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The New England Journal of Medicine, ISSN 0028-4793, 10/2010, Volume 363, Issue 15, pp. 1397 - 1409
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 01/2019, Volume 274, pp. 190 - 191
Journal Article
Circulation, ISSN 0009-7322, 2012, Volume 125, Issue 16, pp. 1988 - +
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 2007, Volume 115, Issue 19, pp. 2481 - 2489
BACKGROUND: Type-1 long-QT syndrome (LQTS) is caused by loss-of-function mutations in the KCNQ1-encoded I(Ks) cardiac potassium channel. We evaluated the... 
Electrocardiography | Genetics | Long-QT syndrome | MUTANT | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIAC-ARRHYTHMIA | RISK | SUPPRESSION | long-QT syndrome | electrocardiography | genetics | HERG | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | POTASSIUM CHANNEL | LQT1 FORM | AGE | Potassium - metabolism | Japan - epidemiology | Sequence Deletion | United States - epidemiology | Frameshift Mutation | KCNQ1 Potassium Channel - genetics | Syncope - epidemiology | Death, Sudden, Cardiac - epidemiology | Humans | Netherlands - epidemiology | Child, Preschool | Death, Sudden, Cardiac - prevention & control | Infant | Male | Mutation, Missense | Romano-Ward Syndrome - mortality | Romano-Ward Syndrome - drug therapy | KCNQ1 Potassium Channel - chemistry | Adult | Female | Registries | Child | Romano-Ward Syndrome - genetics | Infant, Newborn | Adrenergic beta-Antagonists - therapeutic use | Protein Structure, Tertiary | Genetic Predisposition to Disease | RNA Splice Sites - genetics | Risk Factors | Romano-Ward Syndrome - complications | Heart Arrest - epidemiology | Kaplan-Meier Estimate | Proportional Hazards Models | KCNQ1 Potassium Channel - physiology | Models, Molecular | Genotype | Codon, Nonsense | Protein Transport | Phenotype | Membrane Potentials | Adolescent | Mutagenesis, Insertional | Mutation | Ion Transport - genetics | Long QT syndrome | Physiological aspects | Ion channels | Research | Gene mutations | Risk factors
Journal Article
Iranian biomedical journal, ISSN 1028-852X, 05/2019, Volume 23, Issue 3, pp. 228 - 234
Long QT syndrome (LQTS) is characterized by the prolongation of QT interval, which results in syncope and sudden cardiac death in young people. KCNQ1 is the... 
Long QT syndrome | Romano-Ward syndrome | KCNQ1 | Short Communication | Jervell-Lange-Nielsen syndrome
Journal Article
Cardiovascular Research, ISSN 0008-6363, 09/2012, Volume 95, Issue 4, pp. 419 - 429
Long QT syndrome (LQTS) is an inheritable and life-threatening disease; however, it is often difficult to determine disease characteristics in sporadic cases... 
Long QT syndrome | Cardiomyocytes | Personalized medicine | Drug examination | iPS cells | CARDIAC & CARDIOVASCULAR SYSTEMS | MODELS | DEATH | LONG-QT SYNDROME | REPOLARIZATION RESERVE | I-KS | KCNQ1 Potassium Channel - genetics | Intermediate-Conductance Calcium-Activated Potassium Channels - genetics | Coculture Techniques | Humans | KCNQ1 Potassium Channel - metabolism | Romano-Ward Syndrome - pathology | Male | Intermediate-Conductance Calcium-Activated Potassium Channels - metabolism | Cellular Reprogramming | Teratoma - metabolism | Action Potentials | Embryoid Bodies - metabolism | Transfection | Potassium Channels, Voltage-Gated - metabolism | Time Factors | Gene Expression Regulation, Developmental | HEK293 Cells | Intermediate-Conductance Calcium-Activated Potassium Channels - antagonists & inhibitors | KCNQ1 Potassium Channel - antagonists & inhibitors | Cell Differentiation | Romano-Ward Syndrome - genetics | Potassium Channel Blockers - pharmacology | Induced Pluripotent Stem Cells - metabolism | Potassium Channels, Voltage-Gated - genetics | Induced Pluripotent Stem Cells - pathology | Genetic Predisposition to Disease | Induced Pluripotent Stem Cells - drug effects | Romano-Ward Syndrome - diagnosis | Induced Pluripotent Stem Cells - transplantation | Embryoid Bodies - pathology | Potassium Channels, Voltage-Gated - antagonists & inhibitors | Myocytes, Cardiac - pathology | Myocytes, Cardiac - transplantation | Patch-Clamp Techniques | Phenotype | Teratoma - pathology | Animals | Myocytes, Cardiac - drug effects | Adolescent | Fluorescent Antibody Technique | Romano-Ward Syndrome - metabolism | Myocytes, Cardiac - metabolism | Mice
Journal Article
Paediatrica Indonesiana, ISSN 0030-9311, 12/2018, Volume 34, Issue 7-8, pp. 221 - 30
We report a case o fhereditary long Q-T syndrome without congenital deafness (Romano-Ward syndrome). In four members of a family, a father and his daughters,... 
hereditary long Q-T; Romano-Ward syndrome; congenital deafness
Journal Article
British Journal of Anaesthesia, ISSN 0007-0912, 04/2018, Volume 120, Issue 4, pp. 629 - 644
Journal Article