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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
2005 2
2007 4
2008 3
2009 1
2010 5
2011 8
2012 8
2013 1
2014 3
2015 2
2016 3
2017 4
2018 5
2019 2
2020 3
2021 1
2022 5
2023 4
2024 1

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60 results

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Page 1
DHX37 and the implications in Disorders of Sex Development: an update review.
de Oliveira FR, Guaragna MS, Maciel-Guerra AT, Barros BA, de Mello MP, Guerra-Junior G, Fabbri-Scallet H. de Oliveira FR, et al. Among authors: maciel guerra at. Horm Res Paediatr. 2023 Dec 23. doi: 10.1159/000535969. Online ahead of print. Horm Res Paediatr. 2023. PMID: 38142677 Review.
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.
de Oliveira FR, Mazzola TN, de Mello MP, Francese-Santos AP, Lemos-Marini SHV, Maciel-Guerra AT, Hiort O, Werner R, Guerra-Junior G, Fabbri-Scallet H. de Oliveira FR, et al. Among authors: maciel guerra at. Life (Basel). 2023 Apr 27;13(5):1093. doi: 10.3390/life13051093. Life (Basel). 2023. PMID: 37240737 Free PMC article.
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.
Riccetto L, Vieira TP, Viguetti-Campos NL, Mazzola TN, Guaragna MS, Fabbri-Scallet H, Mello MP, Marques-de-Faria AP, Maciel-Guerra AT, Guerra Junior G. Riccetto L, et al. Among authors: maciel guerra at. Sao Paulo Med J. 2022 Nov 28;141(4):e2022281. doi: 10.1590/1516-3180.2022.0281.R1.30082022. eCollection 2022. Sao Paulo Med J. 2022. PMID: 36449967 Free PMC article.
SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.
de Oliveira FM, Barros BA, Dos Santos AP, Campos NLV, Mazzola TN, Filho PL, Andrade LALA, Guaragna MS, de Mello MP, Guerra-Junior G, Vieira TAP, Maciel-Guerra AT. de Oliveira FM, et al. Among authors: maciel guerra at. Am J Med Genet A. 2023 Feb;191(2):592-598. doi: 10.1002/ajmg.a.63051. Epub 2022 Nov 23. Am J Med Genet A. 2023. PMID: 36416214
Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region.
Guaragna MS, Ledesma FL, Manzano VZ, Maciel-Guerra AT, Guerra-Júnior G, Silva MM, Luiz de Brito P, Palandi de Mello M. Guaragna MS, et al. Among authors: maciel guerra at. J Pediatr Endocrinol Metab. 2022 Mar 21;35(6):837-843. doi: 10.1515/jpem-2021-0673. Print 2022 Jun 27. J Pediatr Endocrinol Metab. 2022. PMID: 35304980
Leydig and Sertoli cell function in individuals with genital ambiguity, 46,XY karyotype, palpable gonads and normal testosterone secretion: a case-control study.
Guaragna-Filho G, Calixto AR, Astur ABLDV, Paula GB, Oliveira LC, Morcillo AM, Gonçalves EM, Mello MP, Maciel-Guerra AT, Guerra-Junior G. Guaragna-Filho G, et al. Among authors: maciel guerra at. Sao Paulo Med J. 2022 Mar-Apr;140(2):163-170. doi: 10.1590/1516-3180.2021.0042.R1.08062021. Sao Paulo Med J. 2022. PMID: 35137906 Free PMC article.
60 results