Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Epilepsy and CACNA1H[original query] |
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Association between genetic variation of CACNA1H and childhood absence epilepsy. Annals of neurology 2003 Aug 54 (2): 239-43. Chen Yucai, Lu Jianjun, Pan Hong, Zhang Yuehua, Wu Husheng, Xu Keming, Liu Xiaoyan, Jiang Yuwu, Bao Xinhua, Yao Zhijian, Ding Keyue, Lo Wilson H Y, Qiang Boqin, Chan Piu, Shen Yan, Wu Xi |
Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy. The Journal of biological chemistry 2004 1 279 (11): 9681-4. Khosravani Houman, Altier Christophe, Simms Brett, Hamming Kevin S, Snutch Terrance P, Mezeyova Janette, McRory John E, Zamponi Gerald |
Common polymorphisms in the CACNA1H gene associated with childhood absence epilepsy in Chinese Han population. Annals of human genetics 2007 May 71 (Pt 3): 325-35. Liang J, Zhang Y, Chen Y, Wang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu |
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants. Annals of neurology 2007 Dec 62 (6): 560-8. Heron Sarah E, Khosravani Houman, Varela Diego, Bladen Chris, Williams Tristiana C, Newman Michelle R, Scheffer Ingrid E, Berkovic Samuel F, Mulley John C, Zamponi Gerald |
Association study between polymorphisms in the CACNA1A, CACNA1C, and CACNA1H genes and drug-resistant epilepsy in the Chinese Han population. Seizure 2015 Aug 30 64-9. Lv Nan, Qu Jian, Long Hongyu, Zhou Luo, Cao Yuze, Long Lili, Liu Zhaoqian, Xiao |
Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy. Annals of neurology 2017 Mar 81 (3): 444-453. Glauser Tracy A, Holland Katherine, O'Brien Valerie P, Keddache Mehdi, Martin Lisa J, Clark Peggy O, Cnaan Avital, Dlugos Dennis, Hirtz Deborah G, Shinnar Shlomo, Grabowski Gregory, |
Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes. Neurogenetics 2018 6 19 (3): 165-178. Landoulsi Zied, Laatar Fatma, Noé Eric, Mrabet Saloua, Ben Djebara Mouna, Achaz Guillaume, Nava Caroline, Baulac Stéphanie, Kacem Imen, Gargouri-Berrechid Amina, Gouider Riadh, Leguern Er |
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes. PloS one 2018 13 (6): e0199321. Lee Cha Gon, Lee Jeehun, Lee Munhya |
Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy. Epilepsia open 2017 09 2 (3): 334-342. Becker Felicitas, Reid Christopher A, Hallmann Kerstin, Tae Han-Shen, Phillips A Marie, Teodorescu Georgeta, Weber Yvonne G, Kleefuss-Lie Ailing, Elger Christian, Perez-Reyes Edward, Petrou Steven, Kunz Wolfram S, Lerche Holger, Maljevic Sneza |
Copy number variation in fetal alcohol spectrum disorder. Biochemistry and cell biology = Biochimie et biologie cellulaire 2018 Mar 1-6. Zarrei Mehdi, Hicks Geoffrey G, Reynolds James N, Thiruvahindrapuram Bhooma, Engchuan Worrawat, Pind Molly, Lamoureux Sylvia, Wei John, Wang Zhouzhi, Marshall Christian R, Wintle Richard F, Chudley Albert E, Scherer Stephen |
The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children. Frontiers in neurology 2019 10 505. Long Shasha, Zhou Hao, Li Shuang, Wang Tianqi, Ma Yu, Li Chunpei, Zhou Yuanfeng, Zhou Shuizhen, Wu Bingbing, Wang |
The prognosis of epilepsy patients with CACNA1H missense variants: A longitudinal cohort study. Seizure 2021 May 91 52-59. Wei Zihan, Liu Chao, Wu Zhenyu, Cao Mi, Qiao Xiaozhi, Han Tenghui, Zhang Ying, Liu Yonghong, Deng Yanch |
Contribution of rare genetic variants to drug response in absence epilepsy. Epilepsy research 2021 Jan 170 106537. Myers Kenneth A, Bennett Mark F, Grinton Bronwyn E, Dabscheck Gabriel, Chan Eunice K, Bello-Espinosa Luis E, Sadleir Lynette G, D'Alfonso Sabrina, Schneider Amy L, Damiano John A, Hildebrand Michael S, Bahlo Melanie, Berkovic Samuel F, Buchhalter Jeffrey, Scheffer Ingrid |
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- Page last updated:Apr 22, 2024
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