Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sara Naldini"'
Autor:
Giulia Trippella, Paolo Lionetti, Sara Naldini, Francesca Peluso, Matteo Della Monica, Stefano Stagi
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-7 (2018)
Abstract Background Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant disorder caused by defects involving the TRPS1 gene. It exhibits distinctive craniofacial, ectodermal and skeletal abnormalities, such as sparse hair, bulbous nasa
Externí odkaz:
https://doaj.org/article/8828fe3836ef4d7ea279a9acbd9be95d
Autor:
Riccardo Morganti, Ivano Biviano, Siro Bagnoli, Francesca Calella, Sara Naldini, E.N. Lynch, Lorenzo Bertani, Linda Ceccarelli, Paolo Lionetti, Simona Maltinti, Alberto Pieraccini, G. Tapete, Moira Minciotti, Francesca De Nigris, Martina Giannotta, Francesco Costa, Maria Gloria Mumolo, Monica Milla, Silvia Rentini
Publikováno v:
Inflammatory Bowel Diseases. 28:62-69
Background Few data are currently available about SB5 in inflammatory bowel diseases (IBD). The aim of this study was to assess the effectiveness and safety of SB5 in a cohort of patients with IBD in stable remission switched from the adalimumab (ADA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b74f862fee62621fb769e9647058a99
https://doi.org/10.1093/ibd/izab027
https://doi.org/10.1093/ibd/izab027
Autor:
Jacopo Barp, Sara Naldini, Giulia Bolasco, Salvatore De Masi, Sara Renzo, P. Alvisi, Paolo Lionetti, Luca Scarallo, Marcello Lanari, Monica Paci, Alice Cangiari, Michele Di Toma
OBJECTIVES Mucosal healing (MH) and histological healing (HH) have been recently proposed as a novel treatment target for inflammatory bowel disease (IBD). The aim of the present study was to evaluate real-life achievement of such outcomes in a cohor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::833717225177debd97b41d5e8270f605
http://hdl.handle.net/11585/809830
http://hdl.handle.net/11585/809830
Autor:
Luca Scarallo, Monica Di Paola, Sara Naldini, Martina Bianconi, Sara Renzo, Patrizia Alvisi, Michele Di Toma, Monica Paci, Giulia Bolasco, Flavio Labriola, Paolo Lionetti, Jacopo Barp, Salvatore De Masi
Publikováno v:
Inflammatory bowel diseases. 28(2)
Background The aim of the present study was to investigate outcomes of anti-TNF-alpha (ATA) withdrawal in selected pediatric patients with inflammatory bowel disease who achieved clinical remission and mucosal and histological healing (MH and HH). Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867bf7f3bd492b3daf094791a1f1abc2
https://pubmed.ncbi.nlm.nih.gov/33835170
https://pubmed.ncbi.nlm.nih.gov/33835170
Autor:
Luca Scarallo, Monica Paci, Valerio Maniscalco, Sara Renzo, Laura Tasciotti, Paolo Lionetti, Jacopo Barp, Sara Naldini
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 71(1)
Acute severe colitis (ASC) is a potentially life-threatening event. Optimal timing for second-line treatment in children is mainly based on the clinical score Pediatric Ulcerative Colitis Activity Index. The aim of our study was to evaluate the poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::674679bf8461c67da2fc7a808faf00de
https://pubmed.ncbi.nlm.nih.gov/32102087
https://pubmed.ncbi.nlm.nih.gov/32102087
Autor:
Sara Naldini, Matteo Della Monica, Francesca Peluso, Giulia Trippella, Paolo Lionetti, Stefano Stagi
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-7 (2018)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
Background Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant disorder caused by defects involving the TRPS1 gene. It exhibits distinctive craniofacial, ectodermal and skeletal abnormalities, such as sparse hair, bulbous nasal tip and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c247ec86f93400992e71572c329da8d
http://link.springer.com/article/10.1186/s13052-018-0580-z
http://link.springer.com/article/10.1186/s13052-018-0580-z