Angelica Leccese

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

Valeria Bafunno, Davide Firinu, Maria D’Apolito et al. · Journal of Allergy and Clinical Immunology · 2017 · 304 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

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

Maria D’Apolito, Rosa Santacroce, Daniel Vázquez et al. · Journal of Allergy and Clinical Immunology · 2024 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

Roberta Trunzo, Rosa Santacroce, Giovanna D’Andrea et al. · Clinica Chimica Acta · 2015 · 28 citations

Life Sciences, Genetics, Molecular Genetics +16

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

Roberta Trunzo, Rosa Santacroce, Nan Shen et al. · Gene · 2016 · 18 citations

Life Sciences, Biochemistry, Molecular Genetics +14

Mutation analysis in hyperphenylalaninemia patients from South Italy

Roberta Trunzo, Rosa Santacroce, Giovanna D’Andrea et al. · Clinical Biochemistry · 2013 · 15 citations

Life Sciences, Genetics, Molecular Genetics +14