Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Di Candia, Stefania"'
Autor:
Mussa, Alessandro, Di Candia, Stefania, Russo, Silvia, Catania, Serena, De Pellegrin, Maurizio, Di Luzio, Luisa, Ferrari, Mario, Tortora, Chiara, Meazzini, Maria Costanza, Brusati, Roberto, Milani, Donatella, Zampino, Giuseppe, Montirosso, Rosario, Riccio, Andrea, Selicorni, Angelo, Cocchi, Guido, Ferrero, Giovanni Battista
Publikováno v:
In European Journal of Medical Genetics January 2016 59(1):52-64
Publikováno v:
Journal of Obesity, Vol 2012 (2012)
Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient’s life. The syndrome is due to the loss of expression of several genes encoded on the proximal long
Externí odkaz:
https://doaj.org/article/2bb4dc9ad2dc462a84b89f2d187c73b6
Autor:
Grugni, Graziano, Licenziati, Maria Rosaria, Valerio, Giuliana, Crinò, Antonino, Maffeis, Claudio, Tanas, Rita, Morino, Giuseppe Stefano, Ambruzzi, Amalia, Balsamo, Antonio, Bellone, Simonetta, Bernasconi, Sergio, Bianchi, Vanessa, Bobbio, Adriana, Bruzzi, Patrizia, Buongiovanni, Carmen, Calcagno, Annalisa, Calcaterra, Valeria, Canali, Teresa, Cerutti, Franco, Corciulo, Nicola, Cotugno, Fortunato, Cuccarolo, Giuliano, D’Amico, Osvaldo, Di Bonito, Procolo, Di Candia, Stefania, Di Pietrantonio, Violetta, Di Pietro, Mario, Filannino, Grazia, Fintini, Danilo, Forziato, Claudia, Franceschi, Roberto, Franzese, Adriana, Galeazzi, Daniela, Gargantini, Luigi, Franca Giusti, Lia, Gualtieri, Antonella, Laura Iezzi, Maria, Iughetti, Lorenzo, Lera, Riccardo, Limauro, Raffaele, Lombardi, Francesca, Lucchesi, Sonia, Macchiaroli, Annamaria, Maltoni, Giulio, Manco, Melania, MIRAGLIA DEL GIUDICE, Emanuele, Modestini, Elisabetta, Morandi, Anita, Mozzillo, Enza, Nanni, Laura, Nicolosi, Alessandra, Pellegrin, Maria Chiara, Peruzzi, Sonia, Peverelli, Paola, Purromuto, Salvatore, Ragusa, Letizia, Rosato, Teresa, Salvo, Caterina, Sartori, Chiara, Sticco, Maura, Elisabeth Street, Maria, Trifirò, Giuliana, Vianelli, Patrizia, Yiannakou, Pietro, IAFUSCO, Dario
Severe/medically complicated obesity in childhood, and particularly in adolescence, is a real disability that requires an intensive and continuous approach which should follow the procedures and schedule of rehabilitation medicine. Given the lack of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aac48c5697068b2b25cc06fc92b314b
http://hdl.handle.net/11591/371193
http://hdl.handle.net/11591/371193
Autor:
Russo, Silvia, Calzari, Luciano, Mussa, Alessandro, Mainini, Ester, Cassina, Matteo, Di Candia, Stefania, Clementi, Maurizio, Guzzetti, Sara, Tabano, Silvia, Miozzo, Monica, Sirchia, Silvia, Finelli, Palma, Prontera, Paolo, Maitz, Silvia, Sorge, Giovanni, Calcagno, Annalisa, Maghnie, Mohamad, Divizia, Maria Teresa, Melis, Daniela, Manfredini, Emanuela, Ferrero, Giovanni Battista, Pecile, Vanna, Larizza, Lidia
Publikováno v:
Clinical Epigenetics
Background Multiple (epi)genetic defects affecting the expression of the imprinted genes within the 11p15.5 chromosomal region underlie Silver–Russell (SRS) and Beckwith–Wiedemann (BWS) syndromes. The molecular diagnosis of these opposite growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e2a725bebca7a5951eaccd2a30c36f6c
http://hdl.handle.net/11386/4760493
http://hdl.handle.net/11386/4760493
Autor:
Salvatoni, Alessandro, Bocchini, Sarah, Crinò, Antonino, Di Candia, Stefania, Grugni, Graziano, Iughetti, Lorenzo, Nespoli, Luigi, Nosetti, Luana, Padoan, Giovanni, Pilotta, Alba, Piran, Marzia, Spica Russotto, Valeria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3660::29ec40d95a8a82b9c2a0fb5bcaeeaa73
http://hdl.handle.net/11383/2026937
http://hdl.handle.net/11383/2026937
Autor:
Grugni, Graziano, Corrias, Andrea, Di Candia, Stefania, Fintini, Danilo, Gargantini, Luigi, Iughetti, Lorenzo, Ragusa, Letizia, Salvatoni, Alessandro, Sartorio, Alessandro, Bocchini, Sarah, Delvecchio, Maurizio, Chiumello, Giuseppe, Crinò, Antonino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3660::551b63aec2820be9e5b28dd8558f3853
http://hdl.handle.net/11383/2026934
http://hdl.handle.net/11383/2026934
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Obesity
Journal of Obesity, Vol 2012 (2012)
Journal of Obesity, Vol 2012 (2012)
Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient’s life. The syndrome is due to the loss of expression of several genes encoded on the proximal long
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc908c13ea01701cdca2cf95aa598aab
https://pubmed.ncbi.nlm.nih.gov/23133744
https://pubmed.ncbi.nlm.nih.gov/23133744
Autor:
Grugni, Graziano, Crino, Antonino, Bedogni, Giorgio, Bosio, Laura, Cappa, Marco, Corrias, Andrea, Delvecchio, Maurizio, Di Candia, Stefania, Gargantini, Luigi, Iughetti, Lorenzo, Letizia Ragusa, Sacco, Michele, Salvatoni, Alessandro, Sartorio, Alessandro, Chiumello, Giuseppe, Brambilla, Paolo
Publikováno v:
Web of Science
Publons
ResearcherID
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Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2dac3f1e1d47c09d7aa76c3261de7c40
http://hdl.handle.net/11383/1714654
http://hdl.handle.net/11383/1714654