Andrea Aparicio
Oviedo, AS 33011, Spain
Last Updated: 09/26/2026
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Found 9 publications
PCSK9 gene variations in the clinical setting of premature cardiovascular disease: A critical appraisal.
Journal: International journal of cardiology
Published: January 18, 2024
Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry.
Journal: Journal of clinical medicine
Published: June 21, 2023
Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients.
Journal: Journal of clinical medicine
Published: December 31, 2022
Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence.
Journal: Journal of clinical medicine
Published: December 27, 2022
Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia.
Journal: Journal of clinical medicine
Published: December 26, 2022
Slow Coronary Blood Flow: Pathogenesis and Clinical Implications.
Journal: European cardiology
Published: August 31, 2021
Premature STEMI in Men and Women: Current Clinical Features and Improvements in Management and Prognosis.
Journal: Journal of clinical medicine
Published: February 18, 2021
Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome.
Journal: Journal of clinical medicine
Published: October 25, 2020
Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry.
Journal: Journal of clinical medicine
Published: September 03, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026