Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Seizures and CACNA1H[original query] |
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| 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 |
| 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 |
| 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 |
| Comparative Analysis of Lennox-Gastaut Syndrome With Different Subtypes of Tonic Seizures: A Single-Center Retrospective Cohort Study. Pediatric neurology 2024 10 161 132-138. Shiyu Wang, Xuan Zhao, Ting Li, Yu Jia, Liping Zhang, Xiaohong Qi, Yicong Lin, Yuping Wa |
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