Ivonne J. Reyes-Cardenas
A Coruna, GA, Spain
Last Updated: 09/26/2026
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Found 9 publications
Genetics in Hypertrophic Cardiomyopathy: An Evolving Clinical Landscape.
Journal: Cardiac failure review
Published: March 31, 2025
TTN cardiomyopathy: expanding clinical relevance beyond the A-band.
Journal: Revista espanola de cardiologia (English ed.)
Published: March 11, 2025
Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.
Journal: Circulation. Genomic and precision medicine
Published: February 14, 2024
The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.
Journal: European journal of medical genetics
Published: May 25, 2020
Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant.
Journal: Revista espanola de cardiologia (English ed.)
Published: May 07, 2020
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy.
Journal: Heart (British Cardiac Society)
Published: March 18, 2020
Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome.
Journal: Revista espanola de cardiologia (English ed.)
Published: November 28, 2018
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
Journal: Journal of the American College of Cardiology
Published: February 25, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026