Maria D. Di Taranto

Via Gaetano Salvatore 486
Naples, 80145, Italy

Last Updated: 09/26/2026

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Found 44 publications

Genetic Influence on LDL-Cholesterol Levels: Role of Polygenic Risk Scores and Lp(a) Beyond Monogenic Hypercholesterolemia.

Genetic Influence on LDL-Cholesterol Levels: Role of Polygenic Risk Scores and Lp(a) Beyond Monogenic Hypercholesterolemia.

Journal: Genes

Published: May 08, 2026

Real-world lipid outcomes after switching PCSK9-targeting therapies in heterozygous familial hypercholesterolemia: the SHIFT-FH study.

Real-world lipid outcomes after switching PCSK9-targeting therapies in heterozygous familial hypercholesterolemia: the SHIFT-FH study.

Journal: Internal and emergency medicine

Published: March 23, 2026

Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score.

Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score.

Journal: Genes

Published: January 14, 2026

Lipidomic Signature of Patients with Familial Hypercholesterolemia Carrying Pathogenic Variants Unveils a Cue of Increased Cardiovascular Risk.

Lipidomic Signature of Patients with Familial Hypercholesterolemia Carrying Pathogenic Variants Unveils a Cue of Increased Cardiovascular Risk.

Journal: International journal of molecular sciences

Published: September 27, 2025

Genetic Assessment and Clinical Correlates in Severe Hypertriglyceridemia: A Systematic Review.

Genetic Assessment and Clinical Correlates in Severe Hypertriglyceridemia: A Systematic Review.

Journal: Genes

Published: September 22, 2025

A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease.

A delayed diagnosis of familial chylomicronemia syndrome in an elderly patient: Clinical implications of late-onset disease.

Journal: Journal of clinical lipidology

Published: August 15, 2025

The lysosomal acid lipase deficiency spectrum from infancy to adulthood: a multidisciplinary experience.

The lysosomal acid lipase deficiency spectrum from infancy to adulthood: a multidisciplinary experience.

Journal: Nutrition, metabolism, and cardiovascular diseases : NMCD

Published: May 16, 2025

Evinacumab for Homozygous Familial Hypercholesterolemia: The Italian Cohort of the ELIPSE HoFH Study.

Evinacumab for Homozygous Familial Hypercholesterolemia: The Italian Cohort of the ELIPSE HoFH Study.

Journal: Advances in therapy

Published: December 04, 2024

New insights into the management of homozygous familial hypercholesterolemia patients treated with lomitapide: a single-center experience.

New insights into the management of homozygous familial hypercholesterolemia patients treated with lomitapide: a single-center experience.

Journal: Frontiers in endocrinology

Published: October 23, 2024

Assessment of Platelet Aggregation and Thrombin Generation in Patients with Familial Chylomicronemia Syndrome Treated with Volanesorsen: A Cross-Sectional Study.

Assessment of Platelet Aggregation and Thrombin Generation in Patients with Familial Chylomicronemia Syndrome Treated with Volanesorsen: A Cross-Sectional Study.

Journal: Biomedicines

Published: July 03, 2024

Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome.

Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome.

Journal: Genes

Published: June 21, 2024

Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia.

Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia.

Journal: Genes

Published: March 08, 2024

Showing 1-12 of 44

Last Updated: 09/26/2026