Found: 62
Select item for more details and to access through your institution.
Genetic testing for inherited arrhythmia syndromes and cardiomyopathies: results of the European Heart Rhythm Association survey.
- Published in:
- EP: Europace, 2024, v. 26, n. 9, p. 1, doi. 10.1093/europace/euae216
- By:
- Publication type:
- Article
From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies.
- Published in:
- EP: Europace, 2023, v. 25, n. 8, p. 1, doi. 10.1093/europace/euad180
- By:
- Publication type:
- Article
Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2.
- Published in:
- EP: Europace, 2023, v. 25, n. 5, p. 1, doi. 10.1093/europace/euad094
- By:
- Publication type:
- Article
From gene-specific to function-specific risk stratification in long QT syndrome Type 2: implications for clinical management.
- Published in:
- EP: Europace, 2023, v. 25, n. 4, p. 1320, doi. 10.1093/europace/euad035
- By:
- Publication type:
- Article
European Society of Cardiology quality indicators for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed in collaboration with the European Heart Rhythm Association of the European Society of Cardiology
- Published in:
- EP: Europace, 2023, v. 25, n. 1, p. 199, doi. 10.1093/europace/euac114
- By:
- Publication type:
- Article
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Brugada syndrome and syncope: a practical approach for diagnosis and treatment.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Infanticide vs. inherited cardiac arrhythmias.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Congenital long QT syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Congenital long QT syndrome.
- Published in:
- Orphanet Journal of Rare Diseases, 2008, v. 3, p. 1, doi. 10.1186/1750-1172-3-18
- By:
- Publication type:
- Article
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Mitochondrial a Kinase Anchor Proteins in Cardiovascular Health and Disease: A Review Article on Behalf of the Working Group on Cellular and Molecular Biology of the Heart of the Italian Society of Cardiology.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 14, p. 7691, doi. 10.3390/ijms23147691
- By:
- Publication type:
- Article
Novel Basic Science Insights to Improve the Management of Heart Failure: Review of the Working Group on Cellular and Molecular Biology of the Heart of the Italian Society of Cardiology.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1192, doi. 10.3390/ijms21041192
- By:
- Publication type:
- Article
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Adenosine and the Cardiovascular System: The Good and the Bad.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 5, p. 1366, doi. 10.3390/jcm9051366
- By:
- Publication type:
- Article
Cardiogenetics: An Open Access Journal.
- Published in:
- Cardiogenetics, 2020, v. 10, n. 2, p. 42, doi. 10.3390/cardiogenetics10020008
- By:
- Publication type:
- Article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
- Published in:
- Nature Genetics, 2014, v. 46, n. 8, p. 826, doi. 10.1038/ng.3014
- By:
- Publication type:
- Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1409, doi. 10.1038/ng1113-1409b
- By:
- Publication type:
- Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
- Published in:
- Nature Genetics, 2013, v. 45, n. 9, p. 1044, doi. 10.1038/ng.2712
- By:
- Publication type:
- Article
Corrigendum: Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.
- Published in:
- Scientific Reports, 2016, p. 25863, doi. 10.1038/srep25863
- By:
- Publication type:
- Article
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.
- Published in:
- Scientific Reports, 2016, p. 22235, doi. 10.1038/srep22235
- By:
- Publication type:
- Article
Multiscale Complexity Analysis of the Cardiac Control Identifies Asymptomatic and Symptomatic Patients in Long QT Syndrome Type 1.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093808
- By:
- Publication type:
- Article
Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation.
- Published in:
- European Heart Journal, 2024, v. 45, n. 29, p. 2647, doi. 10.1093/eurheartj/ehae289
- By:
- Publication type:
- Article
Calmodulin, sudden death, and the Folbigg case: genes in court.
- Published in:
- European Heart Journal, 2024, v. 45, n. 20, p. 1801, doi. 10.1093/eurheartj/ehae152
- By:
- Publication type:
- Article
Implantable loop recorders in patients with Brugada syndrome: the BruLoop study.
- Published in:
- European Heart Journal, 2024, v. 45, n. 14, p. 1255, doi. 10.1093/eurheartj/ehae133
- By:
- Publication type:
- Article
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
- Published in:
- European Heart Journal, 2023, v. 44, n. 35, p. 3357, doi. 10.1093/eurheartj/ehad418
- By:
- Publication type:
- Article
When prescribing drugs, do medical doctors and healthcare professionals realize that their patient has the long QT syndrome?
- Published in:
- European Heart Journal, 2019, v. 40, n. 37, p. 3118, doi. 10.1093/eurheartj/ehz355
- By:
- Publication type:
- Article
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.
