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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2012 1
2013 1
2014 1
2016 2
2017 1
2018 2
2019 3
2020 6
2021 4
2022 8
2023 4
2024 0

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29 results

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Page 1
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 Requirements in Pediatrics: From Fetal Life to Adolescence.
Iannuzzo G, Campanozzi A, Trevisani V, Rutigliano I, Abate V, Rendina D, De Filippo G. Iannuzzo G, et al. Among authors: rutigliano i. Front Endocrinol (Lausanne). 2022 Jul 1;13:929176. doi: 10.3389/fendo.2022.929176. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35846277 Free PMC article. Review.
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.
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
The Silent Epidemic of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes in Children and Adolescents in Italy During the COVID-19 Pandemic in 2020.
Cherubini V, Marino M, Scaramuzza AE, Tiberi V, Bobbio A, Delvecchio M, Piccinno E, Ortolani F, Innaurato S, Felappi B, Gallo F, Ripoli C, Ricciardi MR, Pascarella F, Stamati FA, Citriniti F, Arnaldi C, Monti S, Graziani V, De Berardinis F, Giannini C, Chiarelli F, Zampolli M, De Marco R, Bracciolini GP, Grosso C, De Donno V, Piccini B, Toni S, Coccioli S, Cardinale G, Bassi M, Minuto N, D'Annunzio G, Maffeis C, Marigliano M, Zanfardino A, Iafusco D, Rollato AS, Piscopo A, Curto S, Lombardo F, Bombaci B, Sordelli S, Mameli C, Macedoni M, Rigamonti A, Bonfanti R, Frontino G, Predieri B, Bruzzi P, Mozzillo E, Rosanio F, Franzese A, Piredda G, Cardella F, Iovane B, Calcaterra V, Berioli MG, Lasagni A, Pampanini V, Patera PI, Schiaffini R, Rutigliano I, Meloni G, De Sanctis L, Tinti D, Trada M, Guerraggio LP, Franceschi R, Cauvin V, Tornese G, Franco F, Musolino G, Maltoni G, Talarico V, Iannilli A, Lenzi L, Matteoli MC, Pozzi E, Moretti C, Zucchini S, Rabbone I, Gesuita R. Cherubini V, et al. Among authors: rutigliano i. Front Endocrinol (Lausanne). 2022 Jun 17;13:878634. doi: 10.3389/fendo.2022.878634. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35784550 Free PMC article.
29 results