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Journal of the American College of Cardiology, ISSN 0735-1097, 03/2018, Volume 71, Issue 11, pp. 1215 - 1216
In this issue of the Journal, Papadakis et al. (1) report a unique study in families with sudden arrhythmic death syndrome (SADS). Papadakis et al. (1) studied... 
sudden arrhythmic death syndrome | ion channelopathy | cardiomyopathy | ajmaline provocation testing | BRUGADA-SYNDROME | CARDIAC & CARDIOVASCULAR SYSTEMS | AJMALINE | LEADS | Autopsy | Death, Sudden, Cardiac | Humans | Heart | Cardiac arrhythmia | Mortality | Long QT syndrome | Electrocardiography | Medical diagnosis | Patients
Journal Article
Muscle & Nerve, ISSN 0148-639X, 04/2018, Volume 57, Issue 4, pp. 522 - 530
ABSTRACT Periodic paralyses (PPs) are rare neuromuscular disorders caused by mutations in skeletal muscle sodium, calcium, and potassium channel genes. PPs... 
treatment | periodic paralyses | review | acetazolamide | Andersen‐Tawil syndrome | channelopathies | dichlorphenamide | Andersen-Tawil syndrome | ACETAZOLAMIDE TREATMENT | EXERCISE TEST | FLECAINIDE | ANDERSEN-TAWIL-SYNDROME | SKELETAL-MUSCLE CHANNELOPATHIES | CHANNEL GENE SCN4A | WEAKNESS | KCNJ2 MUTATIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | VENTRICULAR-ARRHYTHMIAS | CARBONIC-ANHYDRASE INHIBITORS | Behavior Therapy | Humans | Andersen Syndrome - diagnosis | Paralysis, Hyperkalemic Periodic - therapy | Hypokalemic Periodic Paralysis - diagnosis | Anti-Arrhythmia Agents - therapeutic use | Paralyses, Familial Periodic - therapy | Andersen Syndrome - therapy | Paralyses, Familial Periodic - diagnosis | Paralysis, Hyperkalemic Periodic - diagnosis | Potassium - therapeutic use | Diuretics - therapeutic use | Hypokalemic Periodic Paralysis - therapy | Acetazolamide - therapeutic use | Hydrochlorothiazide - therapeutic use | Carbonic Anhydrase Inhibitors - therapeutic use | Diuretics, Potassium Sparing - therapeutic use | Care and treatment | Gene mutations | Therapeutics | Muscles | Diuretics | Paralysis | Diagnosis | Genetic screening | Homeopathy | Materia medica and therapeutics | Calcium | Heredity | Skeletal muscle | Sodium | Carbonic anhydrase | Mutation | Potassium | Neuromuscular system | Invited Reviews | Invited Review
Journal Article
Revista Española de Cardiología (English Edition), ISSN 1885-5857, 03/2016, Volume 69, Issue 3, pp. 300 - 309
The term inherited cardiovascular disease encompasses a group of cardiovascular diseases (cardiomyopathies, channelopathies, certain aortic diseases, and other... 
Channelopathies | Muerte súbita | Canalopatías | Síndrome de Marfan | Miocardiopatías | Cardiomyopathies | Sudden cardiac death | Marfan syndrome | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | MANAGEMENT | POSITION STATEMENT | GUIDELINES | EUROPEAN-SOCIETY | HYPERTROPHIC CARDIOMYOPATHY | EXPERT CONSENSUS STATEMENT | ESC | CARDIOLOGY WORKING GROUP | Brugada Syndrome - genetics | Long QT Syndrome - complications | Brugada Syndrome - diagnosis | Loeys-Dietz Syndrome - complications | Cardiomyopathy, Hypertrophic, Familial - genetics | Channelopathies - complications | Humans | Cardiovascular Diseases - therapy | Death, Sudden, Cardiac - prevention & control | Brugada Syndrome - complications | Death, Sudden, Cardiac - etiology | Cardiovascular Diseases - genetics | Marfan Syndrome - therapy | Cardiomyopathy, Hypertrophic, Familial - diagnosis | Channelopathies - diagnosis | Cardiomyopathy, Hypertrophic, Familial - complications | Cardiovascular Diseases - complications | Long QT Syndrome - diagnosis | Tachycardia, Ventricular - genetics | Cardiomyopathy, Dilated - diagnosis | Marfan Syndrome - complications | Arrhythmias, Cardiac - genetics | Cardiovascular Diseases - diagnosis | Cardiomyopathy, Dilated - genetics | Tachycardia, Ventricular - therapy | Genetic Predisposition to Disease | Tachycardia, Ventricular - complications | Arrhythmias, Cardiac - therapy | Cardiomyopathy, Dilated - complications | Loeys-Dietz Syndrome - diagnosis | Long QT Syndrome - therapy | Marfan Syndrome - genetics | Channelopathies - therapy | Loeys-Dietz Syndrome - therapy | Channelopathies - genetics | Algorithms | Cardiomyopathy, Hypertrophic, Familial - therapy | Tachycardia, Ventricular - diagnosis | Marfan Syndrome - diagnosis | Long QT Syndrome - genetics | Arrhythmias, Cardiac - complications | Arrhythmias, Cardiac - diagnosis | Loeys-Dietz Syndrome - genetics | Brugada Syndrome - therapy | Cardiomyopathy, Dilated - therapy | Practice Guidelines as Topic
Journal Article
Circulation, ISSN 0009-7322, 11/2007, Volume 116, Issue 20, pp. 2325 - 2345
Journal Article
Heart Rhythm, ISSN 1547-5271, 08/2018, Volume 15, Issue 8, pp. 1261 - 1267
Journal Article
Spanish Journal of Cardiology (Revista Española de Cardiología, English Edition), ISSN 1885-5857, 2017, Volume 70, Issue 10, pp. 808 - 816
Abstract Introduction and objectives Nonischemic sudden cardiac death (SCD) is predominantly caused by cardiomyopathies and channelopathies. There are many... 
Cardiovascular | Internal Medicine | Muerte súbita cardiaca | Arritmias | Estudio genético | Miocardiopatías | Fibrilación ventricular | Cardiomyopathies | Genetic testing | Sudden cardiac death | Arrhythmias | Ventricular fibrillation | Brugada Syndrome - genetics | Long QT Syndrome - complications | Brugada Syndrome - diagnosis | Genetic Testing | Channelopathies - complications | Humans | Middle Aged | Male | Brugada Syndrome - complications | Cardiomyopathy, Hypertrophic - complications | Death, Sudden, Cardiac - etiology | Arrhythmogenic Right Ventricular Dysplasia - diagnosis | Arrhythmogenic Right Ventricular Dysplasia - genetics | Young Adult | Cardiomyopathies - genetics | Channelopathies - diagnosis | Heart Defects, Congenital - genetics | Exercise Test | Long QT Syndrome - diagnosis | Cardiomyopathies - diagnosis | Electrocardiography | Tachycardia, Ventricular - genetics | Adult | Cardiomyopathy, Dilated - diagnosis | Female | Retrospective Studies | Child | Arrhythmias, Cardiac - genetics | Cardiomyopathy, Dilated - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | Tachycardia, Ventricular - complications | Cardiomyopathy, Dilated - complications | Cardiomyopathy, Hypertrophic - diagnosis | Sequence Analysis, DNA | Arrhythmogenic Right Ventricular Dysplasia - complications | Channelopathies - genetics | Phenotype | Heart Defects, Congenital - complications | Tachycardia, Ventricular - diagnosis | Adolescent | Long QT Syndrome - genetics | Cardiomyopathies - complications | Family | Heart Defects, Congenital - diagnosis | Arrhythmias, Cardiac - complications | Arrhythmias, Cardiac - diagnosis | High-Throughput Nucleotide Sequencing
Journal Article
Journal Article
Journal of Electrocardiology, ISSN 0022-0736, 07/2019, Volume 55, pp. 45 - 50
Brugada phenocopies are Brugada-like ECG patterns induced by reversible clinical conditions. Baranchuk and colleagues characterized this condition in 2012, and... 
Brugada syndrome | Brugada phenocopy | Sudden cardiac death | Channelopathy | ELECTROCARDIOGRAPHIC PATTERN | CARDIAC & CARDIOVASCULAR SYSTEMS | FLECAINIDE | HYPERKALEMIA | TACHYCARDIA | CHALLENGE | ECG PATTERN | PATIENT | ST-SEGMENT ELEVATION | FEVER | Heart | Electrocardiography | Medical colleges | Diagnosis | Arrhythmia | Electrocardiogram
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 09/2017, Volume 128, Issue 9, pp. e259 - e259
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.clinph.2017.07.259 Muscle... 
Electrophysiology | Term stress tests | Channelopathies | Long and short | Paralysis | Diagnosis | Neurophysiology
Journal Article
Gastroenterology, ISSN 0016-5085, 07/2018, Volume 155, Issue 1, pp. 168 - 179
Journal Article