Sebastiano Calandra

Emeritus Professor of General Pathology

University of Modena and Reggio Emilia

Italy

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About

Sebastiano Calandra is an Emeritus Professor of General Pathology at the University of Modena and Reggio Emilia, Italy. His research primarily focuses on familial hypercholesterolemia, particularly in pediatric populations, as demonstrated by his recent publications. Calandra has investigated various aspects including clinical management, genetic characterization, and risk stratification related to lipid disorders. His contributions aim to enhance the understanding and treatment of cholesterol-related conditions in children and adolescents.

Articles (12)

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2020

Collaborators (15)

Giuseppe Mandraffino

Senior Assistant Professor

University of Messina

ITALY

Sebastiano Calandra

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Articles (12)

Identification and Molecular Characterization of a Novel Large-Scale Variant (Exons 4_18 Loss) in the LDLR Gene as a Cause of Familial Hypercholesterolaemia in an Italian Family

Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric Group

Functional Characterization of p.(Arg160Gln) PCSK9 Variant Accidentally Found in a Hypercholesterolemic Subject

Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study.

Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia.

Plasma HDL pattern, cholesterol efflux and cholesterol loading capacity of serum in carriers of a novel missense variant (Gly176Trp) of endothelial lipase.

Lipoprotein(a) and family history for cardiovascular disease in paediatric patients: A new frontier in cardiovascular risk stratification. Data from the LIPIGEN paediatric group.

Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations.

Search for familial hypercholesterolemia patients in an Italian community: A real-life retrospective study.

Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study.

The Role of Registers in Increasing Knowledge and Improving Management of Children and Adolescents Affected by Familial Hypercholesterolemia: the LIPIGEN Pediatric Group.

Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features.

Collaborators (15)

Giuseppe Mandraffino

Manuela Casula

Livia Pisciotta

Angelina Passaro

Maria Del Ben

MARCO BUCCI

Angelo Minucci

concetta santonocito

cesar martin

Simonetta Genovesi

Martina Rinelli

Lorenzo Iughetti

Patrizia Tarugi

Roberto Scicali

Paolo Calabrò

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