De Mello MP - Search Results

1

A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.

Esquiaveto-Aun AM, De Mello MP, Paulino MF, Minicucci WJ, Guerra-Júnior G, De Lemos-Marini SH. Esquiaveto-Aun AM, et al. Among authors: de lemos marini sh, de mello mp. Diabetol Metab Syndr. 2015 Nov 18;7:101. doi: 10.1186/s13098-015-0101-9. eCollection 2015. Diabetol Metab Syndr. 2015. PMID: 26587058 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. Among authors: de mello mp. Am J Med Genet. 1991 Dec 15;41(4):444-5. doi: 10.1002/ajmg.1320410412. Am J Med Genet. 1991. PMID: 1776634

3

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. Among authors: de mello mp. 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

4

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. Among authors: de lemos marini sh, de mello mp. J Bone Miner Metab. 2003;21(6):396-401. doi: 10.1007/s00774-003-0434-6. J Bone Miner Metab. 2003. PMID: 14586796

5

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. Among authors: de mello mp. 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

6

Inhibition of CYP21A2 enzyme activity caused by novel missense mutations identified in Brazilian and Scandinavian patients.

Soardi FC, Barbaro M, Lau IF, Lemos-Marini SH, Baptista MT, Guerra-Junior G, Wedell A, Lajic S, de Mello MP. Soardi FC, et al. Among authors: de mello mp. J Clin Endocrinol Metab. 2008 Jun;93(6):2416-20. doi: 10.1210/jc.2007-2594. Epub 2008 Apr 1. J Clin Endocrinol Metab. 2008. PMID: 18381579

7

Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency.

Guerra-Junior G, Grumach AS, de Lemos-Marini SH, Kirschfink M, Condino Neto A, de Araujo M, De Mello MP. Guerra-Junior G, et al. Among authors: de lemos marini sh, de araujo m, de mello mp. Clin Exp Immunol. 2009 Feb;155(2):182-8. doi: 10.1111/j.1365-2249.2008.03838.x. Clin Exp Immunol. 2009. PMID: 19137635 Free PMC article.

8

Impairment in anthropometric parameters and body composition in females with classical 21-hydroxylase deficiency.

Gonçalves EM, de Lemos-Marini SH, de Mello MP, Baptista MT, D'Souza-Li LF, Baldin AD, Carvalho WR, Farias ES, Guerra-Junior G. Gonçalves EM, et al. Among authors: de lemos marini sh, de mello mp. J Pediatr Endocrinol Metab. 2009 Jun;22(6):519-29. doi: 10.1515/jpem.2009.22.6.519. J Pediatr Endocrinol Metab. 2009. PMID: 19694199

9

[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. Among authors: de mello mp. Arq Bras Endocrinol Metabol. 2009 Dec;53(9):1137-42. doi: 10.1590/s0004-27302009000900010. Arq Bras Endocrinol Metabol. 2009. PMID: 20126871 Portuguese.

10

Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency.

Coeli FB, Soardi FC, Bernardi RD, de Araújo M, Paulino LC, Lau IF, Petroli RJ, de Lemos-Marini SH, Baptista MT, Guerra-Júnior G, de-Mello MP. Coeli FB, et al. Among authors: de lemos marini sh, de araujo m, de mello mp. BMC Med Genet. 2010 Jun 29;11:104. doi: 10.1186/1471-2350-11-104. BMC Med Genet. 2010. PMID: 20587039 Free PMC article.

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