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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 6, 2024. (Total: 232220Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Seizures and KCNT1[original query]
Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population.
CNS neuroscience & therapeutics 2013 Nov .
Qu J, Zhang Y, Yang ZQ, Mao XY, Zhou BT, Yin JY, He H, Li XP, Long HY, Lv N, Xu XJ, Xiao B, Zhang Y, Tang Q, Hu DL, Zhou HH, Liu ZQ
Mutations in KCNT1 cause a spectrum of focal epilepsies.
Epilepsia 2015 Sep 56 (9): e114-20.
Møller Rikke S, Heron Sarah E, Larsen Line H G, Lim Chiao Xin, Ricos Michael G, Bayly Marta A, van Kempen Marjan J A, Klinkenberg Sylvia, Andrews Ian, Kelley Kent, Ronen Gabriel M, Callen David, McMahon Jacinta M, Yendle Simone C, Carvill Gemma L, Mefford Heather C, Nabbout Rima, Poduri Annapurna, Striano Pasquale, Baglietto Maria G, Zara Federico, Smith Nicholas J, Pridmore Clair, Gardella Elena, Nikanorova Marina, Dahl Hans Atli, Gellert Pia, Scheffer Ingrid E, Gunning Boudewijn, Kragh-Olsen Bente, Dibbens Leanne
Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Neurology 2017 12 90 (1): e55-e66.
McTague Amy, Nair Umesh, Malhotra Sony, Meyer Esther, Trump Natalie, Gazina Elena V, Papandreou Apostolos, Ngoh Adeline, Ackermann Sally, Ambegaonkar Gautam, Appleton Richard, Desurkar Archana, Eltze Christin, Kneen Rachel, Kumar Ajith V, Lascelles Karine, Montgomery Tara, Ramesh Venkateswaran, Samanta Rajib, Scott Richard H, Tan Jeen, Whitehouse William, Poduri Annapurna, Scheffer Ingrid E, Chong W K Kling, Cross J Helen, Topf Maya, Petrou Steven, Kurian Manju
Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidine.
Neurology 2017 12 90 (1): e67-e72.
Mullen Saul A, Carney Patrick W, Roten Annie, Ching Michael, Lightfoot Paul A, Churilov Leonid, Nair Umesh, Li Melody, Berkovic Samuel F, Petrou Steven, Scheffer Ingrid
[Genetic and clinical analysis of children with early-onset epilepsy encephalopathy caused by KCNT1 gene mutation].
Zhonghua er ke za zhi = Chinese journal of pediatrics 2018 11 56 (11): 824-828.
Chen Y, Bao X H, Zhang Q P, Wang J P, Wen Y X, Yu S J, Zhao
Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies.
Genes, brain, and behavior 2018 Jan .
Zhou P, He N, Zhang J-W, Lin Z-J, Wang J, Yan L-M, Meng H, Tang B, Li B-M, Liu X-R, Shi Y-W, Zhai Q-X, Yi Y-H, Liao W
[Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event].
Zhonghua er ke za zhi = Chinese journal of pediatrics 2021 3 59 (4): 280-285.
Xiao T T, Yang L, Wu B B, Peng X M, Wang H J, Cheng G Q, Wang L S, Cao Y, Hu L Y, Zhou W
Analysis of clinical phenotypic and genotypic spectra in 36 children patients with Epilepsy of Infancy with Migrating Focal Seizures.
Scientific reports 2022 Jun 12 (1): 10187.
Yang Haiyan, Yang Xiaofan, Cai Fang, Gan Siyi, Yang Sai, Wu Liw
Next-generation sequencing testing in children with epilepsy reveals novel clinical, diagnostic and therapeutic implications.
Frontiers in genetics 2024 1 14 1300952.
Magdalena Krygier, Marta Pietruszka, Marta Zawadzka, Agnieszka Sawicka, Anna Lemska, Monika Limanówka, Jan ?urek, Weronika Tala?ka-Liczbik, Maria Mazurkiewicz-Be?dzi?s
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