Publicaciones (57) Publicaciones de REBECA LORCA GUTIERREZ

2024

  1. Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening

    Journal of Clinical Medicine, Vol. 13, Núm. 1

  2. Natural History of Dilated Cardiomyopathy Due to c.77T>C (p.Val26Ala) in Emerin Protein

    Journal of Clinical Medicine, Vol. 13, Núm. 3

  3. Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives

    Journal of the American College of Cardiology, Vol. 83, Núm. 17, pp. 1640-1651

  4. “Inherited cardiovascular disease mindset” can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.

    International Journal of Cardiology, Vol. 401

2023

  1. Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry

    Journal of Clinical Medicine, Vol. 12, Núm. 14

  2. Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

    Journal of Clinical Medicine, Vol. 12, Núm. 3

  3. Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence

    Journal of Clinical Medicine, Vol. 12, Núm. 6

  4. Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients

    Journal of Clinical Medicine, Vol. 12, Núm. 3

  5. STEMI in women. Life expectancy recovery after primary percutaneous coronary intervention

    Revista Espanola de Cardiologia, Vol. 76, Núm. 12, pp. 1003-1012

2022

  1. Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy

    Life, Vol. 12, Núm. 6

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

    Life, Vol. 12, Núm. 9

  3. Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort

    CARDIOGENETICS, Vol. 12, Núm. 2, pp. 198-205

  4. KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

    Life, Vol. 12, Núm. 4

  5. Natural History of MYH7-Related Dilated Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 80, Núm. 15, pp. 1447-1461

  6. Permanent Pacemaker Reduction Using Cusp-Overlapping Projection in TAVR: A Propensity Score Analysis

    JACC: Cardiovascular Interventions, Vol. 15, Núm. 2, pp. 150-161

2021

  1. Coexistence of transmural and lateral wavefront progression of myocardial infarction in the human heart

    Revista Espanola de Cardiologia, Vol. 74, Núm. 10, pp. 870-877

  2. Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

    Clinical Genetics, Vol. 99, Núm. 3, pp. 457-461

  3. Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The CARDIO-SOR study

    Liver International, Vol. 41, Núm. 9, pp. 2200-2211

  4. Founder mutation in myosin-binding protein C with an early onset and a high penetrance in males

    Open Heart, Vol. 8, Núm. 2

  5. Frailty assessment in a cohort of elderly patients with severe symptomatic aortic stenosis: Insights from the frailty evaluation in severe aortic stenosis (fresas) registry

    Journal of Clinical Medicine, Vol. 10, Núm. 11