Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Seizures and GABRA1[original query] |
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Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures. Neuroscience letters 2005 Aug 383 (3): 220-4. Ito Minako, Ohmori Iori, Nakahori Tomoyuki, Ouchida Mamoru, Ohtsuka Yo |
Effects of SCN1A and GABA receptor genetic polymorphisms on carbamazepine tolerability and efficacy in Chinese patients with partial seizures: 2-year longitudinal clinical follow-up. CNS neuroscience & therapeutics 2012 Jul 18 (7): 566-72. Zhou Bo-Ting, Zhou Qiu-Hong, Yin Ji-Ye, Li Guo-Liang, Qu Jian, Xu Xiao-Jing, Liu Ding, Zhou Hong-Hao, Liu Zhao-Qi |
GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures. Pharmacogenetics and genomics 2013 Nov 23 (11): 605-10. Balan Shabeesh, Sathyan Sanish, Radha Saradalekshmi K, Joseph Vijai, Radhakrishnan Kurupath, Banerjee Moin |
Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. Neurology 2016 Aug . Johannesen Katrine, Marini Carla, Pfeffer Siona, Møller Rikke S, Dorn Thomas, Niturad Christina, Gardella Elena, Weber Yvonne, Søndergård Marianne, Hjalgrim Helle, Nikanorova Mariana, Becker Felicitas, Larsen Line H G, Dahl Hans A, Maier Oliver, Mei Davide, Biskup Saskia, Klein Karl M, Reif Philipp S, Rosenow Felix, Elias Abdallah F, Hudson Cindy, Helbig Katherine L, Schubert-Bast Susanne, Scordo Maria R, Craiu Dana, Djémié Tania, Hoffman-Zacharska Dorota, Caglayan Hande, Helbig Ingo, Serratosa Jose, Striano Pasquale, De Jonghe Peter, Weckhuysen Sarah, Suls Arvid, Muru Kai, Talvik Inga, Talvik Tiina, Muhle Hiltrud, Borggraefe Ingo, Rost Imma, Guerrini Renzo, Lerche Holger, Lemke Johannes R, Rubboli Guido, Maljevic Sneza |
Evaluating the Role of Genetic Variants on first-line antiepileptic drug response in North India: Significance of SCN1A and GABRA1 Gene Variants in Phenytoin Monotherapy and its Serum Drug Levels. CNS neuroscience & therapeutics 2016 09 22 (9): 740-57. Baghel Ruchi, Grover Sandeep, Kaur Harpreet, Jajodia Ajay, Rawat Chitra, Srivastava Ankit, Kushwaha Suman, Agarwal Rachna, Sharma Sangeeta, Kukreti Ritushr |
Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular syndromology 2016 Sep 7 (4): 210-219. Møller Rikke S, Larsen Line H G, Johannesen Katrine M, Talvik Inga, Talvik Tiina, Vaher Ulvi, Miranda Maria J, Farooq Muhammad, Nielsen Jens E K, Svendsen Lene Lavard, Kjelgaard Ditte B, Linnet Karen M, Hao Qin, Uldall Peter, Frangu Mimoza, Tommerup Niels, Baig Shahid M, Abdullah Uzma, Born Alfred P, Gellert Pia, Nikanorova Marina, Olofsson Kern, Jepsen Birgit, Marjanovic Dragan, Al-Zehhawi Lana I K, Peñalva Sofia J, Krag-Olsen Bente, Brusgaard Klaus, Hjalgrim Helle, Rubboli Guido, Pal Deb K, Dahl Hans |
Novel and de novo mutations in pediatric refractory epilepsy. Molecular brain 2018 9 11 (1): 48. Liu Jing, Tong Lili, Song Shuangshuang, Niu Yue, Li Jun, Wu Xiu, Zhang Jie, Zai Clement C, Luo Fang, Wu Jian, Li Haiyin, Wong Albert H C, Sun Ruopeng, Liu Fang, Li Baom |
Association of GABAA Receptor Gene with Epilepsy Syndromes. Journal of molecular neuroscience : MN 2018 May . Bhat Musadiq Ahmad, Guru Sameer Ahmad, Mir Rashid, Waza Ajaz Ahmad, Zuberi Mariyam, Sumi Mamta Pervin, Bodeliwala Shaam, Puri Vinod, Saxena Alpa |
Impact of GABA receptor gene variants (rs2279020 and rs211037) on the risk of predisposition to epilepsy: a case-control study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Feb . Amjad Maryam, Tabassum Atiya, Sher Khalid, Kumar Suneel, Zehra Sitwat, Fatima Sehri |
No association of GABRA1 rs2279020 and GABRA6 rs3219151 polymorphisms with risk of epilepsy and antiepileptic drug responsiveness in Asian and Arabic populations: Evidence from a meta-analysis with trial sequential analysis. Frontiers in neurology 2022 10 13 996631. Zhang Tiejun, Yang Yi, Sima Xiuti |
GABRA1-related disorders: from genetic to functional pathways. Annals of neurology 2023 8 . Elisa Musto, Vivian W Y Liao, Katrine M Johannesen, Christina D Fenger, Damien Lederer, Kavitha Kothur, Katrina Fisk, Bruce Bennetts, Pascal Vrielynck, Delphine Delaby, Berten Ceulemans, Sarah Weckhuysen, Peter Sparber, Arjan Bouman, Simone Ardern-Holmes, Christopher Troedson, Domenica I Battaglia, Himanshu Goel, Timothy Feyma, Somayeh Bakhtiari, Linda Tjoa, Martin Boxill, Nina Demina, Olga Shchagina, Elena Dadali, Michael Kruer, Gaetano Cantalupo, Ilaria Contaldo, Tilman Polster, Bertrand Isidor, Stefania M Bova, Walid Fazeli, Leen Wouters, Maria J Miranda, Francesca Darra, Elisa Pede, Diana Le Duc, Rami Abou Jamra, Sébastien Küry, Jacopo Proietti, Niamh McSweeney, Elly Brokamp, Peter Ian Andrews, Marie Gouray Garcia, Mary Chebib, Rikke S Møller, Philip K Ahring, Elena Gardel |
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