HuGE Literature Finder
Records 1-25
|
Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong.
Frontiers in physiology 2020 11 574590. Tse Gary, Lee Sharen, Liu Tong, Yuen Ho Chuen, Wong Ian Chi Kei, Mak Chloe, Mok Ngai Shing, Wong Wing T |
|
Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Cardiology 2019 Nov 1-8. Wang Feng, Liu Yang, Liao Hongtao, Xue Yumei, Zhan Xianzhang, Fang Xianhong, Liang Yuanhong, Wei Wei, Rao Fang, Zhang Qianhuan, Deng Hai, Lin Yubi, Liu Fangzhou, Lin Weidong, Zhang Bin, Wu Shul |
|
A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
PloS one 2017 12 (1): e0170193. Jabbari Reza, Glinge Charlotte, Jabbari Javad, Risgaard Bjarke, Winkel Bo Gregers, Terkelsen Christian Juhl, Tilsted Hans-Henrik, Jensen Lisette Okkels, Hougaard Mikkel, Haunsø Stig, Engstrøm Thomas, Albert Christine M, Tfelt-Hansen Jac |
|
Prognostic significance of fever-induced Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2016 Mar . Mizusawa Yuka, Morita Hiroshi, Adler Arnon, Havakuk Ofer, Thollet Aurélie, Maury Philippe, Wang Dao W, Hong Kui, Gandjbakhch Estelle, Sacher Frédéric, Hu Dan, Amin Ahmad S, Lahrouchi Najim, Tan Hanno L, Antzelevitch Charles, Probst Vincent, Viskin Sami, Wilde Arthur A |
|
Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current.
Circulation. Arrhythmia and electrophysiology 2016 Jan 9 (1): . Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Toshishige Masaaki, Tokuyama Takehito, Matsumura Hiroya, Kawazoe Hiroshi, Tomomori Shunsuke, Sairaku Akinori, Watanabe Yoshikazu, Ikenaga Hiroki, Motoda Chikaaki, Suenari Kazuyoshi, Hayashida Yasufumi, Miki Daiki, Oda Nozomu, Kishimoto Shinji, Oda Noboru, Yoshida Yukihiko, Tashiro Satoshi, Chayama Kazuaki, Kihara Yasu |
|
Genetics of Brugada syndrome.
Journal of human genetics 2015 Jul . Watanabe Hiroshi, Minamino Toh |
|
Purkinje-related ventricular fibrillation associated with a homozygous H558R polymorphism in the sodium channel SCN5A gene.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Jun . Reithmann Christopher, Beckmann Britt-Maria, Kääb Stef |
|
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Human molecular genetics 2015 May 24 (10): 2757-63. Le Scouarnec Solena, Karakachoff Matilde, Gourraud Jean-Baptiste, Lindenbaum Pierre, Bonnaud Stéphanie, Portero Vincent, Duboscq-Bidot Laëtitia, Daumy Xavier, Simonet Floriane, Teusan Raluca, Baron Estelle, Violleau Jade, Persyn Elodie, Bellanger Lise, Barc Julien, Chatel Stéphanie, Martins Raphaël, Mabo Philippe, Sacher Frédéric, Haïssaguerre Michel, Kyndt Florence, Schmitt Sébastien, Bézieau Stéphane, Le Marec Hervé, Dina Christian, Schott Jean-Jacques, Probst Vincent, Redon Richa |
|
Novel SCN10A variants associated with Brugada syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Apr . Fukuyama Megumi, Ohno Seiko, Makiyama Takeru, Horie Mino |
|
Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
International heart journal 2015 56 (4): 450-3. Chang Ya-Sian, Yang Yi-Wen, Lin Yen-Nien, Lin Kuo-Hung, Chang Kuan-Cheng, Chang Jan-Gow |
|
SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction.
Molecular medicine reports 2014 Oct 10 (4): 2039-44. Boehringer Tim, Bugert Peter, Borggrefe Martin, Elmas El |
|
L-type calcium channel mutations in Japanese patients with inherited arrhythmias.
Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1799-806. Fukuyama Megumi, Ohno Seiko, Wang Qi, Kimura Hiromi, Makiyama Takeru, Itoh Hideki, Ito Makoto, Horie Mino |
|
Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease.
Pacing and clinical electrophysiology : PACE 2011 Jun 34 (6): 742-9. Novotny Tomas, Kadlecova Jitka, Raudenska Martina, Bittnerova Alexandra, Andrsova Irena, Florianova Alena, Vasku Anna, Neugebauer Petr, Kozak Milan, Sepsi Milan, Krivan Lubomir, Gaillyova Renata, Spinar Jindri |
|
SCN5A mutation is associated with early and frequent recurrence of ventricular fibrillation in patients with Brugada syndrome.
