Works by De Luca, Alessandro

Results: 128
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    Biocycle between Design and Additive Manufacturing.

    Published in:
    Macromolecular Symposia, 2021, v. 396, n. 1, p. 1, doi. 10.1002/masy.202000313
    By:
    • Scognamiglio, Ciro;
    • Capece, Sonia;
    • De Luca, Alessandro;
    • Amendola, Eugenio;
    • Egido‐Villarreal, Janitzio;
    • Buono, Mario
    Publication type:
    Article
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    Stabilization of an underactuated planar 2R manipulator.

    Published in:
    International Journal of Robust & Nonlinear Control, 2000, v. 10, n. 4, p. 181, doi. 10.1002/(SICI)1099-1239(20000415)10:4<181::AID-RNC471>3.0.CO;2-X
    By:
    • De Luca, Alessandro;
    • Mattone, Raffaella;
    • Oriolo, Giuseppe
    Publication type:
    Article
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    Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co‐inheritance.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1336
    By:
    • Traversa, Alice;
    • Marchionni, Enrica;
    • Giovannetti, Agnese;
    • Genovesi, Maria L.;
    • Panzironi, Noemi;
    • Margiotti, Katia;
    • Napoli, Giulia;
    • Piceci Sparascio, Francesca;
    • De Luca, Alessandro;
    • Petrizzelli, Francesco;
    • Carella, Massimo;
    • Cardona, Francesco;
    • Bernardo, Silvia;
    • Manganaro, Lucia;
    • Mazza, Tommaso;
    • Pizzuti, Antonio;
    • Caputo, Viviana
    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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    Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis‐van Creveld syndrome caused by hypomorphic mutations in the EVC gene.

    Published in:
    Human Mutation, 2020, v. 41, n. 12, p. 2087, doi. 10.1002/humu.24112
    By:
    • Piceci‐Sparascio, Francesca;
    • Palencia‐Campos, Adrian;
    • Soto‐Bielicka, Patricia;
    • D'Anzi, Angela;
    • Guida, Valentina;
    • Rosati, Jessica;
    • Caparros‐Martin, Jose A.;
    • Torrente, Isabella;
    • D'Asdia, M. Cecilia;
    • Versacci, Paolo;
    • Briuglia, Silvana;
    • Lapunzina, Pablo;
    • Tartaglia, Marco;
    • Marino, Bruno;
    • Digilio, M. Cristina;
    • Ruiz‐Perez, Victor L.;
    • 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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    Transplantation of clinical-grade human neural stem cells reduces neuroinflammation, prolongs survival and delays disease progression in the SOD1 rats.

    Published in:
    Cell Death & Disease, 2019, v. 10, n. 5, p. N.PAG, doi. 10.1038/s41419-019-1582-5
    By:
    • Zalfa, Cristina;
    • Rota Nodari, Laura;
    • Vacchi, Elena;
    • Gelati, Maurizio;
    • Profico, Daniela;
    • Boido, Marina;
    • Binda, Elena;
    • De Filippis, Lidia;
    • Copetti, Massimiliano;
    • Garlatti, Valentina;
    • Daniele, Paola;
    • Rosati, Jessica;
    • De Luca, Alessandro;
    • Pinos, Francesca;
    • Cajola, Laura;
    • Visioli, Alberto;
    • Mazzini, Letizia;
    • Vercelli, Alessandro;
    • Svelto, Maria;
    • Vescovi, Angelo Luigi
    Publication type:
    Article
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    Algorithm of rational approach to reconstruction in Fournier’s disease.

    Published in:
    Open Medicine, 2021, v. 16, n. 1, p. 1028, doi. 10.1515/med-2021-0294
    By:
    • Tripodi, Domenico;
    • Amabile, Maria Ida;
    • Gagliardi, Federica;
    • Frusone, Federico;
    • Varanese, Marzia;
    • De Luca, Alessandro;
    • Pironi, Daniele;
    • D’ Andrea, Vito;
    • Sorrenti, Salvatore;
    • Cannistrà, Claudio
    Publication type:
    Article
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    Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 13, p. 2133, doi. 10.1093/hmg/ddz046
    By:
    • Fusco, Carmela;
    • Nardella, Grazia;
    • Fischetto, Rita;
    • Copetti, Massimiliano;
    • Petracca, Antonio;
    • Annunziata, Francesca;
    • Augello, Bartolomeo;
    • D'Asdia, Maria Cecilia;
    • Petrucci, Simona;
    • Mattina, Teresa;
    • Rella, Annalisa;
    • Cassina, Matteo;
    • Bengala, Mario;
    • Biagini, Tommaso;
    • Causio, Francesco Andrea;
    • Caldarini, Camilla;
    • Brancati, Francesco;
    • Luca, Alessandro De;
    • Guarnieri, Vito;
    • Micale, Lucia
    Publication type:
    Article
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