Julian Reguero-Rodriguez
Av Roma S/N
Oviedo, AS 33011, Spain
Oviedo, AS 33011, Spain
Last Updated: 09/26/2026
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Found 9 publications
Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: a reference unit centre experience.
Journal: European journal of preventive cardiology
Published: August 17, 2023
Association of the Genetic Variation in the Long Non-Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy.
Journal: Life (Basel, Switzerland)
Published: April 04, 2022
The APOB polymorphism rs1801701 A/G (p.R3638Q) is an independent risk factor for early-onset coronary artery disease: Data from a Spanish cohort.
Journal: Nutrition, metabolism, and cardiovascular diseases : NMCD
Published: October 27, 2020
Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders.
Journal: Clinical genetics
Published: September 28, 2020
Congenital long QT syndrome: Should citric fruits be avoided? A case report of a cLQTS type 1 with unusual QTc prolongation with citric juices.
Journal: Journal of cardiology cases
Published: April 07, 2020
IL17RA in early-onset coronary artery disease: Total leukocyte transcript analysis and promoter polymorphism (rs4819554) association.
Journal: Cytokine
Published: March 21, 2020
Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy.
Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research
Published: January 23, 2017
Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope.
Journal: International journal of cardiology
Published: April 12, 2016
New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy.
Journal: Molecular biology reports
Published: January 10, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026