Lista de obras - Marina Cerrone - Dominio Público Uruguay

4965Non-transcriptional disruption of Ca2+i homeostasis and Cx43 function in the right ventricle precedes overt arrhythmogenic cardiomyopathy in PKP2-deficient mice

A Clinical Approach to Inherited Arrhythmias ⬇️

artículo científico publicado el 1 de octubre de 2012

Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome

artículo científico

Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2007

Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders

scientific article published on 12 August 2019

Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor.

artículo científico publicado en 2005

Blockade of the Adenosine 2A Receptor Mitigates the Cardiomyopathy Induced by Loss of Plakophilin-2 Expression

scientific article published on 05 December 2018

Brugada's syndrome

scientific article published on 01 October 2003

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

scientific article published on 01 September 2019

Catecholaminergic Polymorphic Ventricular Tachycardia

artículo científico publicado en 2010

Connexin43 contributes to electrotonic conduction across scar tissue in the intact heart.

artículo científico publicado en 2016

Controversies in Brugada syndrome

artículo científico publicado en 2017

Desmosomal junctions are necessary for adult sinus node function.

artículo científico publicado en 2016

Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome

artículo científico publicado en 2014

Discerning From the Good, the Bad, and the Ugly

artículo científico publicado en 2017

Disruption of Ca2+i Homeostasis and Connexin 43 Hemichannel Function in the Right Ventricle Precedes Overt Arrhythmogenic Cardiomyopathy in Plakophilin-2-Deficient Mice

scientific article published on 18 July 2019

ECG non-specific ST-T and QTc abnormalities in patients with systemic lupus erythematosus compared with rheumatoid arthritis

artículo científico publicado en 2016

Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial

artículo científico publicado en 2017

Electrocardiographic features of sudden unexpected death in epilepsy

artículo científico publicado en 2016

Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy

scientific article published on 16 June 2018

Experimental therapy of genetic arrhythmias: disease-specific pharmacology.

artículo científico publicado en 2006

Fast-slow and slow-slow form of atrioventricular nodal reentrant tachycardia sustained by the same reentrant circuit: a case report

artículo científico publicado en 2005

Genetic arrhythmias.

artículo científico publicado en 2005

Genetic testing for inherited cardiac arrhythmias.

scientific article published on March 2010

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

artículo científico publicado en 2005

Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias.

artículo científico publicado en 2014

Genetics of ion-channel disorders.

artículo científico publicado en 2012

Genetics of sudden death: focus on inherited channelopathies.

scientific article published on 09 April 2011

Impact of RNA testing on cardiac variant interpretation and patient management

artículo científico publicado en 2019

Implantable Loop Recorder in Inherited Arrhythmia Diseases: A Critical Tool for Symptom Diagnosis and Advanced Risk Stratification

artículo científico publicado en 2018

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

artículo científico publicado en 2013

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

artículo científico publicado en 2004

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype

artículo científico publicado en 2014

Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family

article

Molecular genetics: is it making an impact in the management of inherited arrhythmogenic syndromes?

article

Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis

artículo científico publicado en 2017

Multimodality Imaging of Danon Disease in a Patient with a Novel LAMP2 Mutation

scientific article published on 21 June 2019

Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young

scientific article published on 01 November 2018

Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm.

artículo científico publicado en 2017

Pleiotropic Phenotypes Associated With PKP2 Variants

artículo científico publicado en 2018

Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications.

artículo científico publicado en 2016

Risk indicators in long QT syndrome: Does location matter? ⬇️

artículo científico publicado el 10 de febrero de 2012

Routine electrocardiogram and medical history in syncope: a simple approach can identify most high-risk patients

scientific article published on 25 August 2009

Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.

artículo científico publicado en 2012

Universal scaling law of electrical turbulence in the mammalian heart

artículo científico publicado en 2007

Up-regulation of the inward rectifier K+ current (I K1) in the mouse heart accelerates and stabilizes rotors

artículo científico publicado en 2006

Lista de obras de Marina Cerrone

4965Non-transcriptional disruption of Ca2+i homeostasis and Cx43 function in the right ventricle precedes overt arrhythmogenic cardiomyopathy in PKP2-deficient mice

A Clinical Approach to Inherited Arrhythmias ⬇️

Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome

Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia

Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders

Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor.

Blockade of the Adenosine 2A Receptor Mitigates the Cardiomyopathy Induced by Loss of Plakophilin-2 Expression

Brugada's syndrome

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Catecholaminergic Polymorphic Ventricular Tachycardia

Connexin43 contributes to electrotonic conduction across scar tissue in the intact heart.

Controversies in Brugada syndrome

Desmosomal junctions are necessary for adult sinus node function.

Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome

Discerning From the Good, the Bad, and the Ugly

Disruption of Ca2+i Homeostasis and Connexin 43 Hemichannel Function in the Right Ventricle Precedes Overt Arrhythmogenic Cardiomyopathy in Plakophilin-2-Deficient Mice

ECG non-specific ST-T and QTc abnormalities in patients with systemic lupus erythematosus compared with rheumatoid arthritis

Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial

Electrocardiographic features of sudden unexpected death in epilepsy

Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy

Experimental therapy of genetic arrhythmias: disease-specific pharmacology.

Fast-slow and slow-slow form of atrioventricular nodal reentrant tachycardia sustained by the same reentrant circuit: a case report

Genetic arrhythmias.

Genetic testing for inherited cardiac arrhythmias.

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias.

Genetics of ion-channel disorders.

Genetics of sudden death: focus on inherited channelopathies.

Impact of RNA testing on cardiac variant interpretation and patient management

Implantable Loop Recorder in Inherited Arrhythmia Diseases: A Critical Tool for Symptom Diagnosis and Advanced Risk Stratification

KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype

Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family

Molecular genetics: is it making an impact in the management of inherited arrhythmogenic syndromes?

Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis

Multimodality Imaging of Danon Disease in a Patient with a Novel LAMP2 Mutation

Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young

Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm.

Pleiotropic Phenotypes Associated With PKP2 Variants

Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications.

Risk indicators in long QT syndrome: Does location matter? ⬇️

Routine electrocardiogram and medical history in syncope: a simple approach can identify most high-risk patients

Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.

Universal scaling law of electrical turbulence in the mammalian heart

Up-regulation of the inward rectifier K+ current (I K1) in the mouse heart accelerates and stabilizes rotors