MAURIZIO MARGAGLIONE

Professore Ordinario

Università degli Studi di Foggia

Italy

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MAURIZIO MARGAGLIONE is a Professore Ordinario at Università degli Studi di Foggia, Italy. His research areas encompass clinical and genetic heterogeneity related to coagulation disorders, hereditary angioedema, genetic arrhythmias, and the implications of COVID-19 on various health outcomes. Recent publications highlight his contributions to understanding the genetic backgrounds of essential tremor and thrombosis as well as the psychosomatic aspects associated with heart failure.

Articles (13)

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2025

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2025

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2025

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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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2021

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2021

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2021

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2021

Collaborators (8)

Cristina Santoro

ITALY

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Francescopaolo Antonucci

ITALY

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Gilda Cinnella

Full Professor

University of Foggia

ITALY

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Maria D'APOLITO

Prof

University of Foggia

ITALY

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Elvira Grandone

University of Foggia

ITALY

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Fabrizio Gentile

Full Professor of General Pathology

University of Molise

ITALY

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Piero Porcelli

Full professor

University of Chieti-Pescara

ITALY

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Paul R.J. Ames

PORTUGAL

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MAURIZIO MARGAGLIONE

Research Interests

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Articles (13)

Clinical and Genetic Heterogeneity of Factor XI Deficiency: Insights from a Southern Italian Cohort

Vasculopathy: a possible factor affecting hereditary angioedema

Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study

A Novel <i>KCNN2</i> Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis

Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients

Earlier onset of peripheral arterial thrombosis in homozygous MTHFR C677T carriers than in other MTHFR genotypes: a cohort study

Increased SARS-CoV-2 seroprevalence in healthy blood donors after the second pandemic wave in South-Eastern Italy: evidence for asymptomatic young donors as potential virus spreaders

Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis

Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors

The Genetics of Hereditary Angioedema: A Review

Summary of the Available Molecular Methods for Detection of SARS-CoV-2 during the Ongoing Pandemic

Mortality and Transfusion Requirements in COVID-19 Hospitalized Italian Patients According to Severity of the Disease

Addressing the impact of SARS-CoV-2 infection in persons with congenital bleeding disorders: The Italian MECCOVID-19 study

Collaborators (8)

Cristina Santoro

Francescopaolo Antonucci

Gilda Cinnella

Maria D'APOLITO

Elvira Grandone

Fabrizio Gentile

Piero Porcelli

Paul R.J. Ames

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