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The phenotypic spectrum associated with OTX2 mutations in humans.
Gregory LC, Gergics P, Nakaguma M, Bando H, Patti G, McCabe MJ, Fang Q, Ma Q, Ozel AB, Li JZ, Poina MM, Jorge AAL, Benedetti AFF, Lerario AM, Arnhold IJP, Mendonca BB, Maghnie M, Camper SA, Carvalho LRS, Dattani MT. Gregory LC, et al. Among authors: patti g. Eur J Endocrinol. 2021 May 25;185(1):121-135. doi: 10.1530/EJE-20-1453. Eur J Endocrinol. 2021. PMID: 33950863 Free PMC article.
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: patti g. 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.
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: patti g. 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. 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.
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene.
Patti G, Scianguetta S, Roberti D, Di Mascio A, Balsamo A, Brugnara M, Cappa M, Casale M, Cavarzere P, Cipriani S, Corbetta S, Gaudino R, Iughetti L, Martini L, Napoli F, Peri A, Salerno MC, Salerno R, Passeri E, Maghnie M, Perrotta S, Di Iorgi N. Patti G, et al. Eur J Endocrinol. 2019 Sep;181(3):233-244. doi: 10.1530/EJE-19-0299. Eur J Endocrinol. 2019. PMID: 31238300 Free article.
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: patti g. Pediatr Res. 2020 Feb;87(3):456-462. doi: 10.1038/s41390-019-0487-4. Epub 2019 Jul 2. Pediatr Res. 2020. PMID: 31266054
Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency.
Patti G, Noli S, Capalbo D, Allegri AME, Napoli F, Cappa M, Ubertini GM, Gallizia A, Notarnicola S, Ibba A, Crocco M, Parodi S, Salerno M, Loche S, Garré ML, Tornari E, Maghnie M, Di Iorgi N. Patti G, et al. Front Endocrinol (Lausanne). 2019 Jul 31;10:525. doi: 10.3389/fendo.2019.00525. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31417499 Free PMC article.
585 results