Jose J. Reguero-Rodriguez

Oviedo, AS 33011, Spain

Last Updated: 09/26/2026

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Found 12 publications

Familial Short QT Syndrome: Phenotypic Variability and Challenges in Risk Stratification.

Familial Short QT Syndrome: Phenotypic Variability and Challenges in Risk Stratification.

Journal: Journal of clinical medicine

Published: March 17, 2026

A New High Penetrant Intronic Pathogenic Variant Related to Long QT Syndrome Type 2.

A New High Penetrant Intronic Pathogenic Variant Related to Long QT Syndrome Type 2.

Journal: Journal of clinical medicine

Published: May 07, 2025

Myosin inhibitors in obstructive hypertrophic cardiomyopathy.

Myosin inhibitors in obstructive hypertrophic cardiomyopathy.

Journal: Medicina clinica

Published: December 11, 2024

Epigenetic Study of Cohort of Monozygotic Twins With Hypertrophic Cardiomyopathy Due to MYBPC3 (Cardiac Myosin-Binding Protein C).

Epigenetic Study of Cohort of Monozygotic Twins With Hypertrophic Cardiomyopathy Due to MYBPC3 (Cardiac Myosin-Binding Protein C).

Journal: Journal of the American Heart Association

Published: October 29, 2024

Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy.

Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy.

Journal: Life (Basel, Switzerland)

Published: July 21, 2022

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome.

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome.

Journal: Journal of clinical medicine

Published: October 25, 2020

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry.

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry.

Journal: Journal of clinical medicine

Published: September 03, 2020

Characterization of Left Ventricular Non-Compaction Cardiomyopathy.

Characterization of Left Ventricular Non-Compaction Cardiomyopathy.

Journal: Journal of clinical medicine

Published: June 15, 2020

Pregnancy and Cardiac Disease: Making Headway.

Pregnancy and Cardiac Disease: Making Headway.

Journal: Revista espanola de cardiologia (English ed.)

Published: February 12, 2017

Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival.

Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival.

Journal: Revista espanola de cardiologia (English ed.)

Published: January 18, 2017

Founder mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 gene in iberian romani patients with pulmonary veno-occlusive disease: A warning for our daily practice.

Founder mutation C.3344C>t(p.Pro1115Leu) in the EIF2KA4 gene in iberian romani patients with pulmonary veno-occlusive disease: A warning for our daily practice.

Journal: Archivos de bronconeumologia

Published: November 16, 2015

Reversible pre-capillary pulmonary hypertension due to dasatinib.

Reversible pre-capillary pulmonary hypertension due to dasatinib.

Journal: Respiratory care

Published: October 24, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026