Works by De Luca, Alessandro


Results: 130
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    Intracholecystic versus Intravenous Indocyanine Green (ICG) Injection for Biliary Anatomy Evaluation by Fluorescent Cholangiography during Laparoscopic Cholecystectomy: A Case–Control Study.

    Published in:
    Journal of Clinical Medicine, 2022, v. 11, n. 12, p. 3508, doi. 10.3390/jcm11123508
    By:
    • Castagneto-Gissey, Lidia;
    • Russo, Maria Francesca;
    • Iodice, Alessandra;
    • Casella-Mariolo, James;
    • Serao, Angelo;
    • Picchetto, Andrea;
    • D'Ambrosio, Giancarlo;
    • Urciuoli, Irene;
    • De Luca, Alessandro;
    • Salvati, Bruno;
    • Casella, Giovanni
    Publication type:
    Article
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    Further case of enlarged spinal nerve roots in KRAS‐related Noonan syndrome.

    Published in:
    Clinical Genetics, 2023, v. 104, n. 1, p. 136, doi. 10.1111/cge.14308
    By:
    • Leoni, Chiara;
    • Viscogliosi, Germana;
    • Onesimo, Roberta;
    • Verdolotti, Tommaso;
    • Biagini, Tommaso;
    • Mazza, Tommaso;
    • De Luca, Alessandro;
    • Perri, Lucrezia;
    • Trevisan, Valentina;
    • Flex, Elisabetta;
    • Tartaglia, Marco;
    • Zampino, Giuseppe
    Publication type:
    Article
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    Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 5, p. 563, doi. 10.1111/cge.14040
    By:
    • D'Amico, Alessandra;
    • Rosano, Carmen;
    • Pannone, Luca;
    • Pinna, Valentina;
    • Assunto, Antonia;
    • Motta, Marialetizia;
    • Ugga, Lorenzo;
    • Daniele, Paola;
    • Mandile, Roberta;
    • Mariniello, Lucio;
    • Siano, Maria Anna;
    • Santoro, Claudia;
    • Piluso, Giulio;
    • Martinelli, Simone;
    • Strisciuglio, Pietro;
    • De Luca, Alessandro;
    • Tartaglia, Marco;
    • Melis, Daniela
    Publication type:
    Article
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    A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 1, p. 69, doi. 10.1038/ejhg.2012.109
    By:
    • Guida, Valentina;
    • Ferese, Rosangela;
    • Rocchetti, Marcella;
    • Bonetti, Monica;
    • Sarkozy, Anna;
    • Cecchetti, Serena;
    • Gelmetti, Vania;
    • Lepri, Francesca;
    • Copetti, Massimiliano;
    • Lamorte, Giuseppe;
    • Cristina Digilio, Maria;
    • Marino, Bruno;
    • Zaza, Antonio;
    • den Hertog, Jeroen;
    • Dallapiccola, Bruno;
    • De Luca, Alessandro
    Publication type:
    Article
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    "Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats.

    Published in:
    Journal of Personalized Medicine, 2022, v. 12, n. 1, p. 120, doi. 10.3390/jpm12010120
    By:
    • Graziola, Federica;
    • Maffi, Sabrina;
    • Grasso, Melissa;
    • Garone, Giacomo;
    • Migliore, Simone;
    • Scaricamazza, Eugenia;
    • Ceccarelli, Consuelo;
    • Casella, Melissa;
    • Busi, Ludovica;
    • D'Alessio, Barbara;
    • De Luca, Alessandro;
    • Colafati, Giovanna Stefania;
    • Sabatini, Umberto;
    • Capuano, Alessandro;
    • Squitieri, Ferdinando
    Publication type:
    Article
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    Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.

    Published in:
    Genes, 2021, v. 12, n. 7, p. 1047, doi. 10.3390/genes12071047
    By:
    • Calcagni, Giulio;
    • Pugnaloni, Flaminia;
    • Digilio, Maria Cristina;
    • Unolt, Marta;
    • Putotto, Carolina;
    • Niceta, Marcello;
    • Baban, Anwar;
    • Piceci Sparascio, Francesca;
    • Drago, Fabrizio;
    • De Luca, Alessandro;
    • Tartaglia, Marco;
    • Marino, Bruno;
    • Versacci, Paolo
    Publication type:
    Article
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    DNA Methylation in the Diagnosis of Monogenic Diseases.

    Published in:
    Genes, 2020, v. 11, n. 4, p. 355, doi. 10.3390/genes11040355
    By:
    • Cerrato, Flavia;
    • Sparago, Angela;
    • Ariani, Francesca;
    • Brugnoletti, Fulvia;
    • Calzari, Luciano;
    • Coppedè, Fabio;
    • De Luca, Alessandro;
    • Gervasini, Cristina;
    • Giardina, Emiliano;
    • Gurrieri, Fiorella;
    • Lo Nigro, Cristiana;
    • Merla, Giuseppe;
    • Miozzo, Monica;
    • Russo, Silvia;
    • Sangiorgi, Eugenio;
    • Sirchia, Silvia M;
    • Squeo, Gabriella Maria;
    • Tabano, Silvia;
    • Tabolacci, Elisabetta;
    • Torrente, Isabella
    Publication type:
    Article
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    Founder and Recurrent CDH1 Mutations in Families With Hereditary Diffuse Gastric Cancer.

    Published in:
    JAMA: Journal of the American Medical Association, 2007, v. 297, n. 21, p. 2360, doi. 10.1001/jama.297.21.2360
    By:
    • Kaurah, Pardeep;
    • MacMillan, Andrée;
    • Boyd, Niki;
    • Senz, Janine;
    • De Luca, Alessandro;
    • Chun, Nicki;
    • Suriano, Gianpaolo;
    • Zaor, Sunya;
    • Van Manen, Lori;
    • Gilpin, Cathy;
    • Nikkel, Sarah;
    • Connolly-Wilson, Mary;
    • Weissman, Scott;
    • Rubinstein, Wendy S.;
    • Sebold, Courtney;
    • Greenstein, Robert;
    • Stroop, Jennifer;
    • Yim, Dwight;
    • Panzini, Benoit;
    • McKinnon, Wendy
    Publication type:
    Article
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