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cardiovascular (98) 98
index medicus (93) 93
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cardiology (36) 36
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arrhythmia (30) 30
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implants, artificial (19) 19
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pedigree (14) 14
brugada syndrome - diagnosis (13) 13
retrospective studies (13) 13
risk assessment (13) 13
sodium channels - genetics (13) 13
genes (12) 12
nav1.5 voltage-gated sodium channel (12) 12
brugada-syndrome (11) 11
defibrillators (11) 11
defibrillators, implantable (11) 11
prognosis (11) 11
risk (11) 11
st-segment elevation (11) 11
tachycardia (11) 11
arrhythmias (10) 10
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children (10) 10
disease (10) 10
follow-up studies (10) 10
genetic predisposition to disease (10) 10
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arrhythmias, cardiac - genetics (9) 9
care and treatment (9) 9
case-control studies (9) 9
death, sudden, cardiac - epidemiology (9) 9
dna mutational analysis (9) 9
heart conduction system - physiopathology (9) 9
implantable cardioverter-defibrillator (9) 9
muscle proteins - genetics (9) 9
prevalence (9) 9
atrial fibrillation (8) 8
bundle-branch block (8) 8
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ion channels (8) 8
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arrhythmogenic right ventricular dysplasia - genetics (7) 7
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death, sudden, cardiac - prevention & control (7) 7
electrophysiologic techniques, cardiac (7) 7
erg1 potassium channel (7) 7
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1. Full Text J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge
by Antzelevitch, Charles and Yan, Gan-Xin and Ackerman, Michael J and Borggrefe, Martin and Corrado, Domenico and Guo, Jihong and Gussak, Ihor and Hasdemir, Can and Horie, Minoru and Huikuri, Heikki and Ma, Changsheng and Morita, Hiroshi and Nam, Gi-Byoung and Sacher, Frederic and Shimizu, Wataru and Viskin, Sami and Wilde, Arthur A. M
Journal of arrhythmia, ISSN 1880-4276, 2016, Volume 32, Issue 5, pp. 315 - 339
Brugada Syndrome - mortality | Brugada Syndrome - diagnosis | Heart Rate | Predictive Value of Tests | Diagnosis, Differential | Prognosis | Risk Assessment | Brugada Syndrome - physiopathology | Humans | Risk Factors | Death, Sudden, Cardiac - prevention & control | Death, Sudden, Cardiac - etiology | Consensus | Action Potentials | Heart Conduction System - physiopathology | Electrocardiography | Electrophysiologic Techniques, Cardiac | Brugada Syndrome - therapy
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2. Full Text Risk Stratification in Brugada Syndrome
by Wilde, Arthur A.M., MD, PhD and Postema, Pieter G., MD, PhD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 67, Issue 12, pp. 1441 - 1443
Cardiovascular | Internal Medicine | Medical colleges
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3. Full Text Challenging the unifying pathophysiological concept of J-wave syndromes
by Wilde, Arthur A.M., MD, PhD, FHRS
Heart Rhythm, ISSN 1547-5271, 2016, Volume 13, Issue 8, pp. 1729 - 1730
Cardiovascular | Ventricular arrhythmias | Early repolarization | J-wave syndromes | Brugada syndrome | Electrocardiogram | CARDIAC & CARDIOVASCULAR SYSTEMS | Early repoLarization | IDIOPATHIC VENTRICULAR-FIBRILLATION | Medical colleges | Index Medicus
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4. Full Text A new ECG section in Heart Rhythm by Josephson and Wellens
by Buxton, Alfred E., MD and Wilde, Arthur A.M., MD, PhD and Chen, Peng-Sheng, MD
Heart Rhythm, ISSN 1547-5271, 2014, Volume 11, Issue 12, pp. 2328 - 2328
Cardiovascular
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5. Full Text The “Accordion Sign,” a New Tune in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Magnetic Resonance Imaging?
