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Page 1
Anthropometric characteristics of newborns with Prader-Willi syndrome.
Salvatoni A, Moretti A, Grugni G, Agosti M, Azzolini S, Bonaita V, Cianci P, Corica D, Crinò A, Delvecchio M, Ferraris S, Greggio NA, Iughetti L, Licenziati MR, Madeo SF, Nosetti L, Pajno R, Rutigliano I, Sacco M, Salvatore S, Scarano E, Trifirò G, Wasniewska M. Salvatoni A, et al. Among authors: rutigliano i. Am J Med Genet A. 2019 Oct;179(10):2067-2074. doi: 10.1002/ajmg.a.61304. Epub 2019 Jul 30. Am J Med Genet A. 2019. PMID: 31361394
Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment.
Palmieri VV, Lonero A, Bocchini S, Cassano G, Convertino A, Corica D, Crinò A, Fattorusso V, Ferraris S, Fintini D, Franzese A, Grugni G, Iughetti L, Lia R, Macchi F, Madeo SF, Matarazzo P, Nosetti L, Osimani S, Pajno R, Patti G, Pellegrin MC, Perri A, Ragusa L, Rutigliano I, Sacco M, Salvatoni A, Scarano E, Stagi S, Tornese G, Trifirò G, Wasniewska M, Fischetto R, Giordano P, Licenziati MR, Delvecchio M; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology. Palmieri VV, et al. Among authors: rutigliano i. Growth Horm IGF Res. 2019 Oct-Dec;48-49:9-15. doi: 10.1016/j.ghir.2019.08.003. Epub 2019 Aug 28. Growth Horm IGF Res. 2019. PMID: 31487604
Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents' experiences through a multicentre narrative medicine research.
Ragusa L, Crinò A, Grugni G, Reale L, Fiorencis A, Licenziati MR, Faienza MF, Wasniewska M, Delvecchio M, Franzese A, Rutigliano I, Fusilli P, Corica D, Campana G, Greco D, Chiarito M, Sacco M, Toscano S, Marini MG. Ragusa L, et al. Among authors: rutigliano i. BMJ Open. 2020 Aug 6;10(8):e036502. doi: 10.1136/bmjopen-2019-036502. BMJ Open. 2020. PMID: 32764084 Free PMC article.
EEG Patterns in Patients with Prader-Willi Syndrome.
Elia M, Rutigliano I, Sacco M, Madeo SF, Wasniewska M, Li Pomi A, Trifirò G, Di Bella P, De Lucia S, Vetri L, Iughetti L, Delvecchio M. Elia M, et al. Among authors: rutigliano i. Brain Sci. 2021 Aug 6;11(8):1045. doi: 10.3390/brainsci11081045. Brain Sci. 2021. PMID: 34439664 Free PMC article.
Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients.
Zucchini S, Di Iorgi N, Pozzobon G, Pedicelli S, Parpagnoli M, Driul D, Matarazzo P, Baronio F, Crocco M, Iudica G, Partenope C, Nardini B, Ubertini G, Menardi R, Guzzetti C, Iughetti L, Aversa T, Di Mase R, Cassio A; Physiopathology of Growth Processes and Puberty Study Group of the Italian Society for Pediatric Endocrinology and Diabetology. Zucchini S, et al. J Clin Endocrinol Metab. 2022 Feb 17;107(3):e1020-e1031. doi: 10.1210/clinem/dgab784. J Clin Endocrinol Metab. 2022. PMID: 34718649
Multicentric Italian case-control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome.
Panfili FM, Convertino A, Grugni G, Mazzitelli L, Bocchini S, Crinò A, Campana G, Cappa M, Delvecchio M, Faienza MF, Licenziati MR, Mariani M, Osimani S, Pajno R, Patti G, Rutigliano I, Sacco M, Scarano E, Fintini D; on behalf of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Panfili FM, et al. Among authors: rutigliano i. J Endocrinol Invest. 2023 Jul;46(7):1397-1406. doi: 10.1007/s40618-022-01990-5. Epub 2023 Jan 28. J Endocrinol Invest. 2023. PMID: 36708456
The Italian registry for patients with Prader-Willi syndrome.
Salvatore M, Torreri P, Grugni G, Rocchetti A, Maghnie M, Patti G, Crinò A, Elia M, Greco D, Romano C, Franzese A, Mozzillo E, Colao A, Pugliese G, Pagotto U, Lo Preiato V, Scarano E, Schiavariello C, Tornese G, Fintini D, Bocchini S, Osimani S, De Sanctis L, Sacco M, Rutigliano I, Delvecchio M, Faienza MF, Wasniewska M, Corica D, Stagi S, Guazzarotti L, Maffei P, Dassie F, Taruscio D. Salvatore M, et al. Among authors: rutigliano i. Orphanet J Rare Dis. 2023 Feb 15;18(1):28. doi: 10.1186/s13023-023-02633-5. Orphanet J Rare Dis. 2023. PMID: 36793093 Free PMC article.
Iodine deficiency among Italian children and adolescents assessed through 24-hour urinary iodine excretion.
Campanozzi A, Rutigliano I, Macchia PE, De Filippo G, Barbato A, Iacone R, Russo O, D'Angelo G, Frigeri M, Pensabene L, Malamisura B, Cecere G, Micillo M, Francavilla R, Tetro A, Lombardi G, Tonelli L, Castellucci G, Ferraro L, Di Biase R, Lezo A, Salvatore S, Paoletti S, Siani A, Galeone D, Formisano P, Strazzullo P. Campanozzi A, et al. Among authors: rutigliano i. Am J Clin Nutr. 2019 Apr 1;109(4):1080-1087. doi: 10.1093/ajcn/nqy393. Am J Clin Nutr. 2019. PMID: 30982855 Free article.
Diabetic ketoacidosis at the onset of disease during a national awareness campaign: a 2-year observational study in children aged 0-18 years.
Rabbone I, Maltoni G, Tinti D, Zucchini S, Cherubini V, Bonfanti R, Scaramuzza A; Diabetes Study Group of the Italian Society for Pediatric Endocrinology and Diabetology (ISPED). Rabbone I, et al. Arch Dis Child. 2020 Apr;105(4):363-366. doi: 10.1136/archdischild-2019-316903. Epub 2019 Oct 9. Arch Dis Child. 2020. PMID: 31597646 Free article.
49 results