Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sara Azzolini"'
Autor:
Mariacarolina Salerno, Giuseppa Patti, Mohamad Maghnie, Sara Azzolini, Silvia Longhi, Alessandra di Lascio, Gianni Russo, Corrado Betterle, Giusy Ferro, Carla Bizzarri, Marco Cappa, Giorgio Radetti, Marianna Rita Stancampiano, Mariella Valenzise, Donatella Capalbo, Cristina Moracas, Antonio Balsamo, Nella Augusta Greggio, Malgorzata Wasniewska, Federico Baronio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 106:762-773
Context Primary adrenal insufficiency (PAI) is a rare and potentially life-threatening condition that is poorly characterized in children. Objective To describe causes, presentation, auxological outcome, frequency of adrenal crisis and mortality of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27b859b910ae8749c045fea7c3e7dbc0
https://doi.org/10.1210/clinem/dgaa881
https://doi.org/10.1210/clinem/dgaa881
Autor:
Luana Nosetti, Sara Azzolini, Simona Filomena Madeo, Valentina Bonaita, S. Ferraris, Paola Cianci, Alessandro Salvatoni, Silvia Salvatore, Irene Rutigliano, Antonino Crinò, Graziano Grugni, G. Trifirò, Maurizio Delvecchio, Michele Sacco, Roberta Pajno, Lorenzo Iughetti, Alex Moretti, Nella Augusta Greggio, Domenico Corica, Malgorzata Wasniewska, Maria Rosaria Licenziati, Emanuela Scarano, Massimo Agosti
This is a retrospective multicenter nationwide Italian study collecting neonatal anthropometric data of Caucasian subjects with Prader–Willi syndrome (PWS) born from 1988 to 2018. The aim of the study is to provide percentile charts for weight and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3934661885522c9b1a6cbc0bb4227ef8
http://hdl.handle.net/11570/3143013
http://hdl.handle.net/11570/3143013
Autor:
Renzo Manara, Margherita Nosadini, Aglaia Vignoli, Davide Brotto, Maria Federica Pelizza, Cecilia Parazzini, Paola Canevini, Francesca Labriola, Sara Azzolini, Samuela Bugin, Irene Toldo, Angela Peron, Giorgio Iaconetta, Alessandra Murgia, Stefano Sartori
Publikováno v:
Neuroradiology. 60(8)
Despite complex olfactory bulb embryogenesis, its development abnormalities in tuberous sclerosis complex (TSC) have been poorly investigated. Brain MRIs of 110 TSC patients (mean age 11.5 years; age range 0.5–38 years; 52 female; 26 TSC1, 68 TSC2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bedaa0c4bd627348b4703a2462882dd7
https://pubmed.ncbi.nlm.nih.gov/29909560
https://pubmed.ncbi.nlm.nih.gov/29909560
Autor:
Francesco Fallo, Roberto Mioni, Luigi Bleve, Pietro Maffei, Roberto Vettor, Anna Dalla Cà, N. Xamin, Jenni Turra, Sara Azzolini
To differentiate the impact of insulin levels/resistance per se from that of excess weight on blood pressure (BP) daily changes, we evaluated, using 24-h ambulatory blood pressure monitoring (ABPM), systolic blood pressure (SBP) and diastolic blood p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb6adb5545d8e9dc832bc56d859379b
http://hdl.handle.net/11577/3218971
http://hdl.handle.net/11577/3218971
Autor:
Sara Azzolini, Caterina Luongo, Claudia Giavoli, Gianni Bona, Flavia Napoli, C. Zecchino, Laura Guazzarotti, Franco Antoniazzi, Gianluca Tornese, Luca Persani, Lorenzo Iughetti, L. Ragusa, Emiliano Zecchi, Stefano Zucchini, Stefano Stagi, Maria E. Street, Tommaso Aversa, Alberto Pietropoli
Publikováno v:
Italian Journal of Pediatrics
Background PATRO Children is an ongoing observational, longitudinal, non-interventional, global post-marketing surveillance study, which is investigating the long-term safety and effectiveness of Omnitrope®, a somatropin biosimilar to Genotropin®,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ee2faf134d8556bc00fcdd04312ffc
https://doi.org/10.1186/s13052-016-0302-3
https://doi.org/10.1186/s13052-016-0302-3
Autor:
Margherita Nosadini, Nella Augusta Greggio, Stefano Sartori, Agnese Suppiej, Sara Azzolini, Rodica Mardari, Marta Balzarin, Irene Toldo
Introduction: Allan–Herndon–Dudley syndrome is an X-linked condition caused by mutations of the monocarboxylate transporter 8 gene. This syndrome is characterized by axial hypotonia, severe mental retardation, dysarthria, athetoid movements, spas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4abefaba01b86336bc7b20b81600207a
http://hdl.handle.net/11392/2387945
http://hdl.handle.net/11392/2387945