by Groenink, Maarten, MD, PhD and Wilde, Arthur A.M., MD, PhD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2009, Volume 53, Issue 15, pp. 1300 - 1301
Cardiovascular | Internal Medicine | diagnosis | magnetic resonance imaging | genetics | cardiomyopathy | arrhythmia
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6. Full Text An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
by Kapplinger, Jamie D., BA and Tester, David J., BS and Alders, Marielle, PhD and Benito, Begoña, MD and Berthet, Myriam, BA and Brugada, Josep, MD, PhD and Brugada, Pedro, MD, PhD and Fressart, Véronique, MD and Guerchicoff, Alejandra, PhD and Harris-Kerr, Carole, PhD and Kamakura, Shiro, MD, PhD and Kyndt, Florence, PhD and Koopmann, Tamara T., PhD and Miyamoto, Yoshihiro, MD and Pfeiffer, Ryan, BS and Pollevick, Guido D., PhD and Probst, Vincent, MD, PhD and Zumhagen, Sven, MD and Vatta, Matteo, PhD and Towbin, Jeffrey A., MD and Shimizu, Wataru, MD, PhD and Schulze-Bahr, Eric, MD and Antzelevitch, Charles, PhD and Salisbury, Benjamin A., PhD and Guicheney, Pascale, PhD and Wilde, Arthur A.M., MD, PhD and Brugada, Ramon, MD, PhD and Schott, Jean-Jacques, PhD and Ackerman, Michael J., MD, PhD
Heart Rhythm, ISSN 1547-5271, 2010, Volume 7, Issue 1, pp. 33 - 46
Background Brugada syndrome (BrS) is a common heritable channelopathy. Mutations in the SCN5A -encoded sodium channel (BrS1) culminate in the most common... 
Cardiovascular | Ion channels | Sodium channel | Genetic testing | Brugada syndrome | Sudden death | CARDIAC & CARDIOVASCULAR SYSTEMS | VARIANTS | GENOMIC ORGANIZATION | LONG-QT SYNDROME | PREVALENCE | BUNDLE-BRANCH BLOCK | SPLICING MUTATIONS | NA+ CHANNEL | DISEASE | SCN5A | ST-SEGMENT ELEVATION | Brugada Syndrome - genetics | Multivariate Analysis | Genetic Testing | Death, Sudden, Cardiac - epidemiology | Humans | Middle Aged | Child, Preschool | Databases, Genetic | Infant | Male | Mutation, Missense | Case-Control Studies | Young Adult | Aged, 80 and over | Adult | Female | Retrospective Studies | Child | NAV1.5 Voltage-Gated Sodium Channel | Global Health | Risk Factors | Exons - genetics | Genotype | Muscle Proteins - genetics | Internationality | Adolescent | Brugada Syndrome - epidemiology | Aged | Sodium Channels - genetics | Polymerase chain reaction | Heart failure | Proteins | Medical colleges | Molecular genetics | Analysis | Physiological aspects | Children | Cardiology | Population genetics | Genetic screening | Diseases | Index Medicus
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7. Full Text Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome
by Lahrouchi, Najim, MD and Raju, Hariharan, MBChB, PhD and Lodder, Elisabeth M., PhD and Papatheodorou, Efstathios, MD and Ware, James S., PhD and Papadakis, Michael, MBBS, MD and Tadros, Rafik, MD, PhD and Cole, Della, BSc and Skinner, Jonathan R., MBChB, MD and Crawford, Jackie and Love, Donald R., PhD and Pua, Chee J., PhD and Soh, Bee Y., PhD and Bhalshankar, Jaydutt D., PhD and Govind, Risha, MSc and Tfelt-Hansen, Jacob, MD, DMSc and Winkel, Bo G., MD, PhD and van der Werf, Christian, MD, PhD and Wijeyeratne, Yanushi D., BMBS and Mellor, Greg, MBChB, MD and Till, Jan, MD and Cohen, Marta C., MD, DMJ (Pathol) and Tome-Esteban, Maria, MD, PhD and Sharma, Sanjay, MBChB, MD and Wilde, Arthur A.M., MD, PhD and Cook, Stuart A., MD, PhD and Bezzina, Connie R., PhD and Sheppard, Mary N., MB, BCh, BAO, MD and Behr, Elijah R., MBBS, MD
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 17, pp. 2134 - 2145
Abstract Background Sudden arrhythmic death syndrome (SADS) describes a sudden death with negative autopsy and toxicological analysis. Cardiac genetic disease... 
