Argitalpenak (89) ROCIO TORO CEBADA argitalpenak

filter_list

2025

  1. Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes

    iScience, Vol. 28, Núm. 5

  2. MicroRNA-143-3p and miR-452-5p: A Fingerprint for the Diagnosis of Aortic Stenosis in the Geriatric Population

    Biomedicines, Vol. 13, Núm. 3

  3. MicroRNAs unlock mystery of arrhythmogenic cardiomyopathy

    Kardiologia Polska

2024

  1. A narrative review of inherited arrhythmogenic syndromes in young population: Role of genetic diagnosis in exercise recommendations

    BMJ Open Sport and Exercise Medicine, Vol. 10, Núm. 3

  2. Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis

    Biomedicines, Vol. 12, Núm. 11

  3. Coronary Flow Reserve and Myocardial Resistance Reserve Changes After Transcatheter Aortic Valve Implantation in Aortic Stenosis

    American Journal of Cardiology, Vol. 214, pp. 109-114

  4. Exploring miRNA–target gene pair detection in disease with coRmiT

    Briefings in Bioinformatics, Vol. 25, Núm. 2

  5. Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

    International Journal of Molecular Sciences, Vol. 25, Núm. 7

  6. Interpreting the actionable clinical role of rare variants associated with short QT syndrome

    Human Genetics, Vol. 143, Núm. 12, pp. 1499-1508

  7. Role of miRNA–mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy

    Biomedicines, Vol. 12, Núm. 8

  8. The Protective Role of miR-130b-3p Against Palmitate-Induced Lipotoxicity in Cardiomyocytes Through PPARγ Pathway

    International Journal of Molecular Sciences, Vol. 25, Núm. 22

  9. Unraveling the Etiology of Dilated Cardiomyopathy through Differential miRNA–mRNA Interactome

    Biomolecules, Vol. 14, Núm. 5

2023

  1. Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death

    Frontiers in Medicine, Vol. 10

  2. Next-generation sequencing reveals genetic differences between two distinct etiologies of dilated cardiomyopathy

    Atherosclerosis, Vol. 379, pp. S179

  3. Prevalence of transthyretin cardiac amyloidosis in elderly patients diagnosed with heart failure

    Revista Espanola de Geriatria y Gerontologia, Vol. 58, Núm. 1, pp. 8-14

  4. Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort

    International Journal of Legal Medicine, Vol. 137, Núm. 2, pp. 345-351

  5. Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice

    Translational Research, Vol. 259, pp. 72-82

  6. Transcriptome analysis of miRNA and mRNA in the myocardial tissue of mice with LMNA-dilated cardiomyopathy

    Atherosclerosis, Vol. 379, pp. S179-S180

  7. Value of NT-proBNP and Galectin-3 as Biomarkers in the Follow-Up of Asymptomatic Elderly Patients with Severe Aortic Stenosis

    Journal of Clinical Medicine, Vol. 12, Núm. 8

  8. Volumetric quantification of coronary steal in a giant coronary fistula

    Revista Espanola de Cardiologia, Vol. 76, Núm. 8, pp. 664