Cargando…

Sudden cardiac death: focus on the genetics of channelopathies and cardiomyopathies

Sudden cardiac death (SCD) describes a natural and unexpected death from cardiac causes occurring within a short period of time (generally within 1 h of symptom onset) in the absence of any other potentially lethal condition. Most SCD-related diseases have a genetic basis; in particular congenital c...

Descripción completa

Detalles Bibliográficos
Autores principales:	Magi, Simona, Lariccia, Vincenzo, Maiolino, Marta, Amoroso, Salvatore, Gratteri, Santo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556354/ https://www.ncbi.nlm.nih.gov/pubmed/28810874 http://dx.doi.org/10.1186/s12929-017-0364-6

Ejemplares similares

Genetics of channelopathies associated with sudden cardiac death
por: Campuzano, Oscar, et al.
Publicado: (2015)

Editorial: Sudden Cardiac Death and Channelopathies
por: Baltogiannis, Giannis, et al.
Publicado: (2020)

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances
por: Fernández-Falgueras, Anna, et al.
Publicado: (2017)

Intracellular Calcium Dysregulation: Implications for Alzheimer's Disease
por: Magi, Simona, et al.
Publicado: (2016)

Cardiac Ion Channelopathies and the Sudden Infant Death Syndrome
por: Wilders, Ronald
Publicado: (2012)

Identification and functional analysis of a new putative caveolin-3 variant found in a patient with sudden unexplained death
por: Lariccia, Vincenzo, et al.
Publicado: (2014)

Challenges and Opportunities from Targeting Inflammatory Responses to SARS-CoV-2 Infection: A Narrative Review
por: Lariccia, Vincenzo, et al.
Publicado: (2020)

Essential role of the Na(+)-Ca2(+) exchanger (NCX) in glutamate-enhanced cell survival in cardiac cells exposed to hypoxia/reoxygenation
por: Maiolino, Marta, et al.
Publicado: (2017)

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death
por: Coll, Monica, et al.
Publicado: (2017)

Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death
por: Chahine, Mohamed, et al.
Publicado: (2022)

Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death
por: Zaveri, Sahil, et al.
Publicado: (2023)

Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease
por: Martin, Claire A, et al.
Publicado: (2012)

Update on cardiomyopathies and sudden cardiac death
por: Rizzo, Stefania, et al.
Publicado: (2019)

The Multifaced Perspectives of Genetic Testing in Pediatric Cardiomyopathies and Channelopathies
por: Popa-Fotea, Nicoleta-Monica, et al.
Publicado: (2020)

Prospective In Vitro Models of Channelopathies and Cardiomyopathies
por: Kawaguchi, Nanako, et al.
Publicado: (2012)

Drosophila in the Heart of Understanding Cardiac Diseases: Modeling Channelopathies and Cardiomyopathies in the Fruitfly
por: Taghli-Lamallem, Ouarda, et al.
Publicado: (2016)

Computational tools to investigate genetic cardiac channelopathies
por: Abriel, Hugues, et al.
Publicado: (2013)

Risk factors of sudden cardiac death in hypertrophic cardiomyopathy
por: Hong, Ying, et al.
Publicado: (2022)

Defying the Odds of Sudden Cardiac Death in Hypertrophic Cardiomyopathy
por: Rostomian, Ara H., et al.
Publicado: (2020)

Cardiac sodium channelopathies
por: Amin, Ahmad S., et al.
Publicado: (2009)

Excitatory Amino Acid Transporters (EAATs): Glutamate Transport and Beyond
por: Magi, Simona, et al.
Publicado: (2019)

A Review of Catecholamine Associated Cardiomyopathies and Channelopathies
por: Sethi, Pooja, et al.
Publicado: (2020)

Synchronous cardiac arrest in monozygotic twins with hypertrophic cardiomyopathy - Is sudden cardiac death genetically pre-programmed?
por: Goh, Cheng Yee, et al.
Publicado: (2015)

Hypertrophic cardiomyopathy: Sudden cardiac death risk stratification in adults
por: Jordà, Paloma, et al.
Publicado: (2018)

Predictors of Sudden Cardiac Death in Doberman Pinschers with Dilated Cardiomyopathy
por: Klüser, L., et al.
Publicado: (2016)

Hypereosinophilic Syndrome, Cardiomyopathies, and Sudden Cardiac Death in Superinvasive Opisthorchiasis
por: Bychkov, Vitaly G., et al.
Publicado: (2019)

Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies
por: Campuzano, Oscar, et al.
Publicado: (2015)

Prevention of Sudden Cardiac Death in Hypertrophic Cardiomyopathy: What has Changed in The Guidelines?
por: Reis, Liliana, et al.
Publicado: (2018)

Atrial fibrillation in Cardiac Channelopathies
por: Thejus, Jayachandran, et al.
Publicado: (2009)

Inherited arrhythmias: The cardiac channelopathies
por: Behere, Shashank P, et al.
Publicado: (2015)

Cardiac Sympathetic Denervation in Channelopathies
por: Dusi, Veronica, et al.
Publicado: (2019)

Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy
por: Akhtar, M., et al.
Publicado: (2019)

Prevention of Sudden Death in Hypertrophic Cardiomyopathy
por: Arteaga-Fernández, Edmundo, et al.
Publicado: (2018)

Sudden Cardiac Death: A Review Focused on Cardiovascular Imaging
por: Barletta, Valentina, et al.
Publicado: (2014)

Genetic T-type calcium channelopathies
por: Weiss, Norbert, et al.
Publicado: (2020)

Emerging role of genetic analysis for stratification of sudden cardiac death risk in dilated cardiomyopathy: An illustrative case
por: Yao, Jessica Victoria, et al.
Publicado: (2020)

Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies
por: Amarouch, Mohamed-Yassine, et al.
Publicado: (2020)

The omics of channelopathies and cardiomyopathies: what we know and how they are useful
por: Pappone, Carlo, et al.
Publicado: (2020)

Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?
por: Di Resta, Chiara, et al.
Publicado: (2022)

Risk Stratification for Sudden Cardiac Death In Patients With Non-ischemic Dilated Cardiomyopathy
por: Shekha, Karthik, et al.
Publicado: (2005)

Cannot write session to /tmp/vufind_sessions/sess_58t42od0u5gu4tcp710r4c272a