Circulation journal : official journal of the Japanese Circulation Society 2010 Nov 74 (12): 2572-8. Nishii Nobuhiro, Ogawa Masahiro, Morita Hiroshi, Nakamura Kazufumi, Banba Kimikazu, Miura Daiji, Kumagai Naoko, Matsunaga Akira, Kawamura Hiroshi, Urakawa Shigemi, Miyaji Kohei, Nagai Masahiro, Satoh Katsumasa, Nakagawa Koji, Tanaka Masamichi, Hiramatsu Shigeki, Tada Takeshi, Murakami Masato, Nagase Satoshi, Kohno Kunihisa, Kusano Kengo Fukushima, Saku Keijiro, Ohe Tohru, Ito Hiros |
|
The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction.
Journal of cardiovascular electrophysiology 2010 Nov 21 (11): 1260-5. Elmas Elif, Bugert Peter, Popp Tatjana, Lang Siegfried, Weiss Christel, Behnes Michael, Borggrefe Martin, Kälsch Thorst |
|
Atrial electrophysiological and structural remodeling in high-risk patients with Brugada syndrome: assessment with electrophysiology and echocardiography.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 7 (2): 218-24. Toh Norihisa, Morita Hiroshi, Nagase Satoshi, Taniguchi Manabu, Miura Daiji, Nishii Nobuhiro, Nakamura Kazufumi, Ohe Tohru, Kusano Kengo F, Ito Hiros |
|
Differential effects of cardiac sodium channel mutations on initiation of ventricular arrhythmias in patients with Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2009 Apr 6 (4): 4. Morita H, Nagase S, Miura D, Miura A, Hiramatsu S, Tada T, Murakami M, Nishii N, Nakamura K, Morita ST, Oka T, Kusano KF, Ohe T |
|
Atrial fibrillation in patients with Brugada syndrome relationships of gene mutation, electrophysiology, and clinical backgrounds.
Journal of the American College of Cardiology 2008 Mar 51 (12): 1169-75. Kusano Kengo F, Taniyama Makiko, Nakamura Kazufumi, Miura Daiji, Banba Kimikazu, Nagase Satoshi, Morita Hiroshi, Nishii Nobuhiro, Watanabe Atsuyuki, Tada Takeshi, Murakami Masato, Miyaji Kohei, Hiramatsu Shigeki, Nakagawa Koji, Tanaka Masamichi, Miura Aya, Kimura Hideo, Fuke Soichiro, Sumita Wakako, Sakuragi Satoru, Urakawa Shigemi, Iwasaki Jun, Ohe Toh |
|
Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.
Circulation 2006 Jan 113 (3): 338-44. Bezzina Connie R, Shimizu Wataru, Yang Ping, Koopmann Tamara T, Tanck Michael W T, Miyamoto Yoshihiro, Kamakura Shiro, Roden Dan M, Wilde Arthur A |
|
Double SCN5A mutation underlying asymptomatic Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2005 Mar 2 (3): 285-92. Yokoi Hisataka, Makita Naomasa, Sasaki Koji, Takagi Yasuhiro, Okumura Yasuo, Nishino Tetsuo, Makiyama Takeru, Kitabatake Akira, Horie Minoru, Watanabe Ichiro, Tsutsui Hiroyu |
|
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms.
Journal of human genetics 2005 50 (9): 490-6. Lai Ling-Ping, Su Yi-Ning, Hsieh Fon-Jou, Chiang Fu-Tien, Juang Jyh-Ming, Liu Yen-Bin, Ho Yi-Lwun, Chen Wen-Jone, Yeh San-Jou, Wang Chun-Chieh, Ko Yu-Lin, Wu Tsu-Juey, Ueng Kwo-Chang, Lei Meng-Huan, Tsao Hsuan-Ming, Chen Shih-Ann, Lin Tin-Kwang, Wu Mei-Hwan, Lo Huey-Ming, Huang Shoei K Stephen, Lin Jiunn-L |
|
Single nucleotide polymorphisms of the SCN5A gene in Han Chinese and their relation with Brugada syndrome.
Chinese medical journal 2004 May 117 (5): 652-6. Chen Jun-zhu, Xie Xu-dong, Wang Xing-xiang, Tao Ming, Shang Yun-peng, Guo Xiao-ga |
|
[Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].
Sheng li xue bao : [Acta physiologica Sinica] 2004 Feb 56 (1): 36-40. Xie Xu-Dong, Wang Xing-Xiang, Chen Jun-Zhu, Tao Ming, Shang Yun-Peng, Guo Xiao-Gang, Zheng Liang-Ro |
|
Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome.
Journal of human genetics 2004 49 (10): 573-8. Shin Dong-Jik, Jang Yangsoo, Park Hyun-Young, Lee Jong Eun, Yang Keumjin, Kim Eunmin, Bae Yoonjung, Kim Jongmin, Kim Jeongki, Kim Sung Soon, Lee Moon Hyoung, Chahine Mohamed, Yoon Sungjoo K |
|
Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.
Human mutation 2003 Jun 21 (6): 651-2. Schulze-Bahr Eric, Eckardt Lars, Breithardt Günter, Seidl Karlheinz, Wichter Thomas, Wolpert Christian, Borggrefe Martin, Haverkamp Wilhe |
- Page last reviewed:Oct 1, 2020
- Page last updated:Sep 16, 2021
- Content source: