Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Hypokalemic Periodic Paralysis and SCN4A[original query] |
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Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid : official journal of the American Thyroid Association 2004 Mar 14 (3): 187-90. Ng WY, Lui KF, Thai AC, Cheah JS |
Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A. Journal of pediatric endocrinology & metabolism : JPEM 2005 1 17 (12): 1679-82. Lane Andrew H, Markarian Katherine, Braziunene Ie |
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype. Neurology 2011 Nov 77 (22): 1960-4. Matthews E, Portaro S, Ke Q, Sud R, Haworth A, Davis M B, Griggs R C, Hanna M |
Mutations of SCN4A gene cause different diseases: 2 case reports and literature review. Channels (Austin, Tex.) 2015 9 (2): 82-7. Liu Xiao-li, Huang Xiao-jun, Luan Xing-hua, Zhou Hai-yan, Wang Tian, Wang Jing-yi, Chen Sheng-di, Tang Hui-dong, Cao |
Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. Neurology 2016 Mar . Song I-Wen, Sung Chih-Chien, Chen Chien-Hsiun, Cheng Chih-Jen, Yang Sung-Sen, Chou Yi-Chun, Yang Jenn-Hwai, Chen Yuan-Tsong, Wu Jer-Yuarn, Lin Shih-H |
Association study in Mexican patients with thyrotoxic hypokalemic periodic paralysis. Biomedical reports 2020 Oct 13 (4): 24. Bautista-Medina Mario Arturo, Gallardo-Blanco Hugo Leonid, Martinez-Garza Laura Elia, Cerda-Flores Ricardo Martin, Lavalle-Gonzalez Fernando Javier, Villarreal-Perez Jesus Zacari |
Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations. Neuromuscular disorders : NMD 2021 5 31 (9): 829-838. Sun J, Luo S, Suetterlin K J, Song J, Huang J, Zhu W, Xi J, Zhou L, Lu J, Lu J, Zhao C, Hanna M G, Männikkö R, Matthews E, Qiao |
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