Keywords: سندرم QT طولانی; cardiomyocyte; cardiomyopathy; differentiation; long QT syndrome; pluripotent stem cellAPD, action potential duration; ARVD/C, arrhythmogenic right ventricular dysplasia/cardiomyopathy; CM, cardiomyocyte; CVD, cardiovascular disease; DCM, dilated cardiomy
مقالات ISI سندرم QT طولانی (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سندرم QT طولانی; ARVC; arrhythmogenic right ventricular cardiomyopathy; CASPER; Cardiac Arrest Survivors with Preserved Ejection Fraction Registry; CPVT; catecholaminergic polymorphic ventricular tachycardia; ECG; electrocardiogram/electrocardiographic; ERS; early repolar
Keywords: سندرم QT طولانی; Methadone; pain management; long QT syndrome; electrocardiography; analgesic-opioid/adverse effects; primary health care;
Keywords: سندرم QT طولانی; Sodium channel; SIDS; Stillbirth; IUFD; Long QT syndrome; Perinatal mortality; Genetics;
Keywords: سندرم QT طولانی; Induced pluripotent stem cells; Cardiac disease model; Two-photon initiated polymerization; Long QT syndrome; Cardiac contractility; Drug testing;
Keywords: سندرم QT طولانی; ADL; activity of daily living; ARVC; arrhythmogenic right ventricular cardiomyopathy; CI; confidence interval; CPVT; catecholaminergic polymorphic ventricular tachycardia; ECG; electrocardiogram/electrocardiography; HCM; hypertrophic cardiomyopathy; IQR;
Keywords: سندرم QT طولانی; Sudden unexpected death in epilepsy; Seizures; Tonic-clonic; Epilepsy; Generalized; Nucleus of the solitary tract; Long QT syndrome; Apnea; Central; Arrhythmia; Cardiac; Channelopathies;
Keywords: سندرم QT طولانی; Long QT syndrome; Borderline long QT; Medications; Preparticipation examination
Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes
Keywords: سندرم QT طولانی; Arrhythmia; Calmodulin; Long QT syndrome; Calcium channel;
Phenotypic Landscape and Risk Management in Long QT Syndrome
Keywords: سندرم QT طولانی; arrhythmia; beta-blockers; long QT syndrome;
Genotype-phenotype-guided medical and surgical intervention in long QT syndrome
Keywords: سندرم QT طولانی; Arrhythmia; Electrophysiology; Left cardiac sympathetic denervation; Long QT syndrome; Sudden cardiac death;
Wearable cardioverter defibrillators for patients with long QT syndrome
Keywords: سندرم QT طولانی; Long QT syndrome; LQTS; Sudden cardiac death; Syncope; Wearable cardioverter defibrillator;
A novel CACNA1C mutation identified in a patient with Timothy syndrome without syndactyly exerts both marked loss- and gain-of-function effects
Keywords: سندرم QT طولانی; Electrophysiology; Genetics; Long QT syndrome; L-type calcium channel; Timothy syndrome;
Non-sustained microvolt level T-wave alternans in congenital long QT syndrome types 1 and 2
Keywords: سندرم QT طولانی; DoR; dispersion of repolarization; LQTS; long QT syndrome; LQT1; long QT syndrome type 1; LQT2; long QT syndrome type 2; TdP; torsades de pointes; MTWA; microvolt T-wave alternans; NS-MTWA; non-sustained microvolt T-wave alternans; HR; heart rate; GNFC; g
Genotype and clinical characteristics of congenital long QT syndrome in Thailand
Keywords: سندرم QT طولانی; Long QT syndrome; Genetics; Mutation; Thailand; Children;
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Keywords: سندرم QT طولانی; Long QT syndrome; KCNH2; Mutation; Patch-clamp; Immunofluorescence;
Even pore-localizing missense variants at highly conserved sites in KCNQ1-encoded Kv7.1 channels may have wild-type function and not cause type 1 long QT syndrome: Do not rely solely on the genetic test company's interpretation
Keywords: سندرم QT طولانی; Arrhythmia; Cardiac arrest; Genetics; Long QT syndrome; Pediatrics;
Suppression of hERG K+ current and cardiac action potential prolongation by 4-hydroxynonenal via dual mechanisms
Keywords: سندرم QT طولانی; IKr; rapidly activating delayed rectifier potassium current in cardiomyocyte; IKs; slowly activating delayed rectifier potassium current in cardiomyocyte; ICa,L; , L-type calcium current in cardiomyocyte; IhERG; outward K+ current in hERG overexpressed co
