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Journal of Cardiovascular Electrophysiology, ISSN 1045-3873, 12/2019, Volume 30, Issue 12, pp. 2716 - 2723
Background A diagnosis of silent paroxysmal atrial fibrillation (AF) is highly challenging due to its asymptomatic and intermittent nature. The goal of the... 
silent paroxysmal atrial fibrillation | asymptomaticity | inducibility | atrioventricular conductivity | atrial ectopy | Heart rate | Radio frequency | Cardiac arrhythmia | Conduction | Stroke | Fibrillation | Refractory period | Medical instruments | Electrocardiography | Ablation | Catheters
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A12399 - A12399
IntroductionUrinary liver-type fatty acid-binding protein (L-FABP) is known as a potential biomarker for acute kidney injury. Its predictive value for... 
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A12225 - A12225
IntroductionAtrial fibrillation (AF) has a genetic basis, and environmental factors alter the actual AF pathogenesis. Perhaps, the identification of... 
Journal Article
PLOS ONE, ISSN 1932-6203, 03/2019, Volume 14, Issue 3, p. e0213208
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2018, Volume 13, Issue 9, p. e0203281
Introduction The single nucleotide polymorphism (SNP) rs2106261 in the transcription factor gene ZFHX3 (16q22), a major regulator of inflammation, has been... 
NEUTROPHIL/LYMPHOCYTE RATIO | METAANALYSIS | EXPERT CONSENSUS STATEMENT | MULTIDISCIPLINARY SCIENCES | CATHETER ABLATION | SURGICAL ABLATION | END-POINTS | FOLLOW-UP | PATIENT-MANAGEMENT | RESEARCH TRIAL DESIGN | PROCEDURAL TECHNIQUES | Recurrence | Genetic Predisposition to Disease | Gene Frequency | Humans | Middle Aged | Catheter Ablation | Male | Genetic Markers | Atrial Fibrillation - genetics | Atrial Fibrillation - surgery | Case-Control Studies | Homeodomain Proteins - genetics | Alleles | Inflammation - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Pulmonary Veins - surgery | Retrospective Studies | Prevention | Transcription factors | Atrial fibrillation | Physiological aspects | Development and progression | Genetic aspects | Inflammation | Research | Genetic polymorphisms | Health sciences | Cardiac arrhythmia | Biomedical research | C-reactive protein | Platelet-activating factor | Interleukin | Systematic review | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Interleukin 6 | Proteins | Genotype & phenotype | Signal transduction | Fibrillation | Audio frequencies | Gastroenterology | Cardiology | Chromosome 16 | University graduates | Multivariable control | Neutrophils | Metabolism | Gene expression | Patients | Ablation | Catheters | Medicine | Hospitals | Gene frequency | Polymorphism | Veins & arteries
Journal Article
Clinical Chemistry and Laboratory Medicine (CCLM), ISSN 1434-6621, 05/2018, Volume 56, Issue 6, pp. 147 - 149
N-terminal pro-brain natriuretic peptide (NT-pro BNP) is a reliable diagnostic marker of heart failure. It is widely recognized that its circulating levels are... 
diagnostic performance | left atrial pressure | persistent atrial fibrillation | NT-pro BNP | HEART-FAILURE | MEDICAL LABORATORY TECHNOLOGY | ASSOCIATION | Heart atrium | Physiological aspects | Brain natriuretic peptide | Diagnosis | Atrial fibrillation | Brain | Cardiac arrhythmia | Diagnostic systems | Fibrillation | Medical diagnosis
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, p. e103993
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 14565 - 6
Genome-wide association studies have reported a strong association of the single nucleotide polymorphism (SNP) rs6817105 (T > C) on chromosome 4q25 with atrial... 
FIBRILLATION | PREDISPOSITION | MULTIDISCIPLINARY SCIENCES | COMMON | LOCI | PITX2 | CONTRIBUTES | EXPRESSION | Phenotypes | Fibrillation | Sinuses | Gene frequency | Alleles | Electrocardiography | miRNA | Single-nucleotide polymorphism | Genomes | Chromosome 4 | Gene polymorphism
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A14395 - A14395
Risk stratification of Brugada syndrome (BrS) remains controversial and the majority of BrS patients have no genetic explanation. In a recent genome-wide... 
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A14731 - A14731
BackgroundThe AF related SNPs have been reported to be associated with the outcomes after AF ablation, but it remains controversial. We investigated the... 
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A14591 - A14591
ObjectivesThe common SCN5A polymorphism, rs1805124 (c.1673A>G, H558R), has been reported to improve the sodium channel activity in mutated channels and as a... 
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A13920 - A13920
IntroductionGenome-wide association studies (GWAS) have identified several single nucleotide polymorphisms (SNPs) associated with atrial fibrillation (AF). The... 
Journal Article
Thrombosis Research, ISSN 0049-3848, 11/2019, Volume 183, pp. 119 - 123
Atrial fibrillation (AF) ablation with minimally interrupted direct oral anticoagulants (DOACs) predominates, possibly raising concern about their remaining... 
Residual activity | Atrial fibrillation ablation | Direct oral anticoagulants | Temporary interruption | DABIGATRAN | WARFARIN | RIVAROXABAN | ABLATION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | BLEEDING COMPLICATIONS
Journal Article
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A12854 - A12854
IntroductionTelomeres are repetitive DNA sequences located at end of chromosomes and become shortened with age as a result of repeated somatic cell division.... 
Journal Article
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