Search Results - Dallapiccola, Matteo

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  1. 1
    Wheelchair driving strategies: A comparison between standard joystick and gaze-based control

    Wheelchair driving strategies: A comparison between standard joystick and gaze-based control by Maule, Luca, Zanetti, Matteo, Luchetti, Alessandro, Tomasin, Paolo, Dallapiccola, Matteo, Covre, Nicola, Guandalini, Giovanni, De Cecco, Mariolino

    Published in Assistive technology
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  2. 2
    Machine learning as a surrogate model for EnergyPLAN: Speeding up energy system optimization at the country level

    Machine learning as a surrogate model for EnergyPLAN: Speeding up energy system optimization at the country level by Prina, Matteo Giacomo, Dallapiccola, Mattia, Moser, David, Sparber, Wolfram

    Published in Energy (Oxford)
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  3. 3
    Analysis of gut microbiota in patients with Williams–Beuren Syndrome reveals dysbiosis linked to clinical manifestations

    Analysis of gut microbiota in patients with Williams–Beuren Syndrome reveals dysbiosis linked to clinical manifestations by Del Chierico, Federica, Marzano, Valeria, Scanu, Matteo, Reddel, Sofia, Dentici, Maria Lisa, Capolino, Rossella, Di Donato, Maddalena, Spasari, Iolanda, Fiscarelli, Ersilia Vita, Digilio, Maria Cristina, Abreu, Maria Teresa, Dallapiccola, Bruno, Putignani, Lorenza

    Published in Scientific reports
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  4. 4
    Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients

    Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients by Micale, Lucia, Augello, Bartolomeo, Fusco, Carmela, Selicorni, Angelo, Loviglio, Maria N, Silengo, Margherita Cirillo, Reymond, Alexandre, Gumiero, Barbara, Zucchetti, Federica, D'Addetta, Ester V, Belligni, Elga, Calcagnì, Alessia, Digilio, Maria C, Dallapiccola, Bruno, Faravelli, Francesca, Forzano, Francesca, Accadia, Maria, Bonfante, Aldo, Clementi, Maurizio, Daolio, Cecilia, Douzgou, Sofia, Ferrari, Paola, Fischetto, Rita, Garavelli, Livia, Lapi, Elisabetta, Mattina, Teresa, Melis, Daniela, Patricelli, Maria G, Priolo, Manuela, Prontera, Paolo, Renieri, Alessandra, Mencarelli, Maria A, Scarano, Gioacchino, della Monica, Matteo, Toschi, Benedetta, Turolla, Licia, Vancini, Alessandra, Zatterale, Adriana, Gabrielli, Orazio, Zelante, Leopoldo, Merla, Giuseppe

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  5. 5
    Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disorders

    Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disorders by Smith, Michael, Alexander, Elizabeth, Marcinkute, Ruta, Dan, Dorica, Rawson, Myfanwy, Banka, Siddharth, Gavin, Jason, Mina, Hany, Hennessy, Con, Riccardi, Florence, Radio, Francesca Clementina, Havlovicova, Marketa, Cassina, Matteo, Emandi, Adela Chirita, Fradin, Melanie, Gompertz, Lianne, Nordgren, Ann, Traberg, Rasa, Rossi, Massimiliano, Trimouille, Aurelién, Sowmyalakshmi, Rasika, Dallapiccola, Bruno, Renieri, Alessandra, Faivre, Laurence, Kerr, Bronwyn, Verloes, Alain, Clayton-Smith, Jill, Douzgou, Sofia

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  6. 6
    Small 4p16.3 deletions: Three additional patients and review of the literature

    Small 4p16.3 deletions: Three additional patients and review of the literature by Bernardini, Laura, Radio, Francesca C., Acquaviva, Fabio, Gorgone, Cristina, Postorivo, Diana, Torres, Barbara, Alesi, Viola, Magliozzi, Monia, Lonardo, Fortunato, Monica, Matteo Della, Nardone, Anna M., Cesario, Claudia, Mattina, Teresa, Scarano, Gioacchino, Dallapiccola, Bruno, Digilio, Maria C., Novelli, Antonio

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  7. 7
    Kinematic and diffusion tensor imaging definition of familial Marcus Gunn jaw-winking synkinesis

    Kinematic and diffusion tensor imaging definition of familial Marcus Gunn jaw-winking synkinesis by Conte, Antonella, Brancati, Francesco, Garaci, Francesco, Toschi, Nicola, Bologna, Matteo, Fabbrini, Giovanni, Falla, Marika, Dallapiccola, Bruno, Bollero, Patrizio, Floris, Roberto, Berardelli, Alfredo

    Published in PloS one
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  8. 8
    A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign

    A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign by Restaldi, Fabrizia, Alesi, Viola, Aquilani, Angela, Genovese, Silvia, Russo, Serena, Coletti, Valentina, Pompili, Daniele, Falasca, Roberto, Dallapiccola, Bruno, Capolino, Rossella, Luciani, Matteo, Novelli, Antonio

    Published in Molecular cytogenetics
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  9. 9
    SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers

    SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers by Guglielmi, Valeria, Vattemi, Gaetano, Gualandi, Francesca, Voermans, Nicol C., Marini, Matteo, Scotton, Chiara, Pegoraro, Elena, Oosterhof, Arie, Kósa, Magdolna, Zádor, Ernő, Valente, Enza Maria, De Grandis, Domenico, Neri, Marcella, Codemo, Valentina, Novelli, Antonio, van Kuppevelt, Toin H., Dallapiccola, Bruno, van Engelen, Baziel G., Ferlini, Alessandra, Tomelleri, Giuliano

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  10. 10
    A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign

    A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign by Restaldi, Fabrizia, Alesi, Viola, Aquilani, Angela, Genovese, Silvia, Russo, Serena, Coletti, Valentina, Pompili, Daniele, Falasca, Roberto, Dallapiccola, Bruno, Capolino, Rossella, Luciani, Matteo, Novelli, Antonio

    Published in Molecular cytogenetics
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