Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Epilepsy and RELN[original query] |
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An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal. Cellular and molecular neurobiology 2011 Jan 31 (1): 45-56. Dutta Shruti, Gangopadhyay Prasanta K, Sinha Swagata, Chatterjee Anindita, Ghosh Saurabh, Rajamma Us |
SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus. Epileptic disorders : international epilepsy journal with videotape 2019 4 21 (2): 185-191. Bisulli Francesca, Licchetta Laura, Baldassari Sara, Muccioli Lorenzo, Marconi Caterina, Cantalupo Gaetano, Myers Candace, Menghi Veronica, Minardi Raffaella, Caporali Leonardo, Marini Carla, Guerrini Renzo, Mefford Heather C, Tinuper Paolo, Pippucci Tomma |
The Study of Genetic Susceptibility and Mitochondrial Dysfunction in Mesial Temporal Lobe Epilepsy. Molecular neurobiology 2020 7 57 (9): 3920-3930. Yang Haiyan, Yin Fei, Gan Siyi, Pan Zou, Xiao Ting, Kessi Miriam, Yang Zhuangyi, Zhang Victor Wei, Wu Liw |
Epilepsy with auditory features: Contribution of known genes in 112 patients. Seizure 2021 1 85 115-118. Bisulli F, Rinaldi C, Pippucci T, Minardi R, Baldassari S, Zenesini C, Mostacci B, Fanella M, Avoni P, Menghi V, Caporali L, Muccioli L, Tinuper P, Licchetta |
Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy. Epileptic disorders : international epilepsy journal with videotape 2021 Jul . Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji |
Heterozygous RELN missense variants associated with genetic generalized epilepsy. Seizure 2023 8 111 122-129. Xiaoling Wu, Shaoping Zhong, Yang Cai, Yuling Yang, Yangye Lian, Jing Ding, Xin Wa |
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