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Editorial: Bone health and development in children and adolescents.
Baronio F, Baptista F. Baronio F, et al. Front Endocrinol (Lausanne). 2022 Dec 12;13:1101403. doi: 10.3389/fendo.2022.1101403. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36578952 Free PMC article. No abstract available.
Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation.
Tonin R, Caciotti A, Funghini S, Pasquini E, Mooney SD, Cai B, Proncopio E, Donati MA, Baronio F, Bettocchi I, Cassio A, Biasucci G, Bordugo A, la Marca G, Guerrini R, Morrone A. Tonin R, et al. Among authors: baronio f. BBA Clin. 2016 Mar 10;5:114-9. doi: 10.1016/j.bbacli.2016.03.004. eCollection 2016 Jun. BBA Clin. 2016. PMID: 27051597 Free PMC article.
Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia.
Wasniewska MG, Morabito LA, Baronio F, Einaudi S, Salerno M, Bizzarri C, Russo G, Chiarito M, Grandone A, Guazzarotti L, Spinuzza A, Corica D, Ortolano R, Balsamo A, Abrigo E, Baldini Ferroli B, Alibrandi A, Capalbo D, Aversa T, Faienza MF; Adrenal Diseases Working Group of the Italian Society for Pediatric Endocrinology and Diabetology. Wasniewska MG, et al. Among authors: baronio f. Horm Res Paediatr. 2020;93(3):173-181. doi: 10.1159/000509548. Epub 2020 Aug 18. Horm Res Paediatr. 2020. PMID: 32810858 Free article. Clinical Trial.
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.
Chien YH, Abdenur JE, Baronio F, Bannick AA, Corrales F, Couce M, Donner MG, Ficicioglu C, Freehauf C, Frithiof D, Gotway G, Hirabayashi K, Hofstede F, Hoganson G, Hwu WL, James P, Kim S, Korman SH, Lachmann R, Levy H, Lindner M, Lykopoulou L, Mayatepek E, Muntau A, Okano Y, Raymond K, Rubio-Gozalbo E, Scholl-Bürgi S, Schulze A, Singh R, Stabler S, Stuy M, Thomas J, Wagner C, Wilson WG, Wortmann S, Yamamoto S, Pao M, Blom HJ. Chien YH, et al. Among authors: baronio f. Orphanet J Rare Dis. 2015 Aug 20;10:99. doi: 10.1186/s13023-015-0321-y. Orphanet J Rare Dis. 2015. PMID: 26289392 Free PMC article. Review.
109 results