Maciel-Guerra AT - Search Results

1

A Search for Disorders of Sex Development among Infertile Men.

Yabiku RS, Guaragna MS, de Sousa LM, Fabbri-Scallet H, Mazzola TN, Piveta CSC, de Souza ML, Guerra-Júnior G, de Mello MP, Maciel-Guerra AT. Yabiku RS, et al. Sex Dev. 2018;12(6):275-280. doi: 10.1159/000493877. Epub 2018 Oct 30. Sex Dev. 2018. PMID: 30372699

2

True hermaphrodites in the southeastern region of Brazil: a different cytogenetic and gonadal profile.

Guerra Júnior G, de Mello MP, Assumpção JG, Morcillo AM, Marini SH, Baptista MT, Paiva e Silva RB, Marqués-de-Faria AP, Maciel-Guerra AT. Guerra Júnior G, et al. J Pediatr Endocrinol Metab. 1998 Jul-Aug;11(4):519-24. doi: 10.1515/jpem.1998.11.4.519. J Pediatr Endocrinol Metab. 1998. PMID: 9777572

3

The role of the pediatrician in the management of children with genital ambiguities.

Guerra-Júnior G, Maciel-Guerra AT. Guerra-Júnior G, et al. J Pediatr (Rio J). 2007 Nov;83(5 Suppl):S184-91. doi: 10.2223/JPED.1706. Epub 2007 Nov 1. J Pediatr (Rio J). 2007. PMID: 17973056 Review.

4

XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.

Maciel-Guerra AT, de Mello MP, Coeli FB, Ribeiro ML, Miranda ML, Marques-de-Faria AP, Baptista MT, Moraes SG, Guerra-Júnior G. Maciel-Guerra AT, et al. J Clin Endocrinol Metab. 2008 Feb;93(2):339-43. doi: 10.1210/jc.2007-1115. Epub 2007 Dec 4. J Clin Endocrinol Metab. 2008. PMID: 18056774

5

Clinical and genetic findings of five patients with WT1-related disorders.

Andrade JG, Guaragna MS, Soardi FC, Guerra-Júnior G, Mello MP, Maciel-Guerra AT. Andrade JG, et al. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1236-43. doi: 10.1590/s0004-27302008000800006. Arq Bras Endocrinol Metabol. 2008. PMID: 19169475

6

[The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome].

Barros BA, Maciel-Guerra AT, De Mello MP, Coeli FB, Carvalho AB, Viguetti-Campos N, Assumpção Jde G, Marques-de-Faria AP, Lemos-Marini SH, Guerra-Junior G. Barros BA, et al. Arq Bras Endocrinol Metabol. 2009 Dec;53(9):1137-42. doi: 10.1590/s0004-27302009000900010. Arq Bras Endocrinol Metabol. 2009. PMID: 20126871 Portuguese.

7

Complete XY gonadal dysgenesis due to p.D293N homozygous mutation in the NR5A1 gene: a case study.

Soardi FC, Coeli FB, Maciel-Guerra AT, Guerra-Júnior G, Mello MP. Soardi FC, et al. J Appl Genet. 2010;51(2):223-4. doi: 10.1007/BF03195733. J Appl Genet. 2010. PMID: 20453312

8

46,XY and 45,X/46,XY testicular dysgenesis: similar gonadal and genital phenotype, different prognosis.

Andrade JG, Guerra-Júnior G, Maciel-Guerra AT. Andrade JG, et al. Arq Bras Endocrinol Metabol. 2010 Mar;54(3):331-4. doi: 10.1590/s0004-27302010000300013. Arq Bras Endocrinol Metabol. 2010. PMID: 20520965

9

The novel p.E89K mutation in the SRY gene inhibits DNA binding and causes the 46,XY disorder of sex development.

Cunha JL, Soardi FC, Bernardi RD, Oliveira LE, Benedetti CE, Guerra-Junior G, Maciel-Guerra AT, de Mello MP. Cunha JL, et al. Braz J Med Biol Res. 2011 Apr;44(4):361-5. doi: 10.1590/s0100-879x2011007500017. Epub 2011 Feb 11. Braz J Med Biol Res. 2011. PMID: 21344134 Free article.

10

Severe forms of partial androgen insensitivity syndrome due to p.L830F novel mutation in androgen receptor gene in a Brazilian family.

Petroli RJ, Maciel-Guerra AT, Soardi FC, de Calais FL, Guerra-Junior G, de Mello MP. Petroli RJ, et al. BMC Res Notes. 2011 Jun 6;4:173. doi: 10.1186/1756-0500-4-173. BMC Res Notes. 2011. PMID: 21645389 Free PMC article.

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