about
A calcium sensor in the sodium channel modulates cardiac excitabilityExpanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic featuresGenetic variation in SCN10A influences cardiac conductionA connexin40 mutation associated with a malignant variant of progressive familial heart block type ISodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansMultifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathySpectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testFlecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansDrugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)Navigating the mini-maze: systematic review of the first results and progress of minimally-invasive surgery in the treatment of atrial fibrillationArrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up studyFunctional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathyArrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a familyThe RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading framOverlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insDLeft cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardiaGenome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarctionCoxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaPlakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathyGenome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesGenetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationCongenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Clinical utility gene card for: long-QT syndrome (types 1-13).Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data.Proposed diagnostic criteria for the Brugada syndrome: consensus report.A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.Exercise related syncope, when it's not the heart.Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome.Syncope during exercise, documented with continuous blood pressure monitoring during ergometer testing.Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?Clinical aspects and prognosis of Brugada syndrome in children.Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.Vasovagal syncope or ventricular fibrillation. Your diagnosis better be accurate.Genetic aspects of vasovagal syncope: a systematic review of current evidence.Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?Value of history-taking in syncope patients: in whom to suspect long QT syndrome?Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome.Symptoms and signs of syncope: a review of the link between physiology and clinical clues.SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
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name
Arthur A M Wilde
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type
label
Arthur A M Wilde
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prefLabel
Arthur A M Wilde
@en