Maciel-Guerra AT - Search Results

1

Congenital perineal lipoma presenting as ambiguous genitalia.

Guerra-Junior G, Aun AM, Miranda ML, Beraldo LP, Guimaraes Moraes S, Baptista MT, Marques-de-Faria AP, Maciel-Guerra AT. Guerra-Junior G, et al. Eur J Pediatr Surg. 2008 Aug;18(4):269-71. doi: 10.1055/s-2008-1038366. Epub 2008 Aug 14. Eur J Pediatr Surg. 2008. PMID: 18704895

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

Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome.

Maciel-Guerra AT, Guerra G Jr, Marini SH, Matias Baptista MT, Marques-de-Faria AP. Maciel-Guerra AT, et al. Clin Genet. 1997 May;51(5):351-3. doi: 10.1111/j.1399-0004.1997.tb02487.x. Clin Genet. 1997. PMID: 9212186

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

Turner's syndrome and thyroid disease: a transverse study of pediatric patients in Brazil.

Medeiros CC, Marini SH, Baptista MT, Guerra G Jr, Maciel-Guerra AT. Medeiros CC, et al. J Pediatr Endocrinol Metab. 2000 Apr;13(4):357-62. doi: 10.1515/jpem.2000.13.4.357. J Pediatr Endocrinol Metab. 2000. PMID: 10776989

6

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

7

A boy with mental retardation, blepharophimosis and hypothyroidism: a diagnostic dilemma between Young-Simpson and Ohdo syndrome.

Marques-de-faria AP, Maciel-Guerra AT, Júnior GG, Baptista MT. Marques-de-faria AP, et al. Clin Dysmorphol. 2000 Jul;9(3):199-204. doi: 10.1097/00019605-200009030-00009. Clin Dysmorphol. 2000. PMID: 10955481

8

Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patients.

Costa AM, Lemos-Marini SH, Baptista MT, Morcillo AM, Maciel-Guerra AT, Guerra G Jr. Costa AM, et al. J Bone Miner Metab. 2002;20(5):294-7. doi: 10.1007/s007740200042. J Bone Miner Metab. 2002. PMID: 12203035 Clinical Trial.

9

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

10

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.

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