Keywords: Sudden unexplained death; Channelopathies; Genetics; Molecular autopsy; Muerte súbita inexplicada; CanalopatÃas; Genética; Autopsia molecular;
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: Ion channels; Channelopathies; Neuron; Excitability; Neurologic diseases; Folding; Trafficking; Negative dominance;
Keywords: Channelopathies; Genetics; Infarction; Myocardium;
Keywords: Ventricular fibrillation; Brugada syndrome; Mitral valve prolapse; Sudden cardiac death; Channelopathies; Arrhythmogenic right ventricular dysplasia/cardiomyopathy;
Keywords: Channelopathies; Sudden cardiac death; Brugada syndrome
Keywords: Syncope; Children; Adolescents; Channelopathies; Tilt testSyncope; Enfants; Adolescents; Canalopathies; Tilt testCT, computed tomography; LOC, loss of consciousness; MRI, magnetic resonance imaging; NCS, neurocardiogenic syncope; PPS, psychogenic pseudosy
Keywords: Cardiomyopathies; Channelopathies; Marfan syndrome; Sudden cardiac death; MiocardiopatÃas; CanalopatÃas; SÃndrome de Marfan; Muerte súbita; HCM; hypertrophic cardiomyopathy; ICVD; inherited cardiovascular disease;
Keywords: Channelopathies; Dynamic causal modeling; Magnetoencephalography; Ion channel signaling; Biophysical models;
Keywords: ACMG; American College of Medical Genetics; BrS; Brugada syndrome; CPVT; catecholaminergic polymorphic ventricular tachycardia; ECG; electrocardiogram; ICD; implantable cardioverter-defibrillator; LQTS; long QT syndrome; VUS; variants of uncertain/unknown
Keywords: Channelopathies; Long QT syndrome; Short QT syndrome; Brugada syndrome; Catecholaminergic polymorphic ventricular tachycardia; Sudden cardiac death; ATS; Anderson-Tawil syndrome; AP-A; anthopleurin-A; APD; action potential duration; BrS; Brugada syndrom
Keywords: Channelopathies; Ion channel; Nondystrophic myotonia; Periodic paralysis; Congenital myasthenic syndrome;
Keywords: Sudden unexpected death in epilepsy; Seizures; Tonic-clonic; Epilepsy; Generalized; Nucleus of the solitary tract; Long QT syndrome; Apnea; Central; Arrhythmia; Cardiac; Channelopathies;
Keywords: Channelopathies; Inherited Arrhythmias
Keywords: Methadone; QT interval; Channelopathies; Repolarization reserve
Brugada Syndrome: A Primer for Nurse Practitioners
Keywords: Brugada syndrome; channelopathies; electrocardiogram; sudden cardiac death;
Muerte súbita cardiaca de origen arrÃtmico: valor del análisis genético post mortem
Keywords: Muerte súbita inexplicada; CanalopatÃas; Genética; Autopsia molecular; Sudden unexplained death; Channelopathies; Genetics; Molecular autopsy;
Seizure-like episodes and EEG abnormalities in patients with long QT syndrome
Keywords: SUDEP; LQTS; Channelopathies; Epilepsy; Syncope;
Brugada syndrome is associated with scar and endocardial involvement: Insights from high-density mapping with the Rhythmia⢠mapping system
Keywords: Brugada syndrome; Channelopathies; Epicardial ablation; Mapping systems; Rhythmiaâ¢; SÃndrome de Brugada; Canalopatias; Ablação epicárdica; Sistemas de mapeamento; Rhythmiaâ¢;
SÃndrome de Brugada
Keywords: CanalopatÃas; Muerte súbita; Channelopathies; Sudden death;
Clinical ObservationsInfantile Epileptic Encephalopathy Associated With SCN2A Mutation Responsive to Oral Mexiletine
Keywords: channelopathies; antiarrhythmic agents; lidocaine; epilepsy;
Case reportCongenital myopathy with “corona” fibres, selective muscle atrophy, and craniosynostosis associated with novel recessive mutations in SCN4A
Keywords: Congenital myopathy; SCN4A; Corona fibres; Channelopathies;
Cardiac transplantation in children and adolescents with long QT syndrome
Keywords: Cardiac arrest; Cardiac arrhythmias; Channelopathies; Child; Extracorporeal membrane oxygenation; Heart transplant; Infant; Long QT syndrome; Pediatrics;
Troubles congénitaux du rythme cardiaque chez l'enfant. Quelles recommandations pour l'anesthésie ?
