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Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review.
Garavelli L, Cerruti-Mainardi P, Virdis R, Pedori S, Pastore G, Godi M, Provera S, Rauch A, Zweier C, Zollino M, Banchini G, Longo N, Mowat D, Neri G, Bernasconi S. Garavelli L, et al. Among authors: pedori s. Horm Res. 2005;63(4):187-92. doi: 10.1159/000085894. Epub 2005 May 20. Horm Res. 2005. PMID: 15908750
Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosis.
Guareschi E, Garavelli L, Pedori S, Di Lernia V, Grenzi L, Franchi F, Marinelli M, Croci GF, Pedretti E, Amarri S, Banchini G, Albertini G. Guareschi E, et al. Among authors: pedori s. Pediatr Dermatol. 2007 Jul-Aug;24(4):426-8. doi: 10.1111/j.1525-1470.2007.00469.x. Pediatr Dermatol. 2007. PMID: 17845177 No abstract available.
Multiple sulfatase deficiency with neonatal manifestation.
Garavelli L, Santoro L, Iori A, Gargano G, Braibanti S, Pedori S, Melli N, Frattini D, Zampini L, Galeazzi T, Padella L, Pepe S, Wischmeijer A, Rosato S, Ivanovski I, Iughetti L, Gelmini C, Bernasconi S, Superti-Furga A, Ballabio A, Gabrielli O. Garavelli L, et al. Among authors: pedori s. Ital J Pediatr. 2014 Dec 17;40:86. doi: 10.1186/s13052-014-0086-2. Ital J Pediatr. 2014. PMID: 25516103 Free PMC article.
Reduced prevalence of fetal exposure to alcohol in Italy: a nationwide survey.
La Maida N, Di Giorgi A, Pellegrini M, Ceccanti M, Caruso S, Ricci G, Neri I, Lana S, Minutillo A, Berretta P, Busardò FP, Pichini S; CCM Study Group. La Maida N, et al. Am J Obstet Gynecol MFM. 2023 Jun;5(6):100944. doi: 10.1016/j.ajogmf.2023.100944. Epub 2023 Mar 25. Am J Obstet Gynecol MFM. 2023. PMID: 36972834 No abstract available.
13 results