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

Year Number of Results
1988 1
1989 2
1995 1
1996 1
1997 1
1998 3
1999 1
2000 2
2001 4
2002 1
2003 1
2004 3
2005 2
2006 2
2007 3
2008 1
2009 2
2010 2
2011 7
2012 5
2013 5
2014 4
2015 4
2016 4
2017 10
2018 4
2019 7
2020 8
2021 8
2022 3
2023 9
2024 7
2025 1

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103 results

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Page 1
Male Hypogonadism and Disorders of Sex Development.
Grinspon RP, Bergadá I, Rey RA. Grinspon RP, et al. Among authors: bergada i. Front Endocrinol (Lausanne). 2020 Apr 15;11:211. doi: 10.3389/fendo.2020.00211. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32351452 Free PMC article. Review.
International Guidelines for the Diagnosis and Management of Hyperinsulinism.
De Leon DD, Arnoux JB, Banerjee I, Bergada I, Bhatti T, Conwell LS, Fu J, Flanagan SE, Gillis D, Meissner T, Mohnike K, Pasquini TLS, Shah P, Stanley CA, Vella A, Yorifuji T, Thornton PS. De Leon DD, et al. Among authors: bergada i. Horm Res Paediatr. 2024;97(3):279-298. doi: 10.1159/000531766. Epub 2023 Jul 14. Horm Res Paediatr. 2024. PMID: 37454648 Free PMC article.
Are Klinefelter boys hypogonadal?
Rey RA, Gottlieb S, Pasqualini T, Bastida MG, Grinspon RP, Campo SM, Bergadá I. Rey RA, et al. Among authors: bergada i. Acta Paediatr. 2011 Jun;100(6):830-8. doi: 10.1111/j.1651-2227.2010.02137.x. Epub 2011 Feb 3. Acta Paediatr. 2011. PMID: 21214886 Review.
Disorders of Sex Development of Adrenal Origin.
Finkielstain GP, Vieites A, Bergadá I, Rey RA. Finkielstain GP, et al. Among authors: bergada i. Front Endocrinol (Lausanne). 2021 Dec 20;12:770782. doi: 10.3389/fendo.2021.770782. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34987475 Free PMC article. Review.
CDKN1C mutations: two sides of the same coin.
Eggermann T, Binder G, Brioude F, Maher ER, Lapunzina P, Cubellis MV, Bergadá I, Prawitt D, Begemann M. Eggermann T, et al. Among authors: bergada i. Trends Mol Med. 2014 Nov;20(11):614-22. doi: 10.1016/j.molmed.2014.09.001. Epub 2014 Sep 25. Trends Mol Med. 2014. PMID: 25262539 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: bergada i. J Clin Endocrinol Metab. 2024 Nov 18;109(12):3196-3210. doi: 10.1210/clinem/dgae320. J Clin Endocrinol Metab. 2024. PMID: 38717911
In Memoriam: Juan Jorge Heinrich, MD, PhD (1937-2016).
Bergadá I, Rey R. Bergadá I, et al. Pediatr Endocrinol Rev. 2017 Mar;14(3):273. doi: 10.17458/per.vol14.2017.RR.IM.heinrich. Pediatr Endocrinol Rev. 2017. PMID: 28508596 No abstract available.
Spreading the clinical window for diagnosing fetal-onset hypogonadism in boys.
Grinspon RP, Loreti N, Braslavsky D, Valeri C, Schteingart H, Ballerini MG, Bedecarrás P, Ambao V, Gottlieb S, Ropelato MG, Bergadá I, Campo SM, Rey RA. Grinspon RP, et al. Among authors: bergada i. Front Endocrinol (Lausanne). 2014 May 7;5:51. doi: 10.3389/fendo.2014.00051. eCollection 2014. Front Endocrinol (Lausanne). 2014. PMID: 24847309 Free PMC article. Review.
103 results