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Journal of the American College of Cardiology, ISSN 0735-1097, 03/2018, Volume 71, Issue 11, pp. 1228 - 1230
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2018, Volume 71, Issue 11, pp. 1228 - 1230
The relationship between channelopathies and sudden infant death syndrome (SIDS) has always been complex and, for reasons that are interesting but would be out... 
mutation | long QT syndrome | genetic testing | neonatal ECG | channelopathies | Electrocardiography | Genetics | Mutation | Sudden infant death syndrome--SIDS | Genomics
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 01/2018, Volume 250, pp. 139 - 145
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A16150 - A16150
IntroductionArrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is an inherited disease characterized by risk for sudden cardiac death (SCD) and fibro-fatty... 
Journal Article
Frontiers in Cardiovascular Medicine, ISSN 2297-055X, 12/2018, Volume 5
In spite of the widespread role of calmodulin (CaM) in cellular signaling, CaM mutations lead specifically to cardiac manifestations, characterized by... 
Phenotype | Arrhythmia | Gene mutations | Genetic aspects | Cellular signal transduction | Research | Calmodulin | repolarization | arrhythmia mechanisms | Ca2+ handling | ion channels | calmodulin mutations
Journal Article
Frontiers in cardiovascular medicine, ISSN 2297-055X, 2018, Volume 5, p. 175
Sudden cardiac death (SCD) in the young may often be the first manifestation of a genetic arrythmogenic disease that had remained undiagnosed. Despite the... 
Cardiomyopathy | Cardiac arrest | Research | Diagnosis | Health aspects | Heart diseases | Calmodulin | CALM | catecholaminergic polymorphic ventricular tachycardia | sudden cardiac death | long QT syndrome | calmodulin
Journal Article
Frontiers in cardiovascular medicine, ISSN 2297-055X, 2018, Volume 5, p. 176
In spite of the widespread role of calmodulin (CaM) in cellular signaling, CaM mutations lead specifically to cardiac manifestations, characterized by... 
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 2009, Volume 145, Issue 1, pp. 45 - 48
Journal Article
Europace, ISSN 1099-5129, 04/2006, Volume 8, Issue 4, pp. 241 - 244
We aimed to verify the tong QT syndrome (LQTS) genotype in a family with strong evidence of LQTS type 1 (LQT1) on the basis of so far established... 
Long QT syndrome | Genotype | Phenotype | Syncope | phenotype | CARDIAC & CARDIOVASCULAR SYSTEMS | HERG | long QT syndrome | GENE | KVLQT1 MUTATIONS | syncope | SPECTRUM | CLINICAL-COURSE | genotype | POTASSIUM CHANNEL | AGE | Greece | KCNQ1 Potassium Channel - genetics | Pedigree | Humans | Electrocardiography | Long QT Syndrome - genetics | Male | Mutation | Child
Journal Article
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