Angelica Leccese

Foggia, Italy

Last Updated: 09/26/2026

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Found 15 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

A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy.

A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy.

Journal: Archivos de bronconeumologia

Published: February 07, 2024

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

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

Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria.

Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria.

Journal: BMC pregnancy and childbirth

Published: May 27, 2018

A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis.

A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis.

Journal: Lung

Published: March 20, 2017

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

In vitro residual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU.

In vitro residual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU.

Journal: Gene

Published: July 05, 2016

The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype.

The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype.

Journal: Systems biology in reproductive medicine

Published: August 14, 2015

Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.

Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: May 28, 2015

Identification of ten novel mutations in factor VIII gene: A study of a cohort of 52 haemophilia A patients.

Identification of ten novel mutations in factor VIII gene: A study of a cohort of 52 haemophilia A patients.

Journal: Thrombosis research

Published: December 02, 2014

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Last Updated: 09/26/2026