Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Hypokalemic Periodic Paralysis and CACNA1S[original query] |
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Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis. The American journal of the medical sciences 2005 Feb 329 (2): 66-70. Lin Shih-Hua, Hsu Yaw-Don, Cheng Nai-Lin, Kao Ming-Chi |
[The relationships between the single nueleotide polymorphisms of CACNA1S gene 11 exon and thyrotoxic hypokalemic periodic paralysis in the people of Han Nationality in Sichuan Province, China]. Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi 2011 Jun 28 (3): 547-52, 558. Xiao Zhu, Li Li, Li Sheyu, Yao Yu, Liu Yuping, Tian Haomi |
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 |
PharmGKB summary: very important pharmacogene information for CACNA1S. Pharmacogenetics and genomics 2019 12 30 (2): 34-44. Sangkuhl Katrin, Dirksen Robert T, Alvarellos Maria L, Altman Russ B, Klein Teri |
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 |
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- Page last updated:Sep 25, 2023
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