year	Number of Results
1974	1
2000	1
2002	1
2003	4
2004	3
2005	8
2006	20
2007	21
2008	7
2009	5
2010	7
2011	8
2012	3
2013	7
2014	11
2015	13
2016	8
2017	6
2018	5
2019	10
2020	10
2021	7
2022	5
2023	2
2024	0

1

Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.

Davies NP, Imbrici P, Fialho D, Herd C, Bilsland LG, Weber A, Mueller R, Hilton-Jones D, Ealing J, Boothman BR, Giunti P, Parsons LM, Thomas M, Manzur AY, Jurkat-Rott K, Lehmann-Horn F, Chinnery PF, Rose M, Kullmann DM, Hanna MG. Davies NP, et al. Neurology. 2005 Oct 11;65(7):1083-9. doi: 10.1212/01.wnl.0000178888.03767.74. Neurology. 2005. PMID: 16217063

2

T75M-KCNJ2 mutation causing Andersen-Tawil syndrome enhances inward rectification by changing Mg2+ sensitivity.

Tani Y, Miura D, Kurokawa J, Nakamura K, Ouchida M, Shimizu K, Ohe T, Furukawa T. Tani Y, et al. J Mol Cell Cardiol. 2007 Aug;43(2):187-96. doi: 10.1016/j.yjmcc.2007.05.005. Epub 2007 May 18. J Mol Cell Cardiol. 2007. PMID: 17582433

3

A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.

Chan HF, Chen ML, Su JJ, Ko LC, Lin CH, Wu RM. Chan HF, et al. J Hum Genet. 2010 Mar;55(3):186-8. doi: 10.1038/jhg.2010.2. Epub 2010 Jan 29. J Hum Genet. 2010. PMID: 20111058

4

Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome.

Ballester LY, Benson DW, Wong B, Law IH, Mathews KD, Vanoye CG, George AL Jr. Ballester LY, et al. Hum Mutat. 2006 Apr;27(4):388. doi: 10.1002/humu.9418. Hum Mutat. 2006. PMID: 16541386

5

Andersen cardiodysrhythmic periodic paralysis with KCNJ2 mutations: a novel mutation in the pore selectivity filter residue.

Lim BC, Kim GB, Bae EJ, Noh CI, Hwang H, Kim KJ, Hwang YS, Ko TS, Chae JH. Lim BC, et al. J Child Neurol. 2010 Apr;25(4):490-3. doi: 10.1177/0883073809357937. J Child Neurol. 2010. PMID: 20382953

6

Phenotype variability in patients carrying KCNJ2 mutations.

Kimura H, Zhou J, Kawamura M, Itoh H, Mizusawa Y, Ding WG, Wu J, Ohno S, Makiyama T, Miyamoto A, Naiki N, Wang Q, Xie Y, Suzuki T, Tateno S, Nakamura Y, Zang WJ, Ito M, Matsuura H, Horie M. Kimura H, et al. Circ Cardiovasc Genet. 2012 Jun;5(3):344-53. doi: 10.1161/CIRCGENETICS.111.962316. Epub 2012 May 15. Circ Cardiovasc Genet. 2012. PMID: 22589293

7

Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.

Limberg MM, Zumhagen S, Netter MF, Coffey AJ, Grace A, Rogers J, Böckelmann D, Rinné S, Stallmeyer B, Decher N, Schulze-Bahr E. Limberg MM, et al. Basic Res Cardiol. 2013 May;108(3):353. doi: 10.1007/s00395-013-0353-1. Epub 2013 May 5. Basic Res Cardiol. 2013. PMID: 23644778

8

Andersen-Tawil syndrome: definition of a neurocognitive phenotype.

Yoon G, Quitania L, Kramer JH, Fu YH, Miller BL, Ptácek LJ. Yoon G, et al. Neurology. 2006 Jun 13;66(11):1703-10. doi: 10.1212/01.wnl.0000218214.64942.64. Neurology. 2006. PMID: 16769944 Clinical Trial.

9

Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.

Zhang L, Benson DW, Tristani-Firouzi M, Ptacek LJ, Tawil R, Schwartz PJ, George AL, Horie M, Andelfinger G, Snow GL, Fu YH, Ackerman MJ, Vincent GM. Zhang L, et al. Circulation. 2005 May 31;111(21):2720-6. doi: 10.1161/CIRCULATIONAHA.104.472498. Epub 2005 May 23. Circulation. 2005. PMID: 15911703

10

A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndrome.

Doi T, Makiyama T, Morimoto T, Haruna Y, Tsuji K, Ohno S, Akao M, Takahashi Y, Kimura T, Horie M. Doi T, et al. Circ Cardiovasc Genet. 2011 Jun;4(3):253-60. doi: 10.1161/CIRCGENETICS.110.958157. Epub 2011 Apr 14. Circ Cardiovasc Genet. 2011. PMID: 21493816

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