Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Long QT dysrhythmias; Epilepsy and congenital long QT syndrome; Management of congenital long QT syndrome
مقالات ISI سندرم QT طولانی مدت مادرزادی (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.
A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome
Keywords: سندرم QT طولانی مدت مادرزادی; Drug-induced long QT syndrome; Congenital long QT syndrome; Torsades-de-Pointes; IKr blocking drugs; QT interval; Sudden death;
Non-sustained microvolt level T-wave alternans in congenital long QT syndrome types 1 and 2
Keywords: سندرم QT طولانی مدت مادرزادی; 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
Successful prenatal management of ventricular tachycardia and second-degree atrioventricular block in fetal long QT syndrome
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Ventricular arrhythmia; Prenatal management; Ventricular tachycardia/torsades de pointes; Fetal magnetocardiography;
Sevoflurane-associated torsade de pointes in a patient with congenital long QT syndrome genotype 2
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Genotype 2; Torsade de pointes; Volatile anesthetics
Predicting the Unpredictable: Drug-Induced QT Prolongation and Torsades de Pointes
Keywords: سندرم QT طولانی مدت مادرزادی; clinical decision support; pharmacogenomics; QT interval; sudden death; torsades de pointes; CDSS; clinical decision support systems; cLQTS; congenital long QT syndrome; diLQTS; drug-induced long QT syndrome; ECG; electrocardiogram; MC; mutation carrier;
Clinical presentation and course of long QT syndrome in Thai children
Keywords: سندرم QT طولانی مدت مادرزادی; Cardiac arrest; Cardiac arrhythmia; Cardiac conditions of childhood; Congenital long QT syndrome; Syncope; Thai children
Syncope and Sudden Cardiac Death in the Pediatric Athlete
Keywords: سندرم QT طولانی مدت مادرزادی; syncope; exercise related syncope; sudden cardiac death; hypertrophic cardiomyopathy; dilated cardiomyopathy; commotio cordis; congenital long QT syndrome; athlete's heart; pre-participation physical examination
Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2 : Higher Recurrence of Events Under Metoprolol
Keywords: سندرم QT طولانی مدت مادرزادی; breakthrough cardiac events; congenital long QT syndrome; metoprolol; nadolol; propranololACA, aborted cardiac arrest; BCE, breakthrough cardiac event; ECG, electrocardiogram; ICD, implantable cardioverter defibrillator; IQR, interquartile range; LCSD, le
Different subcellular populations of L-type Ca2+ channels exhibit unique regulation and functional roles in cardiomyocytes
Keywords: سندرم QT طولانی مدت مادرزادی; LTCC; L-type Ca2+ channel; EC; excitation-contraction; ICa,L; L-type Ca2+ current; SR; sarcoplasmic reticulum; T-tubules; transverse tubules; CICR; Ca2+-induced Ca2+ release; [Ca2+]i; free intracellular Ca2+ concentration; PKA; protein kinase A; Cav; ca
Perioperative management of hereditary arrhythmogenic syndromes
Keywords: سندرم QT طولانی مدت مادرزادی; anaesthesia; arrhythmogenic right ventricular dysplasia; Brugada syndrome; channelopathies; congenital long QT syndrome; congenital sick sinus syndrome; polymorphic catecholaminergic ventricular tachycardia;
Block of the hERG channel by bupivacaine: Electrophysiological and modeling insights towards stereochemical optimization
Keywords: سندرم QT طولانی مدت مادرزادی; Bupivacaine; Cardiotoxicity; Electrophysiology; hERG channel; Molecular docking; Stereoselectivity; AP; action potential; cLQTS; congenital long QT syndrome; diLQTS; drug-induced long QT syndrome; ECG; electrocardiogram; ES; extracellular solution; GB/SA;
Opioid maintenance patients with QTc prolongation: Congenital long QT syndrome mutation may be a contributing risk factor
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Genetic; Management; Methadone; QT prolongation
Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; hERG1; KCNH2; Takotsubo cardiomyopathy; Voltage-gated potassium channel; LQTS; long QT syndrome; PAS domain; Per-Arnt-Sim domain; WT; wild type;
In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: Compound effects of hERG pore region mutation and SCN5A N-terminus variant
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Atrioventricular block; Ventricular tachycardia; SCN5A; hERG; Mutation; Variant; Lidocaine
A successfully novel ICD implantation and medical treatment in a child with LQT syndrome and self-limiting ventricular fibrillation
Keywords: سندرم QT طولانی مدت مادرزادی; Congenital long QT syndrome; Flecainide; Beta-blockers; ICD