Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Epilepsy and LGI1[original query] |
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| 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 |
| Evaluation of depression risk in LGI1 mutation carriers. Epilepsia 2010 Sep 51 (9): 1685-90. Heiman Gary A, Kamberakis Kay, Gill Richard, Kalachikov Sergey, Pedley Timothy A, Hauser W Allen, Ottman Ru |
| Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy. Epilepsy research 2011 Mar 94 (1-2): 110-6. Busolin Giorgia, Malacrida Sandro, Bisulli Francesca, Striano Pasquale, Di Bonaventura Carlo, Egeo Gabriella, Pasini Elena, Cianci Vittoria, Ferlazzo Edoardo, Bianchi Amedeo, Coppola Giangennaro, Elia Maurizio, Mecarelli Oriano, Gobbi Giuseppe, Casellato Susanna, Marchini Marco, Binelli Simona, Freri Elena, Granata Tiziana, Posar Annio, Parmeggiani Antonia, Vigliano Piernanda, Boniver Clementina, Aguglia Umberto, Striano Salvatore, Tinuper Paolo, Giallonardo A Teresa, Michelucci Roberto, Nobile Car |
| Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling. Molecular genetics & genomic medicine 2016 Jul 4 (4): 447-56. Thomas Rhalena A, Ambalavanan Amirthagowri, Rouleau Guy A, Barker Philip |
| Anti-LGI1 encephalitis is associated with unique HLA subtypes. Annals of neurology 2016 Dec . Kim Tae-Joon, Lee Soon-Tae, Moon Jangsup, Sunwoo Jun-Sang, Byun Jung-Ick, Lim Jung-Ah, Shin Yong-Won, Jun Jin-Sun, Lee Han Sang, Lee Woo-Jin, Yang Ah Reaum, Choi Yunhee, Park Kyung-Il, Jung Keun-Hwa, Jung Ki-Young, Kim Manho, Lee Sang Kun, Chu K |
| 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 |
| 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 |
| Mesial temporal lobe epilepsy with hippocampal sclerosis is infrequently associated with neuronal autoantibodies. Epilepsia 2018 8 59 (9): e152-e156. Nóbrega-Jr Adaucto W, Gregory Christian P, Schlindwein-Zanini Rachel, Neves Fabricio de Souza, Wolf Peter, Walz Roger, Steindel Mario, Lin Kat |
| Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. American journal of human genetics 2019 Jul . , |
| 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 |
| 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 |
| Factors predicting uncontrolled seizures in epilepsy with auditory features. Seizure 2019 1 65 55-61. Zhang Lin, Zhu Xi, Zou Xiaoyi, Chen L |
| 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 |
| Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2024 7 . Hamide Betul Gerik-Celebi, ?pek Dokurel Çetin, Hilmi Bolat, Gul Unsel-Bol |
- Page last reviewed:Feb 1, 2024
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