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

Year Number of Results
1981 1
1982 2
1983 2
1985 1
1986 2
1987 5
1988 2
1989 3
1990 1
1991 1
1992 3
1993 3
1995 3
1996 3
1997 2
1998 1
1999 4
2000 2
2001 3
2002 4
2003 4
2005 1
2006 6
2007 7
2008 2
2009 5
2010 6
2011 3
2012 4
2013 5
2014 5
2015 6
2016 4
2017 6
2018 8
2019 6
2020 3
2021 7
2022 5
2023 1
2024 3
2025 4

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137 results

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Page 1
Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome.
Marino R, Moresco A, Perez Garrido N, Ramirez P, Belgorosky A. Marino R, et al. Among authors: belgorosky a. Front Endocrinol (Lausanne). 2022 Feb 25;13:803226. doi: 10.3389/fendo.2022.803226. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35282436 Free PMC article. Review.
Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes.
Martinez-Mayer J, Vishnopolska S, Perticarari C, Iglesias Garcia L, Hackbartt M, Martinez M, Zaiat J, Jacome-Alvarado A, Braslavsky D, Keselman A, Bergadá I, Marino R, Ramírez P, Pérez Garrido N, Ciaccio M, Di Palma MI, Belgorosky A, Forclaz MV, Benzrihen G, D'Amato S, Cirigliano ML, Miras M, Paez Nuñez A, Castro L, Mallea-Gil MS, Ballarino C, Latorre-Villacorta L, Casiello AC, Hernandez C, Figueroa V, Alonso G, Morin A, Guntsche Z, Lee H, Lee E, Song Y, Marti MA, Perez-Millan MI. Martinez-Mayer J, et al. Among authors: belgorosky a. J Clin Endocrinol Metab. 2024 Nov 18;109(12):3196-3210. doi: 10.1210/clinem/dgae320. J Clin Endocrinol Metab. 2024. PMID: 38717911
Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone.
Baquedano MS, Guercio G, Costanzo M, Marino R, Rivarola MA, Belgorosky A. Baquedano MS, et al. Among authors: belgorosky a. Vitam Horm. 2018;108:75-123. doi: 10.1016/bs.vh.2018.05.002. Epub 2018 Jun 30. Vitam Horm. 2018. PMID: 30029738 Review.
A Surgical and Clinical Approach to Persistent Müllerian Duct Syndrome: Laparoscopic, Histological, and Molecular Findings.
Mattone MC, Lobo de la Vega MV, Redondo EJ, D'Alessandro P, Perez Garrido N, Galluzzo ML, Costanzo M, Zaidman V, Lazzati JM, Berensztein E, Ramirez P, Marino R, Belgorosky A, Ciaccio M, Bailez M, Guercio G. Mattone MC, et al. Among authors: belgorosky a. Sex Dev. 2023;17(1):1-7. doi: 10.1159/000526992. Epub 2023 Jan 10. Sex Dev. 2023. PMID: 36626890
Preserved fertility in a patient with a 46,XY disorder of sex development due to a new heterozygous mutation in the NR5A1/SF-1 gene: evidence of 46,XY and 46,XX gonadal dysgenesis phenotype variability in multiple members of an affected kindred.
Ciaccio M, Costanzo M, Guercio G, De Dona V, Marino R, Ramirez PC, Galeano J, Warman DM, Berensztein E, Saraco N, Baquedano MS, Chaler E, Maceiras M, Lazzatti JM, Rivarola MA, Belgorosky A. Ciaccio M, et al. Among authors: belgorosky a. Horm Res Paediatr. 2012;78(2):119-26. doi: 10.1159/000338346. Epub 2012 Aug 14. Horm Res Paediatr. 2012. PMID: 22907560 Clinical Trial.
137 results