The Corrosion Behaviour of Additively Manufactured AlSi10Mg Parts Compared to Traditional Al Alloys
Gatto, Andrea, Cappelletti, Camilla, Defanti, Silvio, Fabbri, Fabrizio
Published in Metals (Basel ) (01.05.2023)
Published in Metals (Basel ) (01.05.2023)
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Journal Article
Venom immunotherapy: safety and tolerability of the build‐up phase with depot versus aqueous preparations
Valerio, Pravettoni, Marina, Mauro, Federica, Rivolta, Dario, Consonni, Camilla, Cappelletti, Alessandra, Chiei Gallo, Andrea, Sangalli, Maria, Bilò Beatrice
Published in Clinical and experimental allergy (01.10.2022)
Published in Clinical and experimental allergy (01.10.2022)
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Journal Article
Boosting Productivity of Laser Powder Bed Fusion for AlSi10Mg
Defanti, Silvio, Cappelletti, Camilla, Gatto, Andrea, Tognoli, Emanuele, Fabbri, Fabrizio
Published in Journal of Manufacturing and Materials Processing (01.10.2022)
Published in Journal of Manufacturing and Materials Processing (01.10.2022)
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Journal Article
Case report: Expanding the phenotype of FOXP1 -related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures
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
Published in Frontiers in neurology (14.07.2023)
Published in Frontiers in neurology (14.07.2023)
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Journal Article
Successful fractionated undiluted doses of COVID‐19 vaccine in five cases of suspected allergic reactions to the first dose
Rivolta, Federica, Camilla, Cappelletti, Sangalli, Andrea, Chiei Gallo, Alessandra, Pravettoni, Valerio
Published in Clinical case reports (01.10.2022)
Published in Clinical case reports (01.10.2022)
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Journal Article
Successful adalimumab graded challenge after allergic delayed reaction to golimumab in a woman with rheumatoid arthritis
Rivolta, Federica, Sangalli, Andrea, Cappelletti, Camilla, Chiei Gallo, Alessandra, Dubini, Marco, Pravettoni, Valerio
Published in Clinical case reports (01.03.2023)
Published in Clinical case reports (01.03.2023)
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Journal Article
A comprehensive molecular approach in fish allergy: Usefulness in daily clinical practice
Villalta, Danilo, Scala, Enrico, Deleonardi, Gaia, Busa, Moira, Rivolta, Federica, Boni, Elisa, Gabrielli, Giulia, Farioli, Laura, Cappelletti, Camilla, Buzzulini, Francesca, Conte, Mariaelisabetta, Pravettoni, Valerio, Asero, Riccardo
Published in Clinica chimica acta (01.08.2022)
Published in Clinica chimica acta (01.08.2022)
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Journal Article
Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features
Priolo, Manuela, Mancini, Cecilia, Radio, Francesca Clementina, Chiriatti, Luigi, Ciolfi, Andrea, Cappelletti, Camilla, Cordeddu, Viviana, Pintomalli, Letizia, Brusco, Alfredo, Mammi, Corrado, Tartaglia, Marco
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2023)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2023)
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Journal Article
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism
Niceta, Marcello, Ciolfi, Andrea, Ferilli, Marco, Pedace, Lucia, Cappelletti, Camilla, Nardini, Claudia, Hildonen, Mathis, Chiriatti, Luigi, Miele, Evelina, Dentici, Maria Lisa, Gnazzo, Maria, Cesario, Claudia, Pisaneschi, Elisa, Baban, Anwar, Novelli, Antonio, Maitz, Silvia, Selicorni, Angelo, Squeo, Gabriella Maria, Merla, Giuseppe, Dallapiccola, Bruno, Tumer, Zeynep, Digilio, Maria Cristina, Priolo, Manuela, Tartaglia, Marco
Published in European journal of human genetics : EJHG (01.07.2024)
Published in European journal of human genetics : EJHG (01.07.2024)
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Journal Article
