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Ultrasound in Medicine & Biology|January 21, 2012
Ultrasound markers that describe plaques are more sensitive than mean intima-media thickness in patients with familial hypercholesterolemiaAlexandra I Ershova, Tatyana V Balakhonova, Alexey N Meshkov, et al.
Frontiers in Cardiovascular Medicine|February 4, 2021
Case Report: Hypertriglyceridemia and Premature Atherosclerosis in a Patient With Apolipoprotein E Gene ε2ε1 GenotypeAlena S Limonova, Alexandra I Ershova, Alexey N Meshkov, et al.
Frontiers in Cardiovascular Medicine|January 31, 2022
Case Report: Next Generation Sequencing in Clinical Practice-A Real Tool for Ending the Protracted Diagnostic OdysseyAlena S Limonova, Alexandra I Ershova, Alexey N Meshkov, et al.
Circulation. Genomic and Precision Medicine|March 28, 2025
On Penetrance Estimation in Family, Clinical, and Population CohortsMarija Zaicenoka, Vasily E Ramensky, Anna V Kiseleva, et al.
Plos One|July 20, 2016
Carotid and Aortic Stiffness in Patients with Heterozygous Familial HypercholesterolemiaAlexandra I Ershova, Alexey N Meshkov, Tatyana A Rozhkova, et al.
Journal of Personalized Medicine|June 2, 2021
The Prevalence of Heterozygous Familial Hypercholesterolemia in Selected Regions of the Russian Federation: The FH-ESSE-RF StudyAlexey N Meshkov, Alexandra I Ershova, Anna V Kiseleva, et al.
Frontiers in Cardiovascular Medicine|September 12, 2022
Phenotypic vs. genetic cascade screening for familial hypercholesterolemia: A case reportAnastasia V Blokhina, Alexandra I Ershova, Alexey N Meshkov, et al.
Journal of Clinical Medicine|January 8, 2025
Exploring the Link Between Interoception and Symptom Severity in Premature Ventricular ContractionsAlena S Limonova, Irina A Minenko, Anastasia A Sukmanova, et al.
International Journal of Molecular Sciences|September 9, 2023
Applicability of Diagnostic Criteria and High Prevalence of Familial Dysbetalipoproteinemia in Russia: A Pilot StudyAnastasia V Blokhina, Alexandra I Ershova, Anna V Kiseleva, et al.
Biomedicines|April 29, 2025
A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico AnalysisAnna A Bukaeva, Anastasia V Blokhina, Maria S Kharlap, et al.
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