HuGE Literature Finder
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| Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients. BMC neurology 2021 Sep 21 (1): 367. Lin Chih-Hsiang, Ho Chen-Jui, Lu Yan-Ting, Tsai Meng-H |
| SCN1A and SCN1B gene polymorphisms and their association with plasma concentrations of carbamazepine and carbamazepine 10, 11 epoxide in Iranian epileptic patients. Iranian journal of basic medical sciences 2015 Dec 18 (12): 1215-20. Namazi Soha, Azarpira Negar, Javidnia Katayoon, Emami Mehrdad, Rahjoo Rahimeh, Berahmand Razieh, Borhani-Haghighi Afsh |
| Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy. Human genetics 2014 May 133 (5): 651-9. Baum Larry, Haerian Batoul Sadat, Ng Ho-Keung, Wong Virginia C N, Ng Ping Wing, Lui Colin H T, Sin Ngai Chuen, Zhang Chunbo, Tomlinson Brian, Wong Gary Wing-Kin, Tan Hui Jan, Raymond Azman Ali, Mohamed Zahurin, Kwan Patri |
| SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients. Scientific reports 2014 4 6470. Ricci Maria Teresa, Menegon Silvia, Vatrano Simona, Mandrile Giorgia, Cerrato Natascia, Carvalho Paula, De Marchi Mario, Gaita Fiorenzo, Giustetto Carla, Giachino Daniela Frances |
| Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy. Epilepsy research 2012 Dec 102 (3): 195-200. Wang Ji-wen, Shi Xiu-yu, Kurahashi Hirokazu, Hwang Su-Kyeong, Ishii Atsushi, Higurashi Norimichi, Kaneko Sunao, Hirose Shinichi, |
| Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+? Epilepsia 2009 Apr 50 (4): 953-6. Sijben Angelique E J, Sithinamsuwan Pasiri, Radhakrishnan Ashalata, Badawy Radwa A B, Dibbens Leanne, Mazarib Aziz, Lev Dorit, Lerman-Sagie Tally, Straussberg Rachel, Berkovic Samuel F, Scheffer Ingrid |
| Gene-to-gene interaction between sodium channel-related genes in determining the risk of antiepileptic drug resistance. Journal of Korean medical science 2009 Feb 24 (1): 62-8. Jang Sin-Young, Kim Myeong-Kyu, Lee Kee-Ra, Park Man-Seok, Kim Byeong-Chae, Cho Ki-Hyun, Lee Min-Cheol, Kim Yo-S |
| A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. Neurobiology of disease 2008 Dec 32 (3): 349-54. Ohmori Iori, Ouchida Mamoru, Miki Takafumi, Mimaki Nobuyoshi, Kiyonaka Shigeki, Nishiki Teiichi, Tomizawa Kazuhito, Mori Yasuo, Matsui Hide |
| Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children. Journal of biomedical science 2005 Oct 12 (5): 815-8. Haider M Z, Habeeb Y, Al-Nakkas E, Al-Anzi H, Zaki M, Al-Tawari A, Al-Bloushi |
| Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB). Epilepsia 2004 Feb 45 (2): 140-8. Fukuma Goryu, Oguni Hirokazu, Shirasaka Yukiyoshi, Watanabe Kazuyoshi, Miyajima Tasuku, Yasumoto Sawa, Ohfu Masaharu, Inoue Takahito, Watanachai Aruchalean, Kira Ryutaro, Matsuo Muneaki, Muranaka Hideki, Sofue Fumiko, Zhang Bo, Kaneko Sunao, Mitsudome Akihisa, Hirose Shinic |
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- Page last updated:May 11, 2022
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