Keywords: Anesthésie pédiatrique; Syndrome de Wolff-Parkinson-White; Canalopathies; Syndrome du QT long congénital; Tachycardie ventriculaire catécholergique; Syndrome de Brugada; Paediatric anaesthesia; Wolff-Parkinson-White Syndrome; Channelopathies; Long QT
Protocolo de actuación en las cardiopatÃas familiares: sÃntesis de recomendaciones y algoritmos de actuación
Keywords: MiocardiopatÃas; CanalopatÃas; SÃndrome de Marfan; Muerte súbita; Cardiomyopathies; Channelopathies; Marfan syndrome; Sudden cardiac death; CF; cardiopatÃa familiar; MCH; miocardiopatÃa hipertrófica;
CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
Keywords: Ataxia; Cerebellum; Migraine; ATP1A3 gene; Channelopathies; Episodic encephalopathy; Fever;
Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies
Keywords: ACC/AHA Scientific Statements; athletes; Brugada syndrome; cardiovascular abnormalities; channelopathies; heart rhythm disorders; long QT syndrome;
The multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiology
Keywords: Cardiac sodium channel; Channelopathies; Nav1.5; SCN5A; Sodium channel kinetics; Nav1.5 biology;
Genética de la muerte súbita inexplicada
Keywords: Muerte súbita inexplicada; Canalopatías; GenéticaSudden unexplained death; Channelopathies; Genetics
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings
Keywords: Early infantile epileptic encephalopathy; Suppression-burst; Genetic counseling; Channelopathies; Mosaic mutation
Altered and dynamic ion selectivity of K+ channels in cell development and excitability
Keywords: channelopathies; resting potential; cationic channels; ionic pore; dynamic ion selectivity; K2P channels; excitability; pH-sensitive; hypokalemia
ReviewMolecular mechanisms linking neuroinflammation and neurodegeneration in MS
Keywords: Multiple sclerosis; Neuroinflammation; Neurodegeneration; Mitochondrial dysfunction; Channelopathies;
Disease Caused by Mutations in NaV-β Subunit Genes
Keywords: Sodium channel β subunits; Sudden cardiac death; Epilepsy; Channelopathies; Long QT syndrome; Atrial fibrillation; Brugada syndrome;
Impact of Genetics on the Clinical Management of Channelopathies
Keywords: channelopathies; gene-specific management; genetic testing; heart rhythm disorder; sudden death; BrS; Brugada syndrome; CPVT; catecholaminergic polymorphic ventricular tachycardia; ECG; electrocardiogram; ICD; implantable cardioverter defibrillator; JLN;
What is new in Brugada syndrome?
Keywords: Brugada syndrome; Arrhythmia; Sudden cardiac death; ST-segment elevation; Channelopathies
Medicina personalizada: diagnóstico genético de cardiopatÃas/canalopatÃas hereditarias
Keywords: CMPi; células madre pluripotenciales inducidas; CPVT; taquicardia ventricular polimórfica catecolaminérgica; ECG; electrocardiograma; LQTS; sÃndrome de QT largo; MCH; miocardiopatÃa hipertrófica; SB; sÃndrome de Brugada; Genética; Canales iónicos
Structure, function and clinical relevance of the cardiac conduction system, including the atrioventricular ring and outflow tract tissues
Keywords: Cardiac conduction system; Atrioventricular ring tissue; Right ventricular outflow tract; Arrhythmias; Biopacemaking; Channelopathies
Paroxysmal neuromyotonia: A new sporadic channelopathy
Keywords: Neuromyotonia; Channelopathies; Acetazolamide;
Perioperative management of hereditary arrhythmogenic syndromes
Keywords: anaesthesia; arrhythmogenic right ventricular dysplasia; Brugada syndrome; channelopathies; congenital long QT syndrome; congenital sick sinus syndrome; polymorphic catecholaminergic ventricular tachycardia;
Coexisting vasospastic angina and undiagnosed Brugada Syndrome resulting in cardiac arrest
Keywords: Brugada; Coronary spasm; Channelopathies; Left main coronary
Long-Term Follow-Up of Patients With Short QT Syndrome
Keywords: arrhythmias; channelopathies; hydroquinidine; implantable cardioverter defibrillator; short-QT syndrome; sudden deathAF, atrial fibrillation; CA, cardiac arrest; ECG, electrocardiography; EPS, electrophysiological study; ERP, effective refractory period;
Inherited Cardiac Arrhythmia Syndrome: Role of Potassium Channels
Keywords: Potassium channels; Channelopathies; Sudden cardiac death; Genetics; Arrhythmias;
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
Keywords: Genetics; Cardiomyopathies; Channelopathies;
The genetics of epilepsy—The past, the present and future
Keywords: Epilepsy; Molecular genetics; Families; Channelopathies; Phenocopy; Next generation sequencing
Sudden cardiac death with normal heart: : molecular autopsy
Keywords: Autopsy; Channelopathies; Genetic screening; Normal heart; Sudden death
Inherited cardiac disease
Keywords: arrhythmogenic right ventricular dysplasia; cardiomyopathy; channelopathies; dilated cardiomyopathy; genetic; hypertrophic; mutation; sudden cardiac death;
Genetic Testing for Cardiac Arrhythmias: Ready for Prime Time?
Keywords: Genetics; Cardiac; Arrhythmias; Channelopathies; Multidisciplinary approach;
The year in arrhythmias-2009 Part II
Keywords: Sudden death; Ventricular tachycardia; Autonomic control; Pacemakers; Implantable defibrillators; Lead extraction; Ventricular fibrillation; Channelopathies; Inherited arrhythmogenic myopathies; Ablation; Cardiac resynchronization therapy; Dysautonomic sy
Brugada Syndrome 2010
Keywords: Brugada syndrome; Channelopathies; Inherited arrhythmias; Ventricular fibrillation; Sudden cardiac death; Implantable cardioverter-defibrillator;
Epileptogenic ion channel mutations: From bedside to bench and, hopefully, back again
Keywords: Epilepsy; Seizures; Excitability; Genetics; Ion currents; Channelopathies
Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A
Keywords: Sudden death; Sodium channel; Long QT syndrome; Channelopathies; Ventricular tachycardia