A challenge for mutation specific risk stratification in long QT syndrome type 1
Keywords: سندرم QT طولانی; Long QT syndrome; KCNQ1; Mutation location; Sudden death;
Eleclazine exhibits enhanced selectivity for long QT syndrome type 3-associated late Na+ current
Keywords: سندرم QT طولانی; Sodium channel; Eleclazine; Ranolazine; Long QT syndrome; Brugada syndrome;
Microvolt T-wave alternans monitoring in a patient with levofloxacin-induced Torsade de Pointes
Keywords: سندرم QT طولانی; Drug-induced; Long QT syndrome; Torsade de Pointes; Microvolt T-wave alternans;
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome
Keywords: سندرم QT طولانی; genetic heart diseases; molecular autopsy; sudden infant death syndrome; whole exome sequencing; GHD; genetic heart disease; gnomAD; Genome Aggregation Database; LQTS; long QT syndrome; MAF; minor allele frequency; NSV; nonsynonymous variant; PCA; princip
The congenital long QT syndrome Type 3: An update
Keywords: سندرم QT طولانی; Long QT syndrome; Long QT syndrome-type-3; Torsade de Pointes; Electrocardiogram;
Drug-induced life-threatening arrhythmias and sudden cardiac death: A clinical perspective of long QT, short QT and Brugada syndromes
Keywords: سندرم QT طولانی; Sudden cardiac death; Long QT syndrome; Torsades de pointes; Short QT syndrome; Brugada syndrome; Pharmaceutical preparations; Morte súbita cardÃaca; SÃndrome do QT longo; Torsades de pointes; SÃndrome do QT curto; SÃndrome de Brugada; Preparações
Probing flecainide block of INa using human pluripotent stem cell-derived ventricular cardiomyocytes adapted to automated patch-clamping and 2D monolayers
Keywords: سندرم QT طولانی; AP; action potential; APD; action potential duration; EAD; early after-depolarization; EP; electrophysiology; ESCs; embryonic stem cells; FLE; flecainide; hESC; human embryonic stem cell; hPSC; human pluripotent stem cell; hPSC-CMs; human pluripotent stem
Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations
Keywords: سندرم QT طولانی; Early detection; Fetal heart rate; In utero bradycardia; Jervell and Lange-Nielsen syndrome; Long QT syndrome; Presymptomatic risk stratification;
Perioperative management of patients with congenital or acquired disorders of the QT interval
Keywords: سندرم QT طولانی; anaesthesia; long QT syndrome; perioperative care; torsades de pointes;
Unique ECG presentations and clinical management of a symptomatic LQT2 female carrying a novel de novo KCNH2 mutation
Keywords: سندرم QT طولانی; Long QT syndrome; Syncope; Cardiac arrest, torsade de pointes; Sudden cardiac death; KCNH2 mutation;
Risk of cardiac events in Long QT syndrome patients when taking antiseizure medications
Keywords: سندرم QT طولانی; ASM; antiseizure medication; GABA; gamma-aminobutyric acid; ECG; electrocardiogram; LQTS; Long QT syndrome; Na+Ch; Na+ channel; QTc; corrected QT; SCD; sudden cardiac death; SUDEP; sudden unexpected death in epilepsy;
Beyond the length and look of repolarization: Defining the non-QTc electrocardiographic profiles of patients with congenital long QT syndrome
Keywords: سندرم QT طولانی; Arrhythmia; Electrocardiography; Long QT syndrome; Sudden cardiac death;
The role of mexiletine in the management of long QT syndrome
Keywords: سندرم QT طولانی; Long QT syndrome; Late sodium currents; Rate-dependent QT prolongation mexiletine;
Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant
Keywords: سندرم QT طولانی; Arrhythmia; Genetics; Long QT syndrome; LQT5-Lite; Sudden death;
Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign
Keywords: سندرم QT طولانی; Arrhythmia; Genetics; Heart arrest; KCNQ1; Long QT syndrome; Pediatrics;
Abnormal Repolarization Duration During Everyday Emotional Arousal in Long QT Syndrome and Coronary Artery Disease
Keywords: سندرم QT طولانی; Coronary artery disease; Emotion; Long QT syndrome; QT interval; Sudden cardiac death; Ventricular repolarization;
