Guerra-Júnior G - Search Results

1

Pharmