Works by Tartaglia, Marco

Results: 210
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    Neurobehavioral features in individuals with Kabuki syndrome.

    Published in:
    Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 3, p. 322, doi. 10.1002/mgg3.348
    By:
    • Caciolo, Cristina;
    • Alfieri, Paolo;
    • Piccini, Giorgia;
    • Digilio, Maria Cristina;
    • Lepri, Francesca Romana;
    • Tartaglia, Marco;
    • Menghini, Deny;
    • Vicari, Stefano
    Publication type:
    Article
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    Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37585-8
    By:
    • Melo, Uirá Souto;
    • Jatzlau, Jerome;
    • Prada-Medina, Cesar A.;
    • Flex, Elisabetta;
    • Hartmann, Sunhild;
    • Ali, Salaheddine;
    • Schöpflin, Robert;
    • Bernardini, Laura;
    • Ciolfi, Andrea;
    • Moeinzadeh, M-Hossein;
    • Klever, Marius-Konstantin;
    • Altay, Aybuge;
    • Vallecillo-García, Pedro;
    • Carpentieri, Giovanna;
    • Delledonne, Massimo;
    • Ort, Melanie-Jasmin;
    • Schwestka, Marko;
    • Ferrero, Giovanni Battista;
    • Tartaglia, Marco;
    • Brusco, Alfredo
    Publication type:
    Article
    9

    Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation.

    Published in:
    2023
    By:
    • Melo, Uirá Souto;
    • Jatzlau, Jerome;
    • Prada-Medina, Cesar A.;
    • Flex, Elisabetta;
    • Hartmann, Sunhild;
    • Ali, Salaheddine;
    • Schöpflin, Robert;
    • Bernardini, Laura;
    • Ciolfi, Andrea;
    • Moeinzadeh, M-Hossein;
    • Klever, Marius-Konstantin;
    • Altay, Aybuge;
    • Vallecillo-García, Pedro;
    • Carpentieri, Giovanna;
    • Delledonne, Massimo;
    • Ort, Melanie-Jasmin;
    • Schwestka, Marko;
    • Ferrero, Giovanni Battista;
    • Tartaglia, Marco;
    • Brusco, Alfredo
    Publication type:
    Correction Notice
    10

    Melanotic Neuroectodermal Tumor of Infancy (MNTI) and Pineal Anlage Tumor (PAT) Harbor A Medulloblastoma Signature by DNA Methylation Profiling.

    Published in:
    Cancers, 2021, v. 13, n. 4, p. 706, doi. 10.3390/cancers13040706
    By:
    • Lopez-Nunez, Oscar;
    • Alaggio, Rita;
    • John, Ivy;
    • Ciolfi, Andrea;
    • Pedace, Lucia;
    • Mastronuzzi, Angela;
    • Gianno, Francesca;
    • Giangaspero, Felice;
    • Rossi, Sabrina;
    • Donofrio, Vittoria;
    • Cinalli, Giuseppe;
    • Surrey, Lea F.;
    • Tartaglia, Marco;
    • Locatelli, Franco;
    • Miele, Evelina;
    • Singh, Sheila K.
    Publication type:
    Article
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    The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans.

    Published in:
    Frontiers in Molecular Neuroscience, 2023, p. 1, doi. 10.3389/fnmol.2023.1170061
    By:
    • Pannone, Luca;
    • Muto, Valentina;
    • Nardecchia, Francesca;
    • Di Rocco, Martina;
    • Marchei, Emilia;
    • Tosato, Federica;
    • Petrini, Stefania;
    • Onorato, Giada;
    • Lanza, Enrico;
    • Bertuccini, Lucia;
    • Manti, Filippo;
    • Folli, Viola;
    • Galosi, Serena;
    • Di Schiavi, Elia;
    • Leuzzi, Vincenzo;
    • Tartaglia, Marco;
    • Martinelli, Simone
    Publication type:
    Article
    14

    Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations.

    Published in:
    2017
    By:
    • Nasca, Alessia;
    • Rizza, Teresa;
    • Doimo, Mara;
    • Legati, Andrea;
    • Ciolfi, Andrea;
    • Diodato, Daria;
    • Calderan, Cristina;
    • Carrara, Gianfranco;
    • Lamantea, Eleonora;
    • Aiello, Chiara;
    • Di Nottia, Michela;
    • Niceta, Marcello;
    • Lamperti, Costanza;
    • Ardissone, Anna;
    • Bianchi-Marzoli, Stefania;
    • Iarossi, Giancarlo;
    • Bertini, Enrico;
    • Moroni, Isabella;
    • Tartaglia, Marco;
    • Salviati, Leonardo
    Publication type:
    journal article
    15

    Expanding the spectrum of EWSR1‐PATZ1 rearranged CNS tumors: An infantile case with leptomeningeal dissemination.

    Published in:
    Brain Pathology, 2021, v. 31, n. 3, p. 1, doi. 10.1111/bpa.12934
    By:
    • Rossi, Sabrina;
    • Barresi, Sabina;
    • Giovannoni, Isabella;
    • Alesi, Viola;
    • Ciolfi, Andrea;
    • Colafati, Giovanna Stefania;
    • Diomedi‐Camassei, Francesca;
    • Miele, Evelina;
    • Cacchione, Antonella;
    • Quacquarini, Denise;
    • Carai, Andrea;
    • Tartaglia, Marco;
    • Giannini, Caterina;
    • Giangaspero, Felice;
    • Mastronuzzi, Angela;
    • Alaggio, Rita
    Publication type:
    Article
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    RAF1 gene fusions are recurrent driver events in infantile fibrosarcoma‐like mesenchymal tumors.

    Published in:
    Journal of Pathology, 2024, v. 263, n. 2, p. 166, doi. 10.1002/path.6272
    By:
    • Motta, Marialetizia;
    • Barresi, Sabina;
    • Pizzi, Simone;
    • Bifano, Delfina;
    • Lopez Marti, Jennifer;
    • Garrido‐Pontnou, Marta;
    • Flex, Elisabetta;
    • Bruselles, Alessandro;
    • Giovannoni, Isabella;
    • Rotundo, Giovannina;
    • Fragale, Alessandra;
    • Tirelli, Valentina;
    • Vallese, Silvia;
    • Ciolfi, Andrea;
    • Bisogno, Gianni;
    • Alaggio, Rita;
    • Tartaglia, Marco
    Publication type:
    Article
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    Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiency.

    Published in:
    Journal of Inherited Metabolic Disease, 2016, v. 39, n. 5, p. 689, doi. 10.1007/s10545-016-9956-7
    By:
    • Dionisi-Vici, Carlo;
    • Shteyer, Eyal;
    • Niceta, Marcello;
    • Rizzo, Cristiano;
    • Pode-Shakked, Ben;
    • Chillemi, Giovanni;
    • Bruselles, Alessandro;
    • Semeraro, Michela;
    • Barel, Ortal;
    • Eyal, Eran;
    • Kol, Nitzan;
    • Haberman, Yael;
    • Lahad, Avishai;
    • Diomedi-Camassei, Francesca;
    • Marek-Yagel, Dina;
    • Rechavi, Gideon;
    • Tartaglia, Marco;
    • Anikster, Yair
    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
    21

    Pathogenic PTPN11 variants involving the poly‐glutamine Gln<sup>255</sup>‐Gln<sup>256</sup>‐Gln<sup>257</sup> stretch highlight the relevance of helix B in SHP2's functional regulation.

    Published in:
    Human Mutation, 2020, v. 41, n. 6, p. 1171, doi. 10.1002/humu.24007
    By:
    • Martinelli, Simone;
    • Pannone, Luca;
    • Lissewski, Christina;
    • Brinkmann, Julia;
    • Flex, Elisabetta;
    • Schanze, Denny;
    • Calligari, Paolo;
    • Anselmi, Massimiliano;
    • Pantaleoni, Francesca;
    • Canale, Viviana Claudia;
    • Radio, Francesca Clementina;
    • Ioannides, Adonis;
    • Rahner, Nils;
    • Schanze, Ina;
    • Josifova, Dragana;
    • Bocchinfuso, Gianfranco;
    • Ryten, Mina;
    • Stella, Lorenzo;
    • Tartaglia, Marco;
    • Zenker, Martin
    Publication type:
    Article
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    Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature.

    Published in:
    Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-019-0804-0
    By:
    • Ciolfi, Andrea;
    • Aref-Eshghi, Erfan;
    • Pizzi, Simone;
    • Pedace, Lucia;
    • Miele, Evelina;
    • Kerkhof, Jennifer;
    • Flex, Elisabetta;
    • Martinelli, Simone;
    • Radio, Francesca Clementina;
    • Ruivenkamp, Claudia A. L.;
    • Santen, Gijs W. E.;
    • Bijlsma, Emilia;
    • Barge-Schaapveld, Daniela;
    • Ounap, Katrin;
    • Siu, Victoria Mok;
    • Kooy, R. Frank;
    • Dallapiccola, Bruno;
    • Sadikovic, Bekim;
    • Tartaglia, Marco
    Publication type:
    Article
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    Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome.

    Published in:
    Movement Disorders, 2024, v. 39, n. 7, p. 1225, doi. 10.1002/mds.29795
    By:
    • Galosi, Serena;
    • Mancini, Cecilia;
    • Commone, Anna;
    • Calligari, Paolo;
    • Caputo, Viviana;
    • Nardecchia, Francesca;
    • Carducci, Claudia;
    • van den Heuvel, Lambertus P.;
    • Pizzi, Simone;
    • Bruselles, Alessandro;
    • Niceta, Marcello;
    • Martinelli, Simone;
    • Rodenburg, Richard J.;
    • Tartaglia, Marco;
    • Leuzzi, Vincenzo
    Publication type:
    Article
    29

    Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome.

    Published in:
    Nature, 2010, v. 465, n. 7299, p. 808, doi. 10.1038/nature09005
    By:
    • Carvajal-Vergara, Xonia;
    • Sevilla, Ana;
    • D'Souza, Sunita L.;
    • Ang, Yen-Sin;
    • Schaniel, Christoph;
    • Lee, Dung-Fang;
    • Lei Yang;
    • Kaplan, Aaron D.;
    • Adler, Eric D.;
    • Rozov, Roye;
    • YongChao Ge;
    • Cohen, Ninette;
    • Edelmann, Lisa J.;
    • Chang, Betty;
    • Waghray, Avinash;
    • Jie Su;
    • Pardo, Sherly;
    • Lichtenbelt, Klaske D.;
    • Tartaglia, Marco;
    • Gelb, Bruce D.
    Publication type:
    Article
    30

    Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.

    Published in:
    Human Genetics, 2002, v. 111, n. 4/5, p. 421, doi. 10.1007/s00439-002-0803-6
    By:
    • Ion, Andra;
    • Tartaglia, Marco;
    • Song, Xiaoling;
    • Kalidas, Kamini;
    • van der Burgt, Ineke;
    • Shaw, Adam C.;
    • Ming, Jeffrey E.;
    • Zampino, Giuseppe;
    • Zackai, Elaine H.;
    • Dean, John C.;
    • Somer, Mirja;
    • Parenti, Giancarlo;
    • Crosby, Andrew H.;
    • Patton, Michael A.;
    • Gelb, Bruce D.;
    • Jeffery, Steve
    Publication type:
    Article
    31

    Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy.

    Published in:
    Human Molecular Genetics, 2020, v. 29, n. 11, p. 1772, doi. 10.1093/hmg/ddz108
    By:
    • Motta, Marialetizia;
    • Sagi-Dain, Lena;
    • Krumbach, Oliver H F;
    • Hahn, Andreas;
    • Peleg, Amir;
    • German, Alina;
    • Lissewski, Christina;
    • Coppola, Simona;
    • Pantaleoni, Francesca;
    • Kocherscheid, Luisa;
    • Altmüller, Franziska;
    • Schanze, Denny;
    • Logeswaran, Thushiha;
    • Chahrokh-Zadeh, Soheyla;
    • Munzig, Anna;
    • Nakhaei-Rad, Saeideh;
    • Cavé, Hélène;
    • Ahmadian, Mohammad R;
    • Tartaglia, Marco;
    • Zenker, Martin
    Publication type:
    Article
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    Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 11, p. 1892, doi. 10.1093/hmg/ddy096
    By:
    • Sferra, Antonella;
    • Fattori, Fabiana;
    • Rizza, Teresa;
    • Flex, Elsabetta;
    • Bellacchio, Emanuele;
    • Bruselles, Alessandro;
    • Petrini, Stefania;
    • Cecchetti, Serena;
    • Teson, Massimo;
    • Restaldi, Fabrizia;
    • Ciolfi, Andrea;
    • Santorelli, Filippo M.;
    • Zanni, Ginevra;
    • Barresi, Sabina;
    • Castiglioni, Claudia;
    • Tartaglia, Marco;
    • Bertini, Enrico
    Publication type:
    Article
    34

    Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-54294-y
    By:
    • Iannuzzo, Alberto;
    • Delafontaine, Selket;
    • El Masri, Rana;
    • Tacine, Rachida;
    • Prencipe, Giusi;
    • Nishitani-Isa, Masahiko;
    • van Wijck, Rogier T. A.;
    • Bhuyan, Farzana;
    • de Jesus Rasheed, Adriana A.;
    • Coppola, Simona;
    • van Daele, Paul L. A.;
    • Insalaco, Antonella;
    • Goldbach-Mansky, Raphaela;
    • Yasumi, Takahiro;
    • Tartaglia, Marco;
    • Meyts, Isabelle;
    • Delon, Jérôme
    Publication type:
    Article
    35

    Correction to: Focal adhesion kinase inhibitor TAE226 combined with Sorafenib slows down hepatocellular carcinoma by multiple epigenetic effects.

    Published in:
    2022
    By:
    • Romito, Ilaria;
    • Porru, Manuela;
    • Braghini, Maria Rita;
    • Pompili, Luca;
    • Panera, Nadia;
    • Crudele, Annalisa;
    • Gnani, Daniela;
    • De Stefanis, Cristiano;
    • Scarsella, Marco;
    • Pomella, Silvia;
    • Mortera, Stefano Levi;
    • de Billy, Emmanuel;
    • Conti, Adrian Libenzio;
    • Marzano, Valeria;
    • Putignani, Lorenza;
    • Vinciguerra, Manlio;
    • Balsano, Clara;
    • Pastore, Anna;
    • Rota, Rossella;
    • Tartaglia, Marco
    Publication type:
    Correction Notice
    36

    Focal adhesion kinase inhibitor TAE226 combined with Sorafenib slows down hepatocellular carcinoma by multiple epigenetic effects.

    Published in:
    Journal of Experimental & Clinical Cancer Research (17569966), 2021, v. 40, n. 1, p. 1, doi. 10.1186/s13046-021-02154-8
    By:
    • Romito, Ilaria;
    • Porru, Manuela;
    • Braghini, Maria Rita;
    • Pompili, Luca;
    • Panera, Nadia;
    • Crudele, Annalisa;
    • Gnani, Daniela;
    • De Stefanis, Cristiano;
    • Scarsella, Marco;
    • Pomella, Silvia;
    • Levi Mortera, Stefano;
    • de Billy, Emmanuel;
    • Conti, Adrian Libenzio;
    • Marzano, Valeria;
    • Putignani, Lorenza;
    • Vinciguerra, Manlio;
    • Balsano, Clara;
    • Pastore, Anna;
    • Rota, Rossella;
    • Tartaglia, Marco
    Publication type:
    Article
    37

    Corrigendum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

    Published in:
    2007
    By:
    • Tartaglia, Marco;
    • Pennacchio, Len A;
    • Zhao, Chen;
    • Yadav, Kamlesh K;
    • Fodale, Valentina;
    • Sarkozy, Anna;
    • Pandit, Bhaswati;
    • Oishi, Kimihiko;
    • Martinelli, Simone;
    • Schackwitz, Wendy;
    • Ustaszewska, Anna;
    • Martin, Joel;
    • Bristow, James;
    • Carta, Claudio;
    • Lepri, Francesca;
    • Neri, Cinzia;
    • Vasta, Isabella;
    • Gibson, Kate;
    • Curry, Cynthia J;
    • Siguero, Juan Pedro López
    Publication type:
    Correction Notice
    38

    Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 75, doi. 10.1038/ng1939
    By:
    • Tartaglia, Marco;
    • Pennacchio, Len A.;
    • Zhao, Chen;
    • Yadav, Kamlesh K.;
    • Fodale, Valentina;
    • Sarkozy, Anna;
    • Pandit, Bhaswati;
    • Oishi, Kimihiko;
    • Martinelli, Simone;
    • Schackwitz, Wendy;
    • Ustaszewska, Anna;
    • Martin, Joel;
    • Bristow, James;
    • Carta, Claudio;
    • Lepri, Francesca;
    • Neri, Cinzia;
    • Vasta, Isabella;
    • Gibson, Kate;
    • Curry, Cynthia J.;
    • Siguero, Juan Pedro López
    Publication type:
    Article
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    Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation.

    Published in:
    Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1231434
    By:
    • Zuntini, Roberta;
    • Cattani, Chiara;
    • Pedace, Lucia;
    • Miele, Evelina;
    • Caraffi, Stefano Giuseppe;
    • Gardini, Stefano;
    • Ficarelli, Elena;
    • Pizzi, Simone;
    • Radio, Francesca Clementina;
    • Barone, Angelica;
    • Piana, Simonetta;
    • Bertolini, Patrizia;
    • Corradi, Domenico;
    • Marinelli, Maria;
    • Longo, Caterina;
    • Motolese, Alberico;
    • Zuffardi, Orsetta;
    • Tartaglia, Marco;
    • Garavelli, Livia
    Publication type:
    Article
    42

    Reversing vemurafenib‐resistance in primary melanoma cells by combined romidepsin and type I IFN treatment through blocking of tumorigenic signals and induction of immunogenic effects.

    Published in:
    International Journal of Cancer, 2023, v. 153, n. 5, p. 1080, doi. 10.1002/ijc.34602
    By:
    • Fragale, Alessandra;
    • Stellacci, Emilia;
    • Romagnoli, Giulia;
    • Licursi, Valerio;
    • Parlato, Stefania;
    • Canini, Irene;
    • Remedi, Giacomo;
    • Buoncervello, Maria;
    • Matarrese, Paola;
    • Pedace, Lucia;
    • Ascione, Barbara;
    • Pizzi, Simone;
    • Tartaglia, Marco;
    • D'Atri, Stefania;
    • Presutti, Carlo;
    • Capone, Imerio;
    • Gabriele, Lucia
    Publication type:
    Article
    43

    Upfront treatment with mTOR inhibitor everolimus in pediatric low-grade gliomas: A single-center experience.

    Published in:
    International Journal of Cancer, 2021, v. 148, n. 10, p. 2522, doi. 10.1002/ijc.33438
    By:
    • Cacchione, Antonella;
    • Lodi, Mariachiara;
    • Carai, Andrea;
    • Miele, Evelina;
    • Tartaglia, Marco;
    • Megaro, Giacomina;
    • Baldo, Giada Del;
    • Alessi, Iside;
    • Colafati, Giovanna Stefania;
    • Carboni, Alessia;
    • Boccuto, Luigi;
    • Camassei, Francesca Diomedi;
    • Catanzaro, Giuseppina;
    • Po, Agnese;
    • Ferretti, Elisabetta;
    • Pedace, Lucia;
    • Pizzi, Simone;
    • Folgiero, Valentina;
    • Pezzullo, Marco;
    • Corsetti, Tiziana
    Publication type:
    Article
    44

    Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures.

    Published in:
    Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1207176
    By:
    • Cesaroni, Carlo Alberto;
    • Pollazzon, Marzia;
    • Mancini, Cecilia;
    • Rizzi, Susanna;
    • Cappelletti, Camilla;
    • Pizzi, Simone;
    • Frattini, Daniele;
    • Spagnoli, Carlotta;
    • Caraffi, Stefano Giuseppe;
    • Zuntini, Roberta;
    • Trimarchi, Gabriele;
    • Niceta, Marcello;
    • Radio, Francesca Clementina;
    • Tartaglia, Marco;
    • Garavelli, Livia;
    • Fusco, Carlo
    Publication type:
    Article
    45

    Nerve enlargement in patients with Noonan syndrome: A retrospective cohort study.

    Published in:
    American Journal of Medical Genetics. Part A, 2024, v. 194, n. 11, p. 1, doi. 10.1002/ajmg.a.63810
    By:
    • Draaisma, Fieke;
    • Leenders, Erika K. S. M.;
    • Erasmus, Corrie E.;
    • Braakman, Hilde M. H.;
    • Burgers, Melanie C. J.;
    • Coppens, Catelijne H.;
    • Rinne, Tuula;
    • Zenker, Martin;
    • Tartaglia, Marco;
    • Reintjes, Wesley;
    • Voermans, Nicol C.;
    • van Engelen, Baziel G. M.;
    • van Alfen, Nens;
    • Draaisma, Jos M. T.
    Publication type:
    Article
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    Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic POLR2A variant.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 9, p. 2796, doi. 10.1002/ajmg.a.62869
    By:
    • Paparella, Roberto;
    • Caroleo, Anna Maria;
    • Agolini, Emanuele;
    • Chillemi, Giovanni;
    • Miele, Evelina;
    • Pedace, Lucia;
    • Rinelli, Martina;
    • Pizzi, Simone;
    • Boccuto, Luigi;
    • Colafati, Giovanna Stefania;
    • Lodi, Mariachiara;
    • Cacchione, Antonella;
    • Carai, Andrea;
    • Digilio, Maria Cristina;
    • Tomà, Paolo;
    • Tartaglia, Marco;
    • Mastronuzzi, Angela
    Publication type:
    Article
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