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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: greggio na. 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
Cystic fibrosis genetics in southern Europe.
Anglani F, Camporese C, Picci L, Greggio NA, Barbato A, Zacchello F. Anglani F, et al. Among authors: greggio na. Lancet. 1990 Aug 11;336(8711):379-80. doi: 10.1016/0140-6736(90)91925-z. Lancet. 1990. PMID: 1975362 No abstract available.
Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia.
Karlsson L, de Paula Michelatto D, Lusa ALG, D'Almeida Mgnani Silva C, Östberg LJ, Persson B, Guerra-Júnior G, Valente de Lemos-Marini SH, Baldazzi L, Menabó S, Balsamo A, Greggio NA, Palandi de Mello M, Barbaro M, Lajic S. Karlsson L, et al. Among authors: greggio na. Clin Biochem. 2019 Nov;73:50-56. doi: 10.1016/j.clinbiochem.2019.07.009. Epub 2019 Jul 22. Clin Biochem. 2019. PMID: 31344365
Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients.
Iughetti L, Vivi G, Balsamo A, Corrias A, Crinò A, Delvecchio M, Gargantini L, Greggio NA, Grugni G, Hladnik U, Pilotta A, Ragusa L, Salvatoni A, Wasniewska M, Weber G, Predieri B. Iughetti L, et al. Among authors: greggio na. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):159-165. doi: 10.1515/jpem-2018-0388. J Pediatr Endocrinol Metab. 2019. PMID: 30703060
47 results