Cardiovascular | Internal Medicine | cardiomyopathy | next-generation sequencing | channelopathy | molecular autopsy | unexplained sudden death | CARDIAC & CARDIOVASCULAR SYSTEMS | VARIANTS | ABNORMALITIES | RISK | YOUNG | DISEASE | CARDIAC DEATH | ASSOCIATION | Young Adult | Genetic Testing | Humans | Adolescent | Adult | Female | Male | Death, Sudden, Cardiac - etiology | Child | Medical colleges | Medical research | Genetic disorders | Analysis | Medicine, Experimental | Research institutes | Cardiology | Genetic screening | Medical genetics | Heart | Panels | Connectin | Cardiomyopathy | Disorders | Association analysis | Ryanodine receptors | Cardiovascular disease | Family medical history | Assaying | Risk factors | Incidence | Alignment | Autopsy | Classification | Inbreeding | Genetics | Libraries | Diagnosis | Bioinformatics | Probes | Deoxyribonucleic acid--DNA | Evaluation | Pathogens | Echocardiography | Baits | Abnormalities | Mortality | Nucleic acids | Pathogenicity | Studies | Hospitals | Sodium | Fibrosis | Death | Cardiovascular diseases | Circulation | Computer assisted instruction--CAI | Cardiac arrhythmia | Animal models | Electric contacts | Exons | Genes | Genomes | Agglomeration | Guidelines | Defibrillators | Syncope | Quality | Children | Heart diseases | Hum | Autopsies | Nucleotide sequence | Health risks | Data processing | Coronary artery disease | Magnetic resonance imaging | Resonance | Ventricle | Gene mapping | Index Medicus | Abridged Index Medicus | VUS, variant of unknown significance | MAF, minor allele frequency | SCD, sudden cardiac death | ACMG, American College of Medical Genetics | LQTS, long QT syndrome | BrS, Brugada syndrome | ACM, arrhythmogenic cardiomyopathy | CPVT, catecholaminergic polymorphic ventricular tachycardia | SADS, sudden arrhythmic death syndrome | Original Investigation
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8. Full Text Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
by van der Werf, Christian, MD and Kannankeril, Prince J., MD, MSCI and Sacher, Frederic, MD and Krahn, Andrew D., MD and Viskin, Sami, MD and Leenhardt, Antoine, MD and Shimizu, Wataru, MD, PhD and Sumitomo, Naokata, MD and Fish, Frank A., MD and Bhuiyan, Zahurul A., MD, PhD and Willems, Albert R., MD, PhD and van der Veen, Maurits J., MD, PhD and Watanabe, Hiroshi, MD, PhD and Laborderie, Julien, MD and Haïssaguerre, Michel, MD and Knollmann, Björn C., MD, PhD and Wilde, Arthur A.M., MD, PhD
Journal of the American College of Cardiology, ISSN 0735-1097, 2011, Volume 57, Issue 22, pp. 2244 - 2254
Objectives This study evaluated the efficacy and safety of flecainide in addition to conventional drug therapy in patients with catecholaminergic polymorphic... 
Cardiovascular | Internal Medicine | ventricular arrhythmia | antiarrhythmia agents | catecholaminergic polymorphic ventricular tachycardia | CARDIAC & CARDIOVASCULAR SYSTEMS | SUDDEN-DEATH | FOLLOW-UP | RECEPTOR CA2+ RELEASE | DEPOLARIZATION | THRESHOLD | CHANNEL | FAMILIES | RYR2 MUTATIONS | CASQ2 | CARDIAC SYMPATHETIC DENERVATION | Arrhythmias, Cardiac - prevention & control | Flecainide - administration & dosage | Tachycardia, Ventricular - drug therapy | Anti-Arrhythmia Agents - pharmacology | Humans | Middle Aged | Male | Flecainide - pharmacology | Anti-Arrhythmia Agents - therapeutic use | Anti-Arrhythmia Agents - administration & dosage | Dose-Response Relationship, Drug | Young Adult | Exercise Test | Defibrillators, Implantable | Adolescent | Adult | Female | Aged | Retrospective Studies | Child | Flecainide - therapeutic use | Heart failure | Medical colleges | Care and treatment | Implants, Artificial | Prosthesis | Cardiac patients | Ventricular tachycardia | Cardiology | Flecainide | Medical genetics | Children | Health aspects | Cardiovascular agents | Cardiac arrhythmia | Heart attacks | Exercise | Defibrillators | Blood | Index Medicus | Abridged Index Medicus
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9. Full Text Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise
by Kapplinger, Jamie D., BA and Landstrom, Andrew P., BS and Salisbury, Benjamin A., PhD and Callis, Thomas E., PhD and Pollevick, Guido D., PhD and Tester, David J., BS and Cox, Moniek G.P.J., MD and Bhuiyan, Zahir, MD, PhD and Bikker, Hennie, PhD and Wiesfeld, Ans C.P., MD, PhD and Hauer, Richard N.W., MD and van Tintelen, J. Peter, MD, PhD and Jongbloed, Jan D.H., PhD and Calkins, Hugh, MD and Judge, Daniel P., MD and Wilde, Arthur A.M., MD, PhD and Ackerman, Michael J., MD, PhD
Journal of the American College of Cardiology, ISSN 0735-1097, 2011, Volume 57, Issue 23, pp. 2317 - 2327
Objectives The aims of this study were to determine the spectrum and prevalence of “background genetic noise” in the arrhythmogenic right ventricular... 
