Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Epilepsy and KCNJ10[original query] |
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| Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility. Epilepsy research 2004 Feb 58 (2-3): 175-83. Buono R J, Lohoff F W, Sander T, Sperling M R, O'Connor M J, Dlugos D J, Ryan S G, Golden G T, Zhao H, Scattergood T M, Berrettini W H, Ferraro T |
| No association between common variations in the human alpha 2 subunit gene (ATP1A2) of the sodium-potassium-transporting ATPase and idiopathic generalized epilepsy. Neuroscience letters 0 382 (1-2): 33-8. Lohoff Falk W, Ferraro Thomas N, Sander Thomas, Zhao Hongyu, Dahl John P, Berrettini Wade H, Buono Russell |
| Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy research 2005 Feb 63 (2-3): 113-8. Lenzen K P, Heils A, Lorenz S, Hempelmann A, Höfels S, Lohoff F W, Schmitz B, Sander |
| Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy. Epilepsy research 2010 Jan 88 (1): 55-64. Heuser Kjell, Nagelhus Erlend A, Taubøll Erik, Indahl Ulf, Berg Paul R, Lien Sigbjørn, Nakken Sigve, Gjerstad Leif, Ottersen Ole Pett |
| Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. The Journal of physiology 2011 Apr 589 (Pt 7): 1681-9. Thompson Dorothy A, Feather Sally, Stanescu Horia C, Freudenthal Bernard, Zdebik Anselm A, Warth Richard, Ognjanovic Milos, Hulton Sally A, Wassmer Evangeline, van't Hoff William, Russell-Eggitt Isabelle, Dobbie Angus, Sheridan Eamonn, Kleta Robert, Bockenhauer Detl |
| Targeted next generation sequencing as a diagnostic tool in epileptic disorders. Epilepsia 2012 Aug 53 (8): 1387-98. Lemke Johannes R, Riesch Erik, Scheurenbrand Tim, Schubach Max, Wilhelm Christian, Steiner Isabelle, Hansen Jörg, Courage Carolina, Gallati Sabina, Bürki Sarah, Strozzi Susi, Simonetti Barbara Goeggel, Grunt Sebastian, Steinlin Maja, Alber Michael, Wolff Markus, Klopstock Thomas, Prott Eva C, Lorenz Rüdiger, Spaich Christiane, Rona Sabine, Lakshminarasimhan Maya, Kröll Judith, Dorn Thomas, Krämer Günter, Synofzik Matthis, Becker Felicitas, Weber Yvonne G, Lerche Holger, Böhm Detlef, Biskup Sask |
| Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts. BMC medical genetics 2013 14 85. Landa Priya, Differ Ann-Marie, Rajput Kaukab, Jenkins Lucy, Bitner-Glindzicz Mar |
| Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsies. PloS one 2015 10 (4): e0124896. Guo Yong, Yan Kui Po, Qu Qiang, Qu Jian, Chen Zi Gui, Song Tao, Luo Xiang-Ying, Sun Zhong-Yi, Bi Chang-Long, Liu Jin-Fa |
| Effects of AQP4 and KCNJ10 Gene Polymorphisms on Drug Resistance and Seizure Susceptibility in Chinese Han Patients with Focal Epilepsy. Neuropsychiatric disease and treatment 2020 16 119-129. Zhu Haoyue, Zhang Mengqi, Fu Yujiao, Long Hongyu, Xiao Wenbiao, Feng Li, Xiao Bo, Zhou L |
| Association of KCNJ10 variants and the susceptibility to clinical epilepsy. Clinical neurology and neurosurgery 2020 Oct 106340. Jiang Chuan, Li Lianping, Wu Mingxin, Hao Maolin, Feng Jian |
| Coexistence of temporal lobe epilepsy and idiopathic generalized epilepsy. Epilepsy & behavior : E&B 2023 12 151 109602. Ali A Asadi-Pooya, Mahdi Malekpour, Ehsan Taherifard, Arashk Mallahzadeh, Mohsen Farjoud Kouhanja |
- Page last reviewed:Feb 1, 2024
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