Identification of a robust DNA methylation signature for Fanconi anemia
Pagliara, Daria, Ciolfi, Andrea, Pedace, Lucia, Haghshenas, Sadegheh, Ferilli, Marco, Levy, Michael A., Miele, Evelina, Nardini, Claudia, Cappelletti, Camilla, Relator, Raissa, Pitisci, Angela, De Vito, Rita, Pizzi, Simone, Kerkhof, Jennifer, McConkey, Haley, Nazio, Francesca, Kant, Sarina G., Di Donato, Maddalena, Agolini, Emanuele, Matraxia, Marta, Pasini, Barbara, Pelle, Alessandra, Galluccio, Tiziana, Novelli, Antonio, Barakat, Tahsin Stefan, Andreani, Marco, Rossi, Francesca, Mecucci, Cristina, Savoia, Anna, Sadikovic, Bekim, Locatelli, Franco, Tartaglia, Marco
Published in American journal of human genetics (02.11.2023)
Published in American journal of human genetics (02.11.2023)
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Journal Article
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis
Dentici, Maria Lisa, Niceta, Marcello, Lepri, Francesca Romana, Mancini, Cecilia, Priolo, Manuela, Bonnard, Adeline Alice, Cappelletti, Camilla, Leoni, Chiara, Ciolfi, Andrea, Pizzi, Simone, Cordeddu, Viviana, Rossi, Cesare, Ferilli, Marco, Mucciolo, Mafalda, Colona, Vito Luigi, Fauth, Christine, Bellini, Melissa, Biasucci, Giacomo, Sinibaldi, Lorenzo, Briuglia, Silvana, Gazzin, Andrea, Carli, Diana, Memo, Luigi, Trevisson, Eva, Schiavariello, Concetta, Luca, Maria, Novelli, Antonio, Michot, Caroline, Sweertvaegher, Anne, Germanaud, David, Scarano, Emanuela, De Luca, Alessandro, Zampino, Giuseppe, Zenker, Martin, Mussa, Alessandro, Dallapiccola, Bruno, Cavé, Helene, Digilio, Maria Cristina, Tartaglia, Marco
Published in European journal of human genetics : EJHG (01.08.2024)
Published in European journal of human genetics : EJHG (01.08.2024)
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Journal Article
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants
Ferilli, Marco, Ciolfi, Andrea, Pedace, Lucia, Niceta, Marcello, Radio, Francesca Clementina, Pizzi, Simone, Miele, Evelina, Cappelletti, Camilla, Mancini, Cecilia, Galluccio, Tiziana, Andreani, Marco, Iascone, Maria, Chiriatti, Luigi, Novelli, Antonio, Micalizzi, Alessia, Matraxia, Marta, Menale, Lucia, Faletra, Flavio, Prontera, Paolo, Pilotta, Alba, Bedeschi, Maria Francesca, Capolino, Rossella, Baban, Anwar, Seri, Marco, Mammì, Corrado, Zampino, Giuseppe, Digilio, Maria Cristina, Dallapiccola, Bruno, Priolo, Manuela, Tartaglia, Marco
Published in Genes (19.11.2022)
Published in Genes (19.11.2022)
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Journal Article
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying INSD1/I Variants
Ferilli, Marco, Ciolfi, Andrea, Pedace, Lucia, Niceta, Marcello, Radio, Francesca Clementina, Pizzi, Simone, Miele, Evelina, Cappelletti, Camilla, Mancini, Cecilia, Galluccio, Tiziana, Andreani, Marco, Iascone, Maria, Chiriatti, Luigi, Novelli, Antonio, Micalizzi, Alessia, Matraxia, Marta, Menale, Lucia, Faletra, Flavio, Prontera, Paolo, Pilotta, Alba, Bedeschi, Maria Francesca, Capolino, Rossella, Baban, Anwar, Seri, Marco, Mammì, Corrado, Zampino, Giuseppe, Digilio, Maria Cristina, Dallapiccola, Bruno, Priolo, Manuela, Tartaglia, Marco
Published in Genes (01.11.2022)
Published in Genes (01.11.2022)
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Journal Article
Successful adalimumab graded challenge after allergic delayed reaction to golimumab in a woman with rheumatoid arthritis
Rivolta, Federica, Sangalli, Andrea, Cappelletti, Camilla, Chiei Gallo, Alessandra, Dubini, Marco, Pravettoni, Valerio
Published in Clinical case reports (01.03.2023)
Published in Clinical case reports (01.03.2023)
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Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures
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
Published in Frontiers in neurology (01.01.2023)
Published in Frontiers in neurology (01.01.2023)
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