Cardiovascular | Internal Medicine | mutation | arrhythmogenic right ventricular cardiomyopathy | diagnosis | arrhythmogenic right ventricular dysplasia | genetic testing | CARDIAC & CARDIOVASCULAR SYSTEMS | VARIANTS | PLAKOPHILIN-2 | IMPACT | DISEASE | DESMOGLEIN-2 | TASK-FORCE CRITERIA | DYSPLASIA/CARDIOMYOPATHY | Arrhythmogenic Right Ventricular Dysplasia - genetics | Genetic Predisposition to Disease | Genetic Testing | Prevalence | DNA Mutational Analysis | Humans | Middle Aged | Adult | Arrhythmogenic Right Ventricular Dysplasia - epidemiology | Case-Control Studies | Medical colleges | Dysplasia | Cardiomyopathy | DNA | Genetic research | Genetic aspects | Children | Cardiology | Heart diseases | Genetic screening | Diseases | Therapeutics | Medical genetics | Homeopathy | Materia medica and therapeutics | Proteins | Studies | Ethnicity | Genes | Mutation | Genetic testing | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus | Arrhythmogenic right ventricular cardiomyopathy
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10. Full Text Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals
by Goldenberg, Ilan, MD and Horr, Samuel, MA and Moss, Arthur J., MD and Lopes, Coeli M., PhD and Barsheshet, Alon, MD and McNitt, Scott, MS and Zareba, Wojciech, MD, PhD and Andrews, Mark L., BBA and Robinson, Jennifer L., MS and Locati, Emanuela H., MD and Ackerman, Michael J., MD, PhD and Benhorin, Jesaia, MD and Kaufman, Elizabeth S., MD and Napolitano, Carlo, MD and Platonov, Pyotr G., MD, PhD and Priori, Silvia G., MD, PhD and Qi, Ming, MD and Schwartz, Peter J., MD and Shimizu, Wataru, MD, PhD and Towbin, Jeffrey A., MD and Vincent, G. Michael, MD and Wilde, Arthur A.M., MD, PhD and Zhang, Li, MD and Kardiologi and Cardiology and Lund University and Lunds universitet
Journal of the American College of Cardiology, ISSN 0735-1097, 2011, Volume 57, Issue 1, pp. 51 - 59
Objectives This study was designed to assess the clinical course and to identify risk factors for life-threatening events in patients with long-QT syndrome... 
Cardiovascular | Internal Medicine | corrected QT interval | long-QT syndrome | sudden cardiac death | ARREST | CARDIAC & CARDIOVASCULAR SYSTEMS | GENE | GENDER | DEATH | CLINICAL-COURSE | Long QT Syndrome - complications | Prognosis | Global Health | Death, Sudden, Cardiac - epidemiology | Humans | Middle Aged | Risk Factors | Heart Arrest - epidemiology | Genotype | Male | Survival Rate | Death, Sudden, Cardiac - etiology | Long QT Syndrome - physiopathology | Young Adult | Adolescent | Electrocardiography | Heart Arrest - etiology | Long QT Syndrome - genetics | Adult | Female | Aged | Child | Medical colleges | Care and treatment | Cardiology | Cardiac patients | Electrocardiogram | Research institutes | Cardiac arrhythmia | Heart attacks | Mutation | Drug therapy | Index Medicus | Abridged Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
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11. Full Text Rationale and design of the PRAETORIAN trial: A Prospective, RAndomizEd comparison of subcuTaneOus and tRansvenous ImplANtable cardioverter-defibrillator therapy
by Olde Nordkamp, Louise R.A., MD and Knops, Reinoud E., MD and Bardy, Gust H., MD and Blaauw, Yuri, MD, PhD and Boersma, Lucas V.A., MD, PhD and Bos, Johannes S., MD, PhD and Delnoy, Peter Paul H.M., MD, PhD and van Dessel, Pascal F.H.M., MD, PhD and Driessen, Antoine H.G., MD and de Groot, Joris R., MD, PhD and Herrman, Jean Paul R., MD, PhD and Jordaens, Luc J.L.M., MD, PhD and Kooiman, Kirsten M., CCDS and Maass, Alexander H., MD, PhD and Meine, Mathias, MD, PhD and Mizusawa, Yuka, MD and Molhoek, Sander G., MD, PhD and van Opstal, Jurjen, MD, PhD and Tijssen, Jan G.P., PhD and Wilde, Arthur A.M., MD, PhD and PRAETORIAN Investigators
American Heart Journal, ISSN 0002-8703, 2012, Volume 163, Issue 5, pp. 753 - 760.e2
Background Implantable cardioverter-defibrillators (ICDs) are widely used to prevent fatal outcomes associated with life-threatening arrhythmic episodes in a... 
Cardiovascular | CARDIAC & CARDIOVASCULAR SYSTEMS | TOLERABILITY | COLLABORATION | AMERICAN-COLLEGE | PREVENTION | ASSOCIATION TASK-FORCE | BURST | GUIDELINES WRITING COMMITTEE | RAPID VENTRICULAR-TACHYCARDIA | TERMINATION | SHOCKS | Tachycardia, Ventricular - therapy | Prospective Studies | Double-Blind Method | Follow-Up Studies | Risk Assessment | Humans | Death, Sudden, Cardiac - prevention & control | Male | Survival Rate | Treatment Outcome | Equipment Design | Cross-Over Studies | Tachycardia, Ventricular - mortality | Heart Arrest - mortality | Heart Conduction System - physiopathology | Defibrillators, Implantable | Tachycardia, Ventricular - diagnosis | Electrocardiography | Female | Equipment Safety | Heart Arrest - therapy | Clinical trials | Comparative analysis | Implants, Artificial | Prosthesis | Analysis | Cardiac arrhythmia | Skin | Defibrillators | Mortality | Quality of life | Index Medicus | Abridged Index Medicus
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12. Full Text Genotype-Phenotype Aspects of Type 2 Long QT Syndrome
by Shimizu, Wataru, MD, PhD and Moss, Arthur J., MD and Wilde, Arthur A.M., MD, PhD and Towbin, Jeffrey A., MD and Ackerman, Michael J., MD, PhD and January, Craig T., MD, PhD and Tester, David J., BS and Zareba, Wojciech, MD, PhD and Robinson, Jennifer L., MS and Qi, Ming, PhD and Vincent, G. Michael, MD and Kaufman, Elizabeth S., MD and Hofman, Nynke, MSc and Noda, Takashi, MD, PhD and Kamakura, Shiro, MD, PhD and Miyamoto, Yoshihiro, MD, PhD and Shah, Samit, BA and Amin, Vinit, MA and Goldenberg, Ilan, MD and Andrews, Mark L., BBA and McNitt, Scott, MS
Journal of the American College of Cardiology, ISSN 0735-1097, 2009, Volume 54, Issue 22, pp. 2052 - 2062
Objectives The purpose of this study was to investigate the effect of location, coding type, and topology of KCNH2(hERG) mutations on clinical phenotype in... 