Functional characterization of a novel hERG variant in a family with recurrent sudden infant death syndrome: Retracting a genetic diagnosis
Keywords: سندرم QT طولانی; Sudden infant death syndrome; Genotype-phenotype correlation; Long QT syndrome; hERG; Channel gating;
Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise
Keywords: سندرم QT طولانی; Genetic testing; Genetics; Long QT syndrome; Mutation; Variant of undetermined significance; Whole exome sequencing;
Complex aberrant splicing in the induced pluripotent stem cell-derived cardiomyocytes from a patient with long QT syndrome carrying KCNQ1-A344Aspl mutation
Keywords: سندرم QT طولانی; Aberrant splicing; IKs activator; Induced pluripotent stem cell; KCNQ1; Long QT syndrome;
Significance of T-wave inversion triggered by spontaneous atrial premature beats in patients with long QT syndrome
Keywords: سندرم QT طولانی; Atrial premature beat; Continuous 12-lead electrocardiography; Long QT syndrome; Microvolt T-wave alternans; Torsades de pointes; T-wave inversion;
Arrhythmias precede cardiomyopathy and remodeling of Ca2+ handling proteins in a novel model of long QT syndrome
Keywords: سندرم QT طولانی; Scn5a; Long QT syndrome; Arrhythmias; Intracellular Ca2+ homeostasis; Structural defects;
The genetic architecture of long QT syndrome: A critical reappraisal
Keywords: سندرم QT طولانی; Arrhythmia; Genetic testing; Genetic variation; Long QT syndrome; Sudden cardiac death; ABS; ankyrin-B syndrome; ACMG; American College of Medical Genetics and Genomics; aLQTS; acquired/drug-induced LQTS; AMP; Association for Molecular Pathology; Ca2+; ca
Cardiovascular Effects of Energy Drinks in Familial Long QT Syndrome: A Randomized Cross-Over Study
Keywords: سندرم QT طولانی; LQTS; long QT syndrome; QTc; corrected QT interval; ED; energy drink; CD; control drink; ECG; electrocardiogram; Long QT syndrome; energy drinks;
Atypical long QT syndrome phenotype in heterozygous/homozygous KCNQ1 Ala590Thr
Keywords: سندرم QT طولانی; Genotype-phenotype correlation; Heterozygous; Homozygous; Long QT syndrome; Protein trafficking;
Anesthesia for children with long QT syndrome: Challenges and solutions from pediatric studies
Keywords: سندرم QT طولانی; Prolonged QT interval; Long QT syndrome; Long QT syndrome and anesthesia; Anesthesia and pediatric arrhythmias; Anesthesia and genetic disorders in children;
Electrophysiological mechanisms of long and short QT syndromes
Keywords: سندرم QT طولانی; Cardiac arrhythmia; Repolarization; Long QT syndrome; Short QT syndrome; Wavelength;
Ten-year experience in atenolol use and exercise evaluation in children with genetically proven long QT syndrome
Keywords: سندرم QT طولانی; LQTS; Long QT syndrome; LQT1; Long QT syndrome type 1; LQT2; Long QT syndrome type 2; QTc; Corrected QT; min; Minutes; s; Seconds; ECG; Electrocardiogram; ICD; Implantable cardioverter-defibrillator; SFM; Screened family members; SD; Standard deviation; L
Divergent antiarrhythmic effects of resveratrol and piceatannol in a whole-heart model of long QT syndrome
Keywords: سندرم QT طولانی; Long QT syndrome; Sudden cardiac death; Resveratrol; Dispersion of repolarization;
Prevalence of Electrocardiographic Patterns Associated With Sudden Cardiac Death in the Spanish Population Aged 40 Years or Older. Results of the OFRECE Study
Keywords: سندرم QT طولانی; Sudden death; Epidemiology; Long QT syndrome; Tachyarrhythmias; Muerte súbita; EpidemiologÃa; SÃndrome de QT largo; Taquiarritmias; AF; atrial fibrillation; ECG; electrocardiogram; QTc; corrected QT; SCD; sudden cardiac death;
Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome
Keywords: سندرم QT طولانی; Holter; Individualized QT correction; QT-RR relation; QT rate dependence; Long QT syndrome; QTi;
Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene
Keywords: سندرم QT طولانی; Andersen-Tawil syndrome; Long QT syndrome; Arrhythmia; K897T polymorphism;
Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene
Keywords: سندرم QT طولانی; SCN5A; Long QT syndrome; Brugada syndrome; Promoter; Sudden death;