Diana Domingo
Valencia, VC, Spain
Last Updated: 09/26/2026
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Found 12 publications
Genotype FBN1/phenotype relationship in a cohort of patients with Marfan syndrome.
Journal: Clinical genetics
Published: July 02, 2020
Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker.
Journal: Orphanet journal of rare diseases
Published: May 10, 2019
Left ventricular myocardial dysfunction in arrhythmogenic cardiomyopathy with left ventricular involvement: A door to improving diagnosis.
Journal: International journal of cardiology
Published: June 06, 2018
RyR2R420Q catecholaminergic polymorphic ventricular tachycardia mutation induces bradycardia by disturbing the coupled clock pacemaker mechanism.
Journal: JCI insight
Published: December 02, 2016
Deregulated hepatic microRNAs underlie the association between non-alcoholic fatty liver disease and coronary artery disease.
Journal: Liver international : official journal of the International Association for the Study of the Liver
Published: November 15, 2015
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: May 03, 2015
Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study).
Journal: The American journal of cardiology
Published: April 09, 2015
Sensitivity and negative predictive value of treadmill exercise stress testing for the diagnosis of catecholaminergic polymorphic ventricular tachycardia. Response.
Journal: Revista espanola de cardiologia (English ed.)
Published: February 18, 2015
The genetic background of left ventricular hypertrabeculation/noncompaction remains vague. Response.
The genetic background of left ventricular hypertrabeculation/noncompaction remains vague. Response.
Journal: Revista espanola de cardiologia (English ed.)
Published: October 20, 2014
A new mutation in the ryanodine receptor 2 gene (RYR2 C2277R) as a cause catecholaminergic polymorphic ventricular tachycardia.
Journal: Revista espanola de cardiologia (English ed.)
Published: July 21, 2014
Familial left ventricular noncompaction associated with a novel mutation in the alpha-cardiac actin gene.
Journal: Revista espanola de cardiologia (English ed.)
Published: April 04, 2014
Non-ventricular, Clinical, and Functional Features of the RyR2(R420Q) Mutation Causing Catecholaminergic Polymorphic Ventricular Tachycardia.
Journal: Revista espanola de cardiologia (English ed.)
Published: November 22, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026