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List of works by 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 ⬇️

scientific article published on October 1, 2012

Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome

scientific article published on 15 February 2014

Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia

scientific article

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.

scientific article published on 12 May 2005

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

scientific article published on 05 December 2018

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

scientific article published on 01 September 2019

Catecholaminergic Polymorphic Ventricular Tachycardia

scientific article published in December 2010

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

scientific article

Controversies in Brugada syndrome

scientific article published on 27 November 2017

Desmosomal junctions are necessary for adult sinus node function.

scientific article published on 20 April 2016

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

scientific article (publication date: July 2014)

Discerning From the Good, the Bad, and the Ugly

scientific article

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

scientific article published on 16 December 2016

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

scientific article published on 10 May 2017

Electrocardiographic features of sudden unexpected death in epilepsy

scientific article published on 24 May 2016

Exercise: A Risky Subject in Arrhythmogenic Cardiomyopathy

scientific article published on 16 June 2018

Experimental therapy of genetic arrhythmias: disease-specific pharmacology.

scientific article

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

scientific article published on 01 January 2005

Genetic arrhythmias.

scientific article

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.

scientific article published in December 2005

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

scientific article

Genetics of ion-channel disorders.

scientific article published on May 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

scientific article published on 08 May 2019

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

scientific article published on 01 October 2018

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

scientific article published on 25 February 2013

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

scientific article published on 29 March 2004

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

scientific article

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

scientific article published in January 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.

scientific article published on 24 July 2017

Pleiotropic Phenotypes Associated With PKP2 Variants

scientific article published on 18 December 2018

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

scientific article published on April 2016

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

scientific article published on February 10, 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.

scientific article

Universal scaling law of electrical turbulence in the mammalian heart

scholarly article

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

scientific article published on 9 November 2006

[Brugada's syndrome]

scientific article published on 01 October 2003

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