Cardiovascular | Internal Medicine | syncope | genetics | long QT syndrome | arrhythmia | electrocardiography | LQT2 | LOCATION | CARDIAC & CARDIOVASCULAR SYSTEMS | EVENTS | MECHANISM | CARDIAC-ARRHYTHMIA | RISK | HERG | GENE | MUTATIONS | POTASSIUM CHANNEL | Humans | Proportional Hazards Models | Models, Molecular | Genotype | Male | Codon, Nonsense | Mutation, Missense | ERG1 Potassium Channel | Ether-A-Go-Go Potassium Channels - genetics | Protein Structure, Secondary - genetics | Young Adult | Phenotype | Membrane Potentials | Adolescent | Long QT Syndrome - genetics | Adult | Female | Retrospective Studies | Child | Long QT syndrome | Medical colleges | Genetic aspects | Molecular genetics | Cardiology | Medical genetics | Proteins | Confidence intervals | Genotype & phenotype | Heart attacks | Population | Mutation | Index Medicus | Abridged Index Medicus | long-QT syndrome
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13. Full Text Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2
by Chockalingam, Priya, MBBS, PhD and Crotti, Lia, MD, PhD and Girardengo, Giulia, MD and Johnson, Jonathan N., MD and Harris, Katy M., MS, RN and van der Heijden, Jeroen F., MD, PhD and Hauer, Richard N.W., MD, PhD and Beckmann, Britt M., MD and Spazzolini, Carla, DVM, MS and Rordorf, Roberto, MD and Rydberg, Annika, MD, PhD and Clur, Sally-Ann B., MBBCh, MSc (Med), PhD and Fischer, Markus, MD and van den Heuvel, Freek, MD, PhD and Kääb, Stefan, MD, PhD and Blom, Nico A., MD, PhD and Ackerman, Michael J., MD, PhD and Schwartz, Peter J., MD and Wilde, Arthur A.M., MD, PhD
Journal of the American College of Cardiology, ISSN 0735-1097, 2012, Volume 60, Issue 20, pp. 2092 - 2099
Objectives The purpose of this study was to compare the efficacy of beta-blockers in congenital long QT syndrome (LQTS). Background Beta-blockers are the... 
Cardiovascular | Internal Medicine | nadolol | congenital long QT syndrome | metoprolol | breakthrough cardiac events | propranolol | CARDIAC & CARDIOVASCULAR SYSTEMS | EVENTS | EFFICACY | GENOTYPE | FAILURES | PHENOTYPE | RISK | THERAPY | Heart failure | Medical colleges | Genetic disorders | Prosthesis | Nadolol | Diseases | Heart beat | Implants, Artificial | Electrocardiogram | Long QT syndrome | Electrocardiography | Children | Cardiology | Therapeutics | Homeopathy | Materia medica and therapeutics | Confidence intervals | Variables | Genotype & phenotype | Consciousness | Mutation | Drug therapy | Females | Age
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14. Full Text A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence
by Marsman, Roos F., MD and Barc, Julien, PhD and Beekman, Leander, BSc and Alders, Marielle, PhD and Dooijes, Dennis, PhD and van den Wijngaard, Arthur, PhD and Ratbi, Ilham, MD and Sefiani, Abdelaziz, MD, PhD and Bhuiyan, Zahurul A., MD, PhD and Wilde, Arthur A.M., MD, PhD and Bezzina, Connie R., PhD
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 63, Issue 3, pp. 259 - 266
Objectives This study aimed to identify the genetic defect in a family with idiopathic ventricular fibrillation (IVF) manifesting in childhood and adolescence.... 
Cardiovascular | Internal Medicine | idiopathic ventricular fibrillation | ventricular arrhythmia | exome sequencing | genetics | calmodulin | CARDIAC & CARDIOVASCULAR SYSTEMS | LONG-QT SYNDROME | CONSTRAINT | PENETRANCE | CARDIAC-ARREST | CHANNEL | ALIGNMENT | YEAST CALMODULIN | DISEASE | BINDING | EXPRESSION | Calmodulin - genetics | Genetic Predisposition to Disease | Ventricular Fibrillation - metabolism | Humans | Male | DNA - genetics | Monomeric Clathrin Assembly Proteins - genetics | DNA Mutational Analysis | Pedigree | Adolescent | Electrocardiography | Ventricular Fibrillation - genetics | Ventricular Fibrillation - physiopathology | Female | Mutation | Child | Sects | Medical colleges | Abnormalities | Genetic research | Genetic aspects | Muscle contraction | Calmodulin | Cardiac arrhythmia | Heart attacks | Genes | Index Medicus | Abridged Index Medicus
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