- Published in:
- European Heart Journal, 2019, v. 40, n. 35, p. 2964, doi. 10.1093/eurheartj/ehz311
- By:
- Publication type:
- Article
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2.
- Published in:
- European Heart Journal, 2019, v. 40, n. 23, p. 1832, doi. 10.1093/eurheartj/ehz023
- By:
- Publication type:
- Article
Modifier genes for sudden cardiac death.
- Published in:
- European Heart Journal, 2018, v. 39, n. 44, p. 3925, doi. 10.1093/eurheartj/ehy502
- By:
- Publication type:
- Article
Circadian and Seasonal Pattern of Arrhythmic Events in Arrhythmogenic Cardiomyopathy Patients.
- Published in:
- International Journal of Environmental Research & Public Health, 2023, v. 20, n. 4, p. 2872, doi. 10.3390/ijerph20042872
- By:
- Publication type:
- Article
Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked Questions.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 7, p. 2489, doi. 10.3390/jcm12072489
- By:
- Publication type:
- Article
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.
- Published in:
- Journal of Arrhythmia, 2022, v. 38, n. 4, p. 491, doi. 10.1002/joa3.12717
- By:
- Publication type:
- Article
Executive Attentional Dyscontrol as a Core Cognitive and Behavioral Feature of Individuals with Obesity and Cardiovascular Disease: A Cross-Sectional Investigation.
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 8, p. 1182, doi. 10.3390/brainsci13081182
- By:
- Publication type:
- Article
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability.
- Published in:
- Cardiovascular Research, 2017, v. 113, n. 10, p. 1256, doi. 10.1093/cvr/cvx122
- By:
- Publication type:
- Article
Elucidating arrhythmogenicmechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes.
- Published in:
- Cardiovascular Research, 2017, v. 113, n. 5, p. 531, doi. 10.1093/cvr/cvx006
- By:
- Publication type:
- Article
Current gaps in knowledge in inherited arrhythmia syndromes.
- Published in:
- Netherlands Heart Journal, 2023, v. 31, n. 7/8, p. 272, doi. 10.1007/s12471-023-01797-w
- By:
- Publication type:
- Article
MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes.
- Published in:
- Cardiovascular Research, 2021, v. 117, n. 3, p. 767, doi. 10.1093/cvr/cvaa019
- By:
- Publication type:
- Article
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis.
- Published in:
- Cardiovascular Research, 2021, v. 117, n. 2, p. 472, doi. 10.1093/cvr/cvaa036
- By:
- Publication type:
- Article
Heritable arrhythmias associated with abnormal function of cardiac potassium channels.
- Published in:
- Cardiovascular Research, 2020, v. 116, n. 9, p. 1542, doi. 10.1093/cvr/cvaa068
- By:
- Publication type:
- Article
Unmasking the prevalence of amyloid cardiomyopathy in the real world: results from Phase 2 of the AC‐TIVE study, an Italian nationwide survey.
- Published in:
- European Journal of Heart Failure, 2022, v. 24, n. 8, p. 1377, doi. 10.1002/ejhf.2504
- By:
- Publication type:
- Article
Indications and utility of cardiac genetic testing in athletes.
- Published in:
- European Journal of Preventive Cardiology, 2022, v. 29, n. 12, p. 1582, doi. 10.1093/eurjpc/zwac080
- By:
- Publication type:
- Article
national survey on prevalence of possible echocardiographic red flags of amyloid cardiomyopathy in consecutive patients undergoing routine echocardiography: study design and patients characterization — the first insight from the AC-TIVE Study.
- Published in:
- European Journal of Preventive Cardiology, 2022, v. 29, n. 5, p. e173, doi. 10.1093/eurjpc/zwab127
- By:
- Publication type:
- Article
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivors.
- Published in:
- European Journal of Preventive Cardiology, 2021, v. 28, n. 10, p. 1134, doi. 10.1177/2047487320940863
- By:
- Publication type:
- Article
To be, or not to be engaged in sport activities, that is the amletic question for patients with coronary artery disease.
- Published in:
- 2020
- By:
- Publication type:
- Editorial
COVID-19 pandemia and inherited cardiomyopathies and channelopathies: a short term and long term perspective.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Current patterns of beta‐blocker prescription in cardiac amyloidosis: an Italian nationwide survey.
- Published in:
- ESC Heart Failure, 2021, v. 8, n. 4, p. 3369, doi. 10.1002/ehf2.13411
- By:
- Publication type:
- Article
Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families.
- Published in:
- Journal of the American Heart Association, 2023, v. 12, n. 17, p. 1, doi. 10.1161/JAHA.122.029100
- By:
- Publication type:
- Article
Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanisms.
- Published in:
- 2014
- By:
- Publication type:
- journal article