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Published in Angewandte Chemie International Edition (18.11.2019)
Published in Angewandte Chemie International Edition (18.11.2019)
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Schiaffino, Simone, Calabrese, Massimo, Melani, Enrico Francesco, Trimboli, Rubina Manuela, Cozzi, Andrea, Carbonaro, Luca Alessandro, Di Leo, Giovanni, Sardanelli, Francesco
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Published in Radiology (01.01.2020)
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Unbalanced, cracked, and misaligned rotating machines: a comparison between classification procedures throughout the steady-state operation
Rezazadeh, Nima, De Luca, Alessandro, Perfetto, Donato
Published in Journal of the Brazilian Society of Mechanical Sciences and Engineering (01.10.2022)
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Haddadin, Sami, De Luca, Alessandro, Albu-Schaffer, Alin
Published in IEEE transactions on robotics (01.12.2017)
Published in IEEE transactions on robotics (01.12.2017)
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Published in Insights into imaging (02.08.2019)
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Regioselective functionalization of aryl azoles as powerful tool for the synthesis of pharmaceutically relevant targets
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Published in Nature communications (07.09.2020)
Published in Nature communications (07.09.2020)
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Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome
Cordeddu, Viviana, Yin, Jiani C., Gunnarsson, Cecilia, Virtanen, Carl, Drunat, Séverine, Lepri, Francesca, De Luca, Alessandro, Rossi, Cesare, Ciolfi, Andrea, Pugh, Trevor J., Bruselles, Alessandro, Priest, James R., Pennacchio, Len A., Lu, Zhibin, Danesh, Arnavaz, Quevedo, Rene, Hamid, Alaa, Martinelli, Simone, Pantaleoni, Francesca, Gnazzo, Maria, Daniele, Paola, Lissewski, Christina, Bocchinfuso, Gianfranco, Stella, Lorenzo, Odent, Sylvie, Philip, Nicole, Faivre, Laurence, Vlckova, Marketa, Seemanova, Eva, Digilio, Cristina, Zenker, Martin, Zampino, Giuseppe, Verloes, Alain, Dallapiccola, Bruno, Roberts, Amy E., Cavé, Hélène, Gelb, Bruce D., Neel, Benjamin G., Tartaglia, Marco
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Published in Human mutation (01.11.2015)
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Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS)
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Published in International journal of molecular sciences (26.01.2021)
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CD73 expression and pathologic response to neoadjuvant chemotherapy in triple negative breast cancer
Cerbelli, Bruna, Botticelli, Andrea, Pisano, Annalinda, Pernazza, Angelina, Campagna, Domenico, De Luca, Alessandro, Ascierto, Paolo Antonio, Pignataro, Maria Gemma, Pelullo, Maria, Rocca, Carlo Della, Marchetti, Paolo, Fortunato, Lucio, Costarelli, Leopoldo, d’Amati, Giulia
Published in Virchows Archiv : an international journal of pathology (01.04.2020)
Published in Virchows Archiv : an international journal of pathology (01.04.2020)
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METhodological RadiomICs Score (METRICS): a quality scoring tool for radiomics research endorsed by EuSoMII
Kocak, Burak, Akinci D’Antonoli, Tugba, Mercaldo, Nathaniel, Alberich-Bayarri, Angel, Baessler, Bettina, Ambrosini, Ilaria, Andreychenko, Anna E., Bakas, Spyridon, Beets-Tan, Regina G. H., Bressem, Keno, Buvat, Irene, Cannella, Roberto, Cappellini, Luca Alessandro, Cavallo, Armando Ugo, Chepelev, Leonid L., Chu, Linda Chi Hang, Demircioglu, Aydin, deSouza, Nandita M., Dietzel, Matthias, Fanni, Salvatore Claudio, Fedorov, Andrey, Fournier, Laure S., Giannini, Valentina, Girometti, Rossano, Groot Lipman, Kevin B. W., Kalarakis, Georgios, Kelly, Brendan S., Klontzas, Michail E., Koh, Dow-Mu, Kotter, Elmar, Lee, Ho Yun, Maas, Mario, Marti-Bonmati, Luis, Müller, Henning, Obuchowski, Nancy, Orlhac, Fanny, Papanikolaou, Nikolaos, Petrash, Ekaterina, Pfaehler, Elisabeth, Pinto dos Santos, Daniel, Ponsiglione, Andrea, Sabater, Sebastià, Sardanelli, Francesco, Seeböck, Philipp, Sijtsema, Nanna M., Stanzione, Arnaldo, Traverso, Alberto, Ugga, Lorenzo, Vallières, Martin, van Dijk, Lisanne V., van Griethuysen, Joost J. M., van Hamersvelt, Robbert W., van Ooijen, Peter, Vernuccio, Federica, Wang, Alan, Williams, Stuart, Witowski, Jan, Zhang, Zhongyi, Zwanenburg, Alex, Cuocolo, Renato
