Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutationKUI HONG; JINZHU HU; JIANHUA YU et al.European journal of human genetics. 2012, Vol 20, Num 11, pp 1189-1192, issn 1018-4813, 4 p.Article

Des anomalies génétiques augmentent le risque de mort subite du nourrissonCASSELYN, Marina.Biofutur (Puteaux). 2006, Num 265, pp 17-17, issn 0294-3506Article

Regional variations in action potential alternans in isolated murine Scn5a^+/- hearts during dynamic pacingMATTHEWS, G. D. K; MARTIN, C. A; GRACE, A. A et al.Acta physiologica (Print). 2010, Vol 200, Num 2, pp 129-146, issn 1748-1708, 18 p.Article

Cardiomyocytes Obtained From Induced Pluripotent Stem Cells With Long-QT Syndrome 3 Recapitulate Typical Disease-Specific Features In VitroMALAN, Daniela; FRIEDRICHS, Stephanie; FLEISCHMANN, Bernd K et al.Circulation research. 2011, Vol 109, Num 8, pp 841-847, issn 0009-7330, 7 p.Article

Sodium Channel (Dys)Function and Cardiac ArrhythmiasREMME, Carol Ann; BEZZINA, Connie R.Cardiovascular therapeutics (Print). 2010, Vol 28, Num 5, pp 287-294, issn 1755-5914, 8 p.Article

Cardiac sodium channel Na_v1.5 and its associated proteinsABRIEL, H.Archives des maladies du coeur et des vaisseaux. 2007, Vol 100, Num 9, pp 787-793, issn 0003-9683, 7 p.Article

A novel SCN5A mutation associated with the linker between III and IV domains of Na_v1.5 in a neonate with fatal long QT syndromeYAMAMURA, Kenichiro; MUNEUCHI, Jun; HARA, Toshiro et al.International journal of cardiology. 2010, Vol 145, Num 1, pp 61-64, issn 0167-5273, 4 p.Article

Mutation-specific pharmacology of the long QT syndromeKASS, R. S; MOSS, A. J.Handbook of experimental pharmacology. 2006, Vol 171, pp 287-304, issn 0171-2004, 18 p.Article

A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardiaCHANG, Chien-Chih; ACHARFI, Said; WU, Mei-Hwan et al.Cardiovascular research. 2004, Vol 64, Num 2, pp 268-278, issn 0008-6363, 11 p.Article

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndromeVATTA, Matteo; DUMAINE, Robert; HUA LI et al.Human molecular genetics (Print). 2002, Vol 11, Num 3, pp 337-345, issn 0964-6906Article

Novel sodium channel SCN5A mutations in Brugada syndrome patients from GreeceKOTTA, Christina-Maria; ANASTASAKIS, Aris; GATZOULIS, Konstantinos et al.International journal of cardiology. 2010, Vol 145, Num 1, pp 45-48, issn 0167-5273, 4 p.Article

Absence of Pathognomonic or Inflammatory Patterns in Cardiac Biopsies From Patients With Brugada SyndromeZUMHAGEN, Sven; SPIEKER, Tilmann; ROLINCK, Julia et al.Circulation. Arrhythmia and electrophysiology. 2009, Vol 2, Num 1, pp 16-23, issn 1941-3149, 8 p.Article

A novel SCN5A mutation, F1344S, identified in a patient with brugada syndrome and fever-induced ventricular fibrillationKELLER, Dagmar I; HAI HUANG; JUAN ZHAO et al.Cardiovascular research. 2006, Vol 70, Num 3, pp 521-529, issn 0008-6363, 9 p.Article

Modeling type 3 long QT syndrome with cardiomyocytes derived from patient-specific induced pluripotent stem cellsDONGRUI MA; HEMING WEI; COOK, Stuart A et al.International journal of cardiology. 2013, Vol 168, Num 6, pp 5277-5286, issn 0167-5273, 10 p.Article

Biology of cardiac sodium channel Na_v1.5 expressionROOK, Martin B; EVERS, Melvin M; VOS, Marc A et al.Cardiovascular research. 2012, Vol 93, Num 1, pp 12-23, issn 0008-6363, 12 p.Article

A Brugada syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterizationMARANGONI, Stefano; DI RESTA, Chiara; BENEDETTI, Sara et al.Cardiovascular research. 2011, Vol 91, Num 4, pp 606-616, issn 0008-6363, 11 p.Article

Cardiac Na+ channels as therapeutic targets for antiarrhythmic agentsGLAASER, I. W; CLANCY, C. E.Handbook of experimental pharmacology. 2006, Vol 171, pp 99-121, issn 0171-2004, 23 p.Article

Molecular basis of isolated cardiac conduction diseaseVISWANATHAN, P. C; BALSER, J. R.Handbook of experimental pharmacology. 2006, Vol 171, pp 331-347, issn 0171-2004, 17 p.Article

A novel 5' splice site mutation of SCN5A associated with Brugada syndrome resulting in multiple cryptic transcriptsSHIMADA, Toshio; OHKUBO, Kimie; ABE, Keisuke et al.International journal of cardiology. 2012, Vol 158, Num 3, pp 441-443, issn 0167-5273, 3 p.Article

Magnetic resonance investigations in Brugada syndrome reveal unexpectedly high rate of structural abnormalitiesCATALANO, Oronzo; ANTONACI, Serena; MONTEFORTE, Nicola et al.European heart journal. 2009, Vol 30, Num 18, pp 2241-2248, issn 0195-668X, 8 p.Article

Sodium channel mutation in irritable bowel syndrome : evidence for an ion channelopathySAITO, Yuri A; STREGE, Peter R; TESTER, David J et al.American journal of physiology. Gastrointestinal and liver physiology. 2009, Vol 59, Num 2, issn 0193-1857, G211-G218Article

A paradoxical effect of lidocaine for the N406 S mutation of SCN5A associated with Brugada syndromeITOH, Hideki; TSUJI, Keiko; HORIE, Minoru et al.International journal of cardiology. 2007, Vol 121, Num 3, pp 239-248, issn 0167-5273, 10 p.Article

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutationPARISI, Pasquale; OLIVA, Antonio; ZARA, Federico et al.Epilepsy research. 2013, Vol 105, Num 3, pp 415-418, issn 0920-1211, 4 p.Article

Blocking Scn10a Channels in Heart Reduces Late Sodium Current and Is AntiarrhythmicTAO YANG; ATACK, Thomas C; MYERS STROUD, Dina et al.Circulation research. 2012, Vol 111, Num 3, pp 322-332, issn 0009-7330, 11 p.Article

Molecular pharmacology of voltage-gated sodium channel expression in metastatic disease: Clinical potential of neonatal Nav1.5 in breast cancerONKAL, Rustem; DJAMGOZ, Mustafa B. A.European journal of pharmacology. 2009, Vol 625, Num 1-3, pp 206-219, issn 0014-2999, 14 p.Article