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Page 1
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations.
Rigoli L, Aloi C, Salina A, Di Bella C, Salzano G, Caruso R, Mazzon E, Maghnie M, Patti G, D'Annunzio G, Lombardo F. Rigoli L, et al. Among authors: maghnie m. Pediatr Res. 2020 Feb;87(3):456-462. doi: 10.1038/s41390-019-0487-4. Epub 2019 Jul 2. Pediatr Res. 2020. PMID: 31266054
Combined therapy with insulin and growth hormone in 17 patients with type-1 diabetes and growth disorders.
Zucchini S, Iafusco D, Vannelli S, Rabbone I, Salzano G, Pozzobon G, Maghnie M, Cherubini V, Bizzarri C, Bonfanti R, D'Annunzio G, Lenzi L, Maggio MC, Marigliano M, Scaramuzza A, Tumini S, Iughetti L. Zucchini S, et al. Among authors: maghnie m. Horm Res Paediatr. 2014;82(1):53-8. doi: 10.1159/000360856. Epub 2014 Jun 11. Horm Res Paediatr. 2014. PMID: 24925520
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Perrotta S, Di Iorgi N, Ragione FD, Scianguetta S, Borriello A, Allegri AE, Ferraro M, Santoro C, Napoli F, Calcagno A, Giaccardi M, Cappa M, Salerno MC, Cozzolino D, Maghnie M. Perrotta S, et al. Among authors: maghnie m. Eur J Endocrinol. 2015 Apr;172(4):461-72. doi: 10.1530/EJE-14-0942. Eur J Endocrinol. 2015. PMID: 25740874
Classical and non-classical causes of GH deficiency in the paediatric age.
Di Iorgi N, Morana G, Allegri AE, Napoli F, Gastaldi R, Calcagno A, Patti G, Loche S, Maghnie M. Di Iorgi N, et al. Among authors: maghnie m. Best Pract Res Clin Endocrinol Metab. 2016 Dec;30(6):705-736. doi: 10.1016/j.beem.2016.11.008. Epub 2016 Nov 24. Best Pract Res Clin Endocrinol Metab. 2016. PMID: 27974186 Review.
Glucokinase mutations in pediatric patients with impaired fasting glucose.
Aloi C, Salina A, Minuto N, Tallone R, Lugani F, Mascagni A, Mazza O, Cassanello M, Maghnie M, d'Annunzio G. Aloi C, et al. Among authors: maghnie m. Acta Diabetol. 2017 Oct;54(10):913-923. doi: 10.1007/s00592-017-1021-y. Epub 2017 Jul 19. Acta Diabetol. 2017. PMID: 28726111
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases.
Godano E, Morana G, Di Iorgi N, Pistorio A, Allegri AEM, Napoli F, Gastaldi R, Calcagno A, Patti G, Gallizia A, Notarnicola S, Giaccardi M, Noli S, Severino M, Tortora D, Rossi A, Maghnie M. Godano E, et al. Among authors: maghnie m. Eur J Endocrinol. 2018 Jun;178(6):613-622. doi: 10.1530/EJE-18-0094. Epub 2018 Apr 12. Eur J Endocrinol. 2018. PMID: 29650689
Central adrenal insufficiency in children and adolescents.
Patti G, Guzzeti C, Di Iorgi N, Maria Allegri AE, Napoli F, Loche S, Maghnie M. Patti G, et al. Among authors: maghnie m. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):425-444. doi: 10.1016/j.beem.2018.03.012. Epub 2018 Apr 10. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086867 Review.
301 results