Published in Insights into imaging (17.01.2024)
Published in Insights into imaging (17.01.2024)
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Clinical and functional characterization of a novel RASopathy‐causing SHOC2 mutation associated with prenatal‐onset hypertrophic cardiomyopathy
Motta, Marialetizia, Giancotti, Antonella, Mastromoro, Gioia, Chandramouli, Balasubramanian, Pinna, Valentina, Pantaleoni, Francesca, Di Giosaffatte, Niccolò, Petrini, Stefania, Mazza, Tommaso, D’Ambrosio, Valentina, Versacci, Paolo, Ventriglia, Flavia, Chillemi, Giovanni, Pizzuti, Antonio, Tartaglia, Marco, Luca, Alessandro
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Published in Human mutation (01.08.2019)
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P2RY1/ALK3-Expressing Cells within the Adult Human Exocrine Pancreas Are BMP-7 Expandable and Exhibit Progenitor-like Characteristics
Qadir, Mirza Muhammad Fahd, Álvarez-Cubela, Silvia, Klein, Dagmar, Lanzoni, Giacomo, García-Santana, Carlos, Montalvo, Abelardo, Pláceres-Uray, Fabiola, Mazza, Emilia Maria Cristina, Ricordi, Camillo, Inverardi, Luca Alessandro, Pastori, Ricardo Luis, Domínguez-Bendala, Juan
Published in Cell reports (Cambridge) (27.02.2018)
Published in Cell reports (Cambridge) (27.02.2018)
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Coincidental or Causal? Concurrence of Colorectal Carcinoma with Primary Breast Cancer
Tripodi, Domenico, Cannistra’, Claudio, Gagliardi, Federica, Casella, Giovanni, Lauro, Augusto, De Luca, Alessandro, Amabile, Maria Ida, Palumbo, Piergaspare, Pironi, Daniele, Mascagni, Domenico, D’Andrea, Vito, Vergine, Massimo, Sorrenti, Salvatore
Published in Digestive diseases and sciences (01.02.2022)
Published in Digestive diseases and sciences (01.02.2022)
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Focal Liver Lesions in Budd-Chiari Syndrome: Spectrum of Imaging Findings
Rizzetto, Francesco, Rutanni, Davide, Carbonaro, Luca Alessandro, Vanzulli, Angelo
Published in Diagnostics (Basel) (01.07.2023)
Published in Diagnostics (Basel) (01.07.2023)
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Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome
Pannone, Luca, Bocchinfuso, Gianfranco, Flex, Elisabetta, Rossi, Cesare, Baldassarre, Giuseppina, Lissewski, Christina, Pantaleoni, Francesca, Consoli, Federica, Lepri, Francesca, Magliozzi, Monia, Anselmi, Massimiliano, Delle Vigne, Silvia, Sorge, Giovanni, Karaer, Kadri, Cuturilo, Goran, Sartorio, Alessandro, Tinschert, Sigrid, Accadia, Maria, Digilio, Maria C., Zampino, Giuseppe, Luca, Alessandro, Cavé, Hélène, Zenker, Martin, Gelb, Bruce D., Dallapiccola, Bruno, Stella, Lorenzo, Ferrero, Giovanni B., Martinelli, Simone, Tartaglia, Marco
Published in Human mutation (01.04.2017)
Published in Human mutation (01.04.2017)
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Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications
Lissewski, Christina, Chune, Valérie, Pantaleoni, Francesca, De Luca, Alessandro, Capri, Yline, Brinkmann, Julia, Lepri, Francesca, Daniele, Paola, Leenders, Erika, Mazzanti, Laura, Scarano, Emanuela, Radio, Francesca Clementina, Kutsche, Kerstin, Kuechler, Alma, Gérard, Marion, Ranguin, Kara, Legendre, Marine, Vial, Yoann, van der Burgt, Ineke, Rinne, Tuula, Andreucci, Elena, Mastromoro, Gioia, Digilio, Maria Cristina, Cave, Hélène, Tartaglia, Marco, Zenker, Martin
Published in European journal of human genetics : EJHG (01.01.2021)
Published in European journal of human genetics : EJHG (01.01.2021)
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Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect
Ferese, Rosangela, Bonetti, Monica, Consoli, Federica, Guida, Valentina, Sarkozy, Anna, Lepri, Francesca Romana, Versacci, Paolo, Gambardella, Stefano, Calcagni, Giulio, Margiotti, Katia, Piceci Sparascio, Francesca, Hozhabri, Hossein, Mazza, Tommaso, Digilio, Maria Cristina, Dallapiccola, Bruno, Tartaglia, Marco, Marino, Bruno, Hertog, Jeroen den, Luca, Alessandro
Published in Human mutation (01.10.2018)
Published in Human mutation (01.10.2018)
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