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Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.
Salvatore M, Polizzi A, De Stefano MC, Floridia G, Baldovino S, Roccatello D, Sciascia S, Menegatti E, Remuzzi G, Daina E, Iatropoulos P, Bembi B, Da Riol RM, Ferlini A, Neri M, Novelli G, Sangiuolo F, Brancati F, Taruscio D. Salvatore M, et al. Among authors: da riol rm. Ital J Pediatr. 2020 Sep 14;46(1):130. doi: 10.1186/s13052-020-00883-8. Ital J Pediatr. 2020. PMID: 32928283 Free PMC article.
Vitamin D deficiency in a population of migrant children: an Italian retrospective cross-sectional multicentric study.
Ceccarelli M, Chiappini E, Arancio R, Zaffaroni M, La Placa S, D'Andrea M, de Waure C, Da Riol RM, Valentini P; on the behalf of National Working Group for the Migrant Children of the Italian Society of Pediatrics (NWGMC-ISP). Ceccarelli M, et al. Among authors: da riol rm. Eur J Public Health. 2020 Jun 1;30(3):551-556. doi: 10.1093/eurpub/ckz182. Eur J Public Health. 2020. PMID: 31598638
In vitro and in vivo effects of Ambroxol chaperone therapy in two Italian patients affected by neuronopathic Gaucher disease and epilepsy.
Ciana G, Dardis A, Pavan E, Da Riol RM, Biasizzo J, Ferino D, Zanatta M, Boni A, Antonini L, Crichiutti G, Bembi B. Ciana G, et al. Among authors: da riol rm. Mol Genet Metab Rep. 2020 Nov 21;25:100678. doi: 10.1016/j.ymgmr.2020.100678. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33294373 Free PMC article.