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Letter to the Editors: Concerning "Divergent clinical outcomes of alphaglucosidase enzyme replacement therapy in two siblings with infantile-onset Pompe disease treated in the symptomatic or pre-symptomatic state" by Takashi M et al.
Ortolano R, Baronio F, Masetti R, Prete A, Cassio A, Pession A. Ortolano R, et al. Among authors: baronio f. Mol Genet Metab Rep. 2017 Mar 7;11:1. doi: 10.1016/j.ymgmr.2017.02.003. eCollection 2017 Jun. Mol Genet Metab Rep. 2017. PMID: 28316933 Free PMC article. No abstract available.
Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant.
Balsamo A, Baronio F, Ortolano R, Menabo S, Baldazzi L, Di Natale V, Vissani S, Cassio A. Balsamo A, et al. Among authors: baronio f. Front Pediatr. 2020 Dec 22;8:593315. doi: 10.3389/fped.2020.593315. eCollection 2020. Front Pediatr. 2020. PMID: 33415088 Free PMC article. Review.
Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature.
Candela E, Zagariello M, Di Natale V, Ortolano R, Righetti F, Assirelli V, Biasucci G, Cassio A, Pession A, Baronio F. Candela E, et al. Among authors: baronio f. Children (Basel). 2023 Feb 17;10(2):396. doi: 10.3390/children10020396. Children (Basel). 2023. PMID: 36832525 Free PMC article.
Premature Pubarche: Time to Revise the Diagnostic Approach?
Baronio F, Marzatico A, De Iasio R, Ortolano R, Fanolla A, Radetti G, Balsamo A, Pession A, Cassio A. Baronio F, et al. J Clin Med. 2023 Mar 11;12(6):2187. doi: 10.3390/jcm12062187. J Clin Med. 2023. PMID: 36983190 Free PMC article.
109 results