Leccese, Angelica
Leccese, Angelica
Dipartimento di Medicina Clinica e Sperimentale
A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy
2024-01-01 Scioscia, Giulia; Santacroce, Rosa; Tondo, Pasquale; Hoxhallari, Anela; Soccio, Piera; Giuffreda, Ernesto; D'Ambrosio, Maria Francesca; Leccese, Angelica; Paladini, Luigi; Natale, Matteo Pio; Moriondo, Giorgia; Foschino Barbaro, Maria Pia; Margaglione, Maurizio; Lacedonia, Donato
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology
2024-01-01 D’Apolito, Maria; Santacroce, Rosa; Osvaldo Vazquez, Daniel; Cordisco, Giorgia; Agustin Fantini, Claudio; D’Andrea, Giovanna; Leccese, Angelica; Colia, ANNA LAURA; Martinez, Pablo; Zanichelli, Andrea; Josviack, Darıo; Margaglione, Maurizio
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU
2016-01-01 Trunzo, Roberta; Santacroce, Rosa; Shen, N; Jung Klawitter, S; Leccese, Angelica; DE GIROLAMO, Giuseppe; Margaglione, Maurizio; Blau, N.
Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’
2014-01-01 Trunzo, Roberta; Santacroce, Rosa; Leccese, Angelica; Pansini, A; Mattia, G; Margaglione, Maurizio
The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype
2015-01-01 Santacroce, Rosa; Trunzo, Roberta; Leccese, Angelica; Pansini, Angela; Gentile, Mattia; Margaglione, Maurizio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy | 1-gen-2024 | Scioscia, Giulia; Santacroce, Rosa; Tondo, Pasquale; Hoxhallari, Anela; Soccio, Piera; Giuffreda, Ernesto; D'Ambrosio, Maria Francesca; Leccese, Angelica; Paladini, Luigi; Natale, Matteo Pio; Moriondo, Giorgia; Foschino Barbaro, Maria Pia; Margaglione, Maurizio; Lacedonia, Donato | |
| DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology | 1-gen-2024 | D’Apolito, Maria; Santacroce, Rosa; Osvaldo Vazquez, Daniel; Cordisco, Giorgia; Agustin Fantini, Claudio; D’Andrea, Giovanna; Leccese, Angelica; Colia, ANNA LAURA; Martinez, Pablo; Zanichelli, Andrea; Josviack, Darıo; Margaglione, Maurizio | |
| In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU | 1-gen-2016 | Trunzo, Roberta; Santacroce, Rosa; Shen, N; Jung Klawitter, S; Leccese, Angelica; DE GIROLAMO, Giuseppe; Margaglione, Maurizio; Blau, N. | |
| Small Supernumerary Marker Chromosome Originating From Chromosome 10 Associated With an Apparently Normal Phenotype’ | 1-gen-2014 | Trunzo, Roberta; Santacroce, Rosa; Leccese, Angelica; Pansini, A; Mattia, G; Margaglione, Maurizio | |
| The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype | 1-gen-2015 | Santacroce, Rosa; Trunzo, Roberta; Leccese, Angelica; Pansini, Angela; Gentile, Mattia; Margaglione, Maurizio |