[HTML][HTML] Galectin-3 in cardiovascular diseases

V Blanda, UM Bracale, MD Di Taranto… - International journal of …, 2020 - mdpi.com
Galectin-3 (Gal-3) is a β-galactoside-binding protein belonging to the lectin family with
pleiotropic regulatory activities and several physiological cellular functions, such as cellular …

Paediatric familial hypercholesterolaemia screening in Europe: public policy background and recommendations

SS Gidding, A Wiegman, U Groselj… - European journal of …, 2022 - academic.oup.com
Familial hypercholesterolaemia (FH) is under-recognized and under-treated in Europe
leading to significantly higher risk for premature heart disease in those affected. As treatment …

Overview of the current status of familial hypercholesterolaemia care in over 60 countries-The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

AJ Vallejo-Vaz, M De Marco, CAT Stevens, A Akram… - Atherosclerosis, 2018 - Elsevier
Background and aims Management of familial hypercholesterolaemia (FH) may vary across
different settings due to factors related to population characteristics, practice, resources …

[HTML][HTML] Why patients with familial hypercholesterolemia are at high cardiovascular risk? Beyond LDL-C levels

V Bianconi, M Banach, M Pirro, ILE Panel - Trends in Cardiovascular …, 2021 - Elsevier
Familial hypercholesterolemia (FH) is a common genetic cause of elevated low-density
lipoprotein cholesterol (LDL-C) due to defective clearance of circulating LDL particles. All FH …

Familial hypercholesterolemia: A complex genetic disease with variable phenotypes

MD Di Taranto, C Giacobbe, G Fortunato - European journal of medical …, 2020 - Elsevier
Familial hypercholesterolemia (FH) is the most frequent genetic disease and is
characterized by elevation of LDL-cholesterol that accumulates in tissues leading to …

[HTML][HTML] Genetic heterogeneity of familial hypercholesterolemia: repercussions for molecular diagnosis

MD Di Taranto, G Fortunato - International Journal of Molecular Sciences, 2023 - mdpi.com
Genetics of Familial Hypercholesterolemia (FH) is ascribable to pathogenic variants in
genes encoding proteins leading to an impaired LDL uptake by the LDL receptor (LDLR) …

Single-pill fixed-dose drug combinations to reduce blood pressure: the right pill for the right patient

R Sarzani, G Laureti, A Gezzi… - … in Chronic Disease, 2022 - journals.sagepub.com
Arterial hypertension is one of the major causes of cardiovascular morbidity and mortality
worldwide. Effective and sustained reduction in blood pressure is essential to reduce …

[HTML][HTML] Regulation of cholesterol metabolism by bioactive components of soy proteins: Novel translational evidence

GR Caponio, DQH Wang, A Di Ciaula… - International Journal of …, 2020 - mdpi.com
Hypercholesterolemia represents one key pathophysiological factor predisposing to
increasing risk of developing cardiovascular disease worldwide. Controlling plasma …

Clinical implications of monogenic versus polygenic hypercholesterolemia: long‐term response to treatment, coronary atherosclerosis burden, and cardiovascular …

L D'Erasmo, I Minicocci, A Di Costanzo… - Journal of the …, 2021 - Am Heart Assoc
Background Familial hypercholesterolemia (FH) may arise from deleterious monogenic
variants in FH‐causing genes as well as from a polygenic cause. We evaluated the …

Platelet function and activation markers in primary hypercholesterolemia treated with anti-PCSK9 monoclonal antibody: A 12-month follow-up

C Barale, K Bonomo, C Frascaroli, A Morotti… - Nutrition, Metabolism …, 2020 - Elsevier
Background and aims In the association between hypercholesterolemia (HC) and
thrombotic risk platelet hyper-reactivity plays an important role. The inhibition of proprotein …