REBECA
LORCA GUTIERREZ
Profesora Asociada en CC. Salud - LOSU
Hospital Universitario Central de Asturias
Oviedo, EspañaHospital Universitario Central de Asturias -ko ikertzaileekin lankidetzan egindako argitalpenak (50)
2024
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Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening
Journal of Clinical Medicine, Vol. 13, Núm. 1
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Natural History of Dilated Cardiomyopathy Due to c.77T>C (p.Val26Ala) in Emerin Protein
Journal of Clinical Medicine, Vol. 13, Núm. 3
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Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
Journal of the American College of Cardiology, Vol. 83, Núm. 17, pp. 1640-1651
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Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: a reference unit centre experience
European Journal of Preventive Cardiology, Vol. 31, Núm. 6, pp. e38-e41
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Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing
International Journal of Cardiology, Vol. 408
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“Inherited cardiovascular disease mindset” can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.
International Journal of Cardiology, Vol. 401
2023
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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
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Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
Journal of Clinical Medicine, Vol. 12, Núm. 3
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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
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Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
Journal of Clinical Medicine, Vol. 12, Núm. 3
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STEMI in women. Life expectancy recovery after primary percutaneous coronary intervention
Revista Espanola de Cardiologia, Vol. 76, Núm. 12, pp. 1003-1012
2022
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Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 6
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Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 9
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KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort
Life, Vol. 12, Núm. 4
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Natural History of MYH7-Related Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 80, Núm. 15, pp. 1447-1461
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Permanent Pacemaker Reduction Using Cusp-Overlapping Projection in TAVR: A Propensity Score Analysis
JACC: Cardiovascular Interventions, Vol. 15, Núm. 2, pp. 150-161
2021
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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
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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
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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
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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