HuGE Literature Finder
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| A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures. Brain research 2019 7 1721 146332. Liu Feng, Du Chao, Tian Xin, Ma Yuanlin, Zhao Bei, Yan Yin, Lin Zijun, Lin Peijia, Zhou Ruijiao, Wang Xuefe |
| Factors predicting uncontrolled seizures in epilepsy with auditory features. Seizure 2019 1 65 55-61. Zhang Lin, Zhu Xi, Zou Xiaoyi, Chen L |
| 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 |
| ADGRV1 is implicated in myoclonic epilepsy. Epilepsia 2017 Dec . Myers Kenneth A, Nasioulas Steven, Boys Amber, McMahon Jacinta M, Slater Howard, Lockhart Paul, Sart Desirée du, Scheffer Ingrid |
| Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation. Epilepsy research 2015 Dec 120 73-78. Kesim Yesim F, Uzun Gunes Altiokka, Yucesan Emrah, Tuncer Feyza N, Ozdemir Ozkan, Bebek Nerses, Ozbek Ugur, Iseri Sibel A Ugur, Baykan Bet |
| Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Neuroscience letters 2008 May 436 (1): 23-6. Bovo Giorgia, Diani Erica, Bisulli Francesca, Di Bonaventura Carlo, Striano Pasquale, Gambardella Antonio, Ferlazzo Edoardo, Egeo Gabriella, Mecarelli Oriano, Elia Maurizio, Bianchi Amedeo, Bortoluzzi Stefania, Vettori Andrea, Aguglia Umberto, Binelli Simona, De Falco Arturo, Coppola Giangennaro, Gobbi Giuseppe, Sofia Vito, Striano Salvatore, Tinuper Paolo, Giallonardo Anna T, Michelucci Roberto, Nobile Car |
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