Similar articles for PMID: 28106564

Year	Number of Results
2005	3
2006	11
2007	8
2008	2
2009	4
2010	8
2011	6
2012	6
2013	7
2014	15
2015	13
2016	5
2017	5
2018	2
2019	7
2020	10
2021	7
2022	3
2023	1
2024	0

1

Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases.

Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G. Oz Tuncer G, et al. J Neuromuscul Dis. 2017;4(1):93-95. doi: 10.3233/JND-160188. J Neuromuscul Dis. 2017. PMID: 28106564 No abstract available.

2

A Girl with Palpitations and Periodic Weakness.

Samanta D. Samanta D. Indian J Pediatr. 2019 May;86(5):480. doi: 10.1007/s12098-019-02863-1. Epub 2019 Jan 18. Indian J Pediatr. 2019. PMID: 30656561 No abstract available.

3

A study supporting possible expression of inward-rectifying potassium channel 2.1 channels in peripheral nerve in a patient with Andersen-Tawil syndrome.

Shibuya K, Tsuneyama A, Beppu M, Misawa S, Sekiguchi Y, Amino H, Suzuki YI, Suichi T, Nakamura K, Kuwabara S. Shibuya K, et al. Muscle Nerve. 2019 Apr;59(4):E28-E30. doi: 10.1002/mus.26430. Epub 2019 Feb 8. Muscle Nerve. 2019. PMID: 30681175 No abstract available.

4

A family with Andersen-Tawil syndrome and dilated cardiomyopathy.

Schoonderwoerd BA, Wiesfeld AC, Wilde AA, van den Heuvel F, Van Tintelen JP, van den Berg MP, Van Veldhuisen DJ, Van Gelder IC. Schoonderwoerd BA, et al. Heart Rhythm. 2006 Nov;3(11):1346-50. doi: 10.1016/j.hrthm.2006.07.021. Epub 2006 Jul 21. Heart Rhythm. 2006. PMID: 17074642 No abstract available.

5

Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.

Liu XL, Huang XJ, Luan XH, Zhou HY, Wang T, Wang JY, Shen JY, Chen SD, Tang HD, Cao L. Liu XL, et al. J Neurol Sci. 2015 May 15;352(1-2):105-6. doi: 10.1016/j.jns.2015.02.027. Epub 2015 Feb 20. J Neurol Sci. 2015. PMID: 25847018 No abstract available.

6

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

7

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

8

Vanishing Weakness and Persistent Cardiac Dysrhythmia: Are We Dealing with Andersen Tawil Syndrome?

Jhansi Rani P, Yashodhara P, Sundarachary NV, Veeramma U, Elahi SM, Amalakanti S, Lalitha A. Jhansi Rani P, et al. Indian J Pediatr. 2015 Jul;82(7):642-4. doi: 10.1007/s12098-014-1677-z. Epub 2015 Jan 25. Indian J Pediatr. 2015. PMID: 25616308

9

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

10

Neurophysiologic characterization of periodic paralysis episode in a patient with Andersen-Tawil syndrome.

Falcão de Campos C, de Carvalho M. Falcão de Campos C, et al. Clin Neurophysiol. 2018 Mar;129(3):558-559. doi: 10.1016/j.clinph.2017.12.033. Epub 2018 Jan 4. Clin Neurophysiol. 2018. PMID: 29353185 No abstract available.

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