Maciel-Guerra AT - Search Results

1

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.

2

True agonadism: report of a case analyzed with Y-specific DNA probes.

Maciel-Guerra AT, Farah SB, Garmes HM, Pinto Júnior W, Bustorff da Silva JM, Baptista MT, Marques-de-Faria AP, Guerra Júnior G, de Mello MP. Maciel-Guerra AT, et al. Am J Med Genet. 1991 Dec 15;41(4):444-5. doi: 10.1002/ajmg.1320410412. Am J Med Genet. 1991. PMID: 1776634

3

Mutations of androgen receptor gene in Brazilian patients with male pseudohermaphroditism.

Cabral DF, Maciel-Guerra AT, Hackel C. Cabral DF, et al. Braz J Med Biol Res. 1998 Jun;31(6):775-8. doi: 10.1590/s0100-879x1998000600008. Braz J Med Biol Res. 1998. PMID: 9698822

4

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

5

Evaluation of the tubular and interstitial functions of the testis in 46,XY patients with ambiguous genitalia.

Stuchi-Perez EG, Lukas-Croisier C, De Castro M, Baptista MT, Ribeiro Scolfaro M, Marques-De-Faria AP, Hackel C, Maciel-Guerra AT, Guerra Júnior G. Stuchi-Perez EG, et al. J Pediatr Endocrinol Metab. 2000 Jun;13(6):605-12. doi: 10.1515/jpem.2000.13.6.605. J Pediatr Endocrinol Metab. 2000. PMID: 10905384

6

Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypes.

Assumpção JG, Benedetti CE, Maciel-Guerra AT, Guerra G Jr, Baptista MT, Scolfaro MR, de Mello MP. Assumpção JG, et al. J Mol Med (Berl). 2002 Dec;80(12):782-90. doi: 10.1007/s00109-002-0376-9. Epub 2002 Oct 1. J Mol Med (Berl). 2002. PMID: 12483463

7

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density.

de Almeida Freire PO, de Lemos-Marini SH, Maciel-Guerra AT, Morcillo AM, Matias Baptista MT, de Mello MP, Guerra G Jr. de Almeida Freire PO, et al. J Bone Miner Metab. 2003;21(6):396-401. doi: 10.1007/s00774-003-0434-6. J Bone Miner Metab. 2003. PMID: 14586796

8

Mutations in SRY and WT1 genes required for gonadal development are not responsible for XY partial gonadal dysgenesis.

Tagliarini EB, Assumpção JG, Scolfaro MR, Mello MP, Maciel-Guerra AT, Guerra Júnior G, Hackel C. Tagliarini EB, et al. Braz J Med Biol Res. 2005 Jan;38(1):17-25. doi: 10.1590/s0100-879x2005000100004. Epub 2005 Jan 18. Braz J Med Biol Res. 2005. PMID: 15665984 Free article.

9

[Evaluation of insulin resistance and lipid profile in turner syndrome].

de Armani MC, Baldin AD, Lemos-Marini SH, Baptista MT, Maciel-Guerra AT, Guerra-Junior G. de Armani MC, et al. Arq Bras Endocrinol Metabol. 2005 Apr;49(2):278-85. doi: 10.1590/s0004-27302005000200015. Epub 2005 Sep 12. Arq Bras Endocrinol Metabol. 2005. PMID: 16184257 Portuguese.

10

A naturally occurring deletion in the SRY promoter region affecting the Sp1 binding site is associated with sex reversal.

Assumpção JG, Ferraz LF, Benedetti CE, Maciel-Guerra AT, Guerra G Jr, Marques-de-Faria AP, Baptista MT, de Mello MP. Assumpção JG, et al. J Endocrinol Invest. 2005 Jul-Aug;28(7):651-6. doi: 10.1007/BF03347266. J Endocrinol Invest. 2005. PMID: 16218050

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