HuGE Literature Finder
Records 1-6
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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 |
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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 |
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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 |
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[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 |
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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 |
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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 |
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