Marques-de-Faria AP - Search Results

1

Why pediatricians need to know the disorders of sex development: experience of 709 cases in a specialized service.

Beck MSE, Germano CW, Barros BA, Andrade JGR, Guaragna-Filho G, Paula GB, Miranda ML, Guaragna MS, Fabbri-Scallet H, Mazzola TN, Viguetti-Campos NL, Vieira TAP, Lemos-Marini SHV, Marques-de-Faria AP, Silva RBPE, Mello MP, Maciel-Guerra AT, Guerra-Júnior G. Beck MSE, et al. Among authors: marques de faria ap. J Pediatr (Rio J). 2020 Sep-Oct;96(5):607-613. doi: 10.1016/j.jped.2019.04.007. Epub 2019 Jun 27. J Pediatr (Rio J). 2020. PMID: 31254527 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

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

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

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

7

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

8

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

9

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

10

[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.

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