Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Epilepsy and CHRNA4[original query] |
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Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes. Epilepsy research 2002 Dec 52 (2): 107-16. Chioza B, Osei-Lah A, Wilkie H, Nashef L, McCormick D, Asherson P, Makoff A |
Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions. Epilepsia 2003 Aug 44 (8): 1089-93. Chou I-Ching, Lee Cheng-Chun, Huang Chao-Ching, Wu Jer-Yuarn, Tsai Jeffrey J P, Tsai Chang-Hai, Tsai Fuu-J |
Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children. Journal of biomedical science 2005 Oct 12 (5): 815-8. Haider M Z, Habeeb Y, Al-Nakkas E, Al-Anzi H, Zaki M, Al-Tawari A, Al-Bloushi |
A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely. Neuroscience letters 2007 Jul 422 (1): 74-6. Gu Wenli, Bertrand Daniel, Steinlein Ortrud |
Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits. Journal of clinical laboratory analysis 2007 21 (2): 67-70. Lee Cheng-Chun, Chou I-Ching, Tsai Chang-Hai, Wan Lei, Shu Yu-An, Tsai Yuhsin, Li Tsai-Chung, Tsai Fuu-J |
A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy. Epilepsy research 2009 Feb 83 (2-3): 152-6. Chen Yan, Wu Liwen, Fang Yue, He Zhiyi, Peng Bingwei, Shen Yan, Xu |
CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients. Sleep medicine 2009 Jan 10 (1): 139-42. Combi Romina, Ferini-Strambi Luigi, Tenchini Maria Lui |
The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy. Seizure 2009 Oct 18 (8): 601-3. Rozycka Agata, Steinborn Barbara, Trzeciak Wieslaw |
The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy. Epilepsy research 2011 Jun 95 (1-2): 94-9. Liu Hui, Lu Cailing, Li Zhenzhong, Zhou Shiyi, Li Xiaoqiao, Ji Liri, Lu Qiang, Lv Ruijuan, Wu Liwen, Ma |
[Clinical features and mutation analysis of CHRNA4 gene for families and sporadic cases affected with autosomal dominant nocturnal frontal lobe epilepsy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2013 Dec 30 (6): 662-5. Zhai Qiong-xiang, Wang Chun, Chen Qian, Guo Yu-xiong, Chen Zhi-hong, Zhang Yu-xin, Gui Juan, Tang Zhi-hong, Zhuo Mu-qi |
Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy. International journal of clinical and experimental medicine 2015 8 (6): 9063-70. Chen Zhihong, Wang Lingan, Wang Chun, Chen Qian, Zhai Qiongxiang, Guo Yuxiong, Zhang Yux |
Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy. CNS & neurological disorders drug targets 2015 14 (4): 468-75. Faheem Muhammad, Naseer Muhammad I, Chaudhary Adeel G, Kumosani Taha A, Rasool Mahmood, Algahtani Hussein A, Bibi Fehmida, Kamal Mohammad A, Al-Qahtani Mohammad |
Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel. Frontiers in neurology 2018 7 9 515. Tsai Meng-Han, Chan Chung-Kin, Chang Ying-Chao, Lin Chih-Hsiang, Liou Chia-Wei, Chang Wen-Neng, Ng Ching-Ching, Lim Kheng-Seang, Hwang Daw-Ya |
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients. Seizure 2019 12 74 60-64. Licchetta Laura, Pippucci Tommaso, Baldassari Sara, Minardi Raffaella, Provini Federica, Mostacci Barbara, Plazzi Giuseppe, Tinuper Paolo, Bisulli Francesca, |
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- Page last updated:Apr 22, 2024
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