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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 1
2005 2
2006 6
2007 4
2008 1
2009 3
2010 4
2011 4
2012 4
2013 6
2014 4
2015 2
2016 8
2017 5
2018 6
2019 6
2020 8
2021 11
2022 11
2023 13
2024 4

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109 results

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Page 1
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.
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.
Spatial Beam Self-Cleaning in Second-Harmonic Generation.
Krupa K, Fona R, Tonello A, Labruyère A, Shalaby BM, Wabnitz S, Baronio F, Aceves AB, Millot G, Couderc V. Krupa K, et al. Among authors: baronio f. Sci Rep. 2020 Apr 29;10(1):7204. doi: 10.1038/s41598-020-64080-7. Sci Rep. 2020. PMID: 32350305 Free PMC article.
Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia.
Righi B, Ali SR, Bryce J, Tomlinson JW, Bonfig W, Baronio F, Costa EC, Guaragna-Filho G, T'Sjoen G, Cools M, Markosyan R, Bachega TASS, Miranda MC, Iotova V, Falhammar H, Ceccato F, Stancampiano MR, Russo G, Daniel E, Auchus RJ, Ross RJ, Ahmed SF. Righi B, et al. Among authors: baronio f. Endocrine. 2023 Jun;80(3):630-638. doi: 10.1007/s12020-023-03330-w. Epub 2023 Mar 1. Endocrine. 2023. PMID: 36857009 Free PMC article.
Two-color walking Peregrine solitary waves.
Baronio F, Chen S, Mihalache D. Baronio F, et al. Opt Lett. 2017 Sep 15;42(18):3514-3517. doi: 10.1364/OL.42.003514. Opt Lett. 2017. PMID: 28914889
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe.
Nowotny H, Neumann U, Tardy-Guidollet V, Ahmed SF, Baronio F, Battelino T, Bertherat J, Blankenstein O, Bonomi M, Bouvattier C, Brac de la Perrière A, Brucker S, Cappa M, Chanson P, Claahsen-van der Grinten HL, Colao A, Cools M, Davies JH, Dörr HG, Fenske WK, Ghigo E, Giordano R, Gravholt CH, Huebner A, Husebye ES, Igbokwe R, Juul A, Kiefer FW, Léger J, Menassa R, Meyer G, Neocleous V, Phylactou LA, Rohayem J, Russo G, Scaroni C, Touraine P, Unger N, Vojtková J, Yeste D, Lajic S, Reisch N. Nowotny H, et al. Among authors: baronio f. Eur J Endocrinol. 2022 Mar 23;186(5):K17-K24. doi: 10.1530/EJE-21-0554. Eur J Endocrinol. 2022. PMID: 35235536 Free PMC article.
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