Bibliotecas PUC-SP - Busca Integrada

A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

od Alessia Aureli, Sarah Bocchini, Michela Mariani, Antonino Crinò, Marco Cappa, Danilo Fintini
izdano v Frontiers in Endocrinology (2023-04-01)

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report

od Sarah Bocchini, Danilo Fintini, Graziano Grugni, Arianna Boiani, Alessio Convertino, Antonino Crinò
izdano v Italian Journal of Pediatrics (2017-09-01)

The impact of IGF-I, puberty and obesity on early retinopathy in children: a cross-sectional study

od Carla Bizzarri, Stefania Pedicelli, Antonino Romanzo, Sarah Bocchini, Giorgia Bottaro, Stefano Cianfarani, Marco Cappa
izdano v Italian Journal of Pediatrics (2019-04-01)

High Prevalence of Scoliosis in a Large Cohort of Patients with Prader-Willi Syndrome

od Antonino Crinò, Michela Armando, Marco Crostelli, Osvaldo Mazza, Dario Bruzzese, Alessio Convertino, Danilo Fintini, Sarah Bocchini, Sara Ciccone, Alessandro Sartorio, Graziano Grugni
izdano v Journal of Clinical Medicine (2022-03-01)

Circulating Irisin in Children and Adolescents With Prader-Willi Syndrome: Relation With Glucose Metabolism

od Stefania Mai, Danilo Fintini, Chiara Mele, Alessio Convertino, Sarah Bocchini, Graziano Grugni, Gianluca Aimaretti, Roberta Vietti, Massimo Scacchi, Massimo Scacchi, Antonino Crinò, Paolo Marzullo, Paolo Marzullo
izdano v Frontiers in Endocrinology (2022-06-01)

AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial.

od Soraya Allas, Assumpta Caixàs, Christine Poitou, Muriel Coupaye, Denise Thuilleaux, Françoise Lorenzini, Gwenaëlle Diene, Antonino Crinò, Frédéric Illouz, Graziano Grugni, Diane Potvin, Sarah Bocchini, Thomas Delale, Thierry Abribat, Maithé Tauber
izdano v PLoS ONE (2018-01-01)

The Italian registry for patients with Prader–Willi syndrome

od Marco Salvatore, Paola Torreri, Graziano Grugni, Adele Rocchetti, Mohamad Maghnie, Giuseppa Patti, Antonino Crinò, Maurizio Elia, Donatella Greco, Corrado Romano, Adriana Franzese, Enza Mozzillo, Annamaria Colao, Gabriella Pugliese, Uberto Pagotto, Valentina Lo Preiato, Emanuela Scarano, Concetta Schiavariello, Gianluca Tornese, Danilo Fintini, Sarah Bocchini, Sara Osimani, Luisa De Sanctis, Michele Sacco, Irene Rutigliano, Maurizio Delvecchio, Maria Felicia Faienza, Malgorzata Wasniewska, Domenico Corica, Stefano Stagi, Laura Guazzarotti, Pietro Maffei, Francesca Dassie, Domenica Taruscio
izdano v Orphanet Journal of Rare Diseases (2023-02-01)

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation

od Simona F. Madeo, Luca Zagaroli, Sara Vandelli, Valeria Calcaterra, Valeria Calcaterra, Antonino Crinò, Luisa De Sanctis, Maria Felicia Faienza, Danilo Fintini, Laura Guazzarotti, Maria Rosaria Licenziati, Enza Mozzillo, Roberta Pajno, Emanuela Scarano, Maria E. Street, Maria E. Street, Malgorzata Wasniewska, Malgorzata Wasniewska, Sarah Bocchini, Carmen Bucolo, Raffaele Buganza, Mariangela Chiarito, Domenico Corica, Domenico Corica, Francesca Di Candia, Roberta Francavilla, Nadia Fratangeli, Nicola Improda, Letteria A. Morabito, Chiara Mozzato, Virginia Rossi, Concetta Schiavariello, Giovanni Farello, Lorenzo Iughetti, Vincenzo Salpietro, Alessandro Salvatoni, Mara Giordano, Mara Giordano, Graziano Grugni, Maurizio Delvecchio
izdano v Frontiers in Endocrinology (2024-04-01)