Giorgia Cordisco

Foggia, Italy

Last Updated: 09/26/2026

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Found 10 publications

Incidental findings of inherited thrombosis and hemostasis disorders in clinical exomes with unrelated indications.

Incidental findings of inherited thrombosis and hemostasis disorders in clinical exomes with unrelated indications.

Journal: Haematologica

Published: June 10, 2026

Unveiling Rare Genetic Variants in DAB2IP: New Insights Into the Pathogenesis of Recurrent Angioedema.

Unveiling Rare Genetic Variants in DAB2IP: New Insights Into the Pathogenesis of Recurrent Angioedema.

Journal: Allergy

Published: September 24, 2025

DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology.

DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology.

Journal: The Journal of allergy and clinical immunology

Published: January 21, 2024

A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis.

A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis.

Journal: Genes

Published: January 14, 2023

Angiotensin-Converting Enzyme Inhibitor-Associated Angioedema: From Bed to Bench.

Angiotensin-Converting Enzyme Inhibitor-Associated Angioedema: From Bed to Bench.

Journal: Journal of investigational allergology & clinical immunology

Published: October 11, 2019

Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor.

Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor.

Journal: Allergy

Published: July 04, 2019

Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes.

Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes.

Journal: Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing

Published: March 22, 2019

Double de novo mutations in dilated cardiomyopathy with cardiac arrest.

Double de novo mutations in dilated cardiomyopathy with cardiac arrest.

Journal: Journal of electrocardiology

Published: October 13, 2018

Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema.

Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: May 22, 2018

Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema.

Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema.

Journal: The Journal of allergy and clinical immunology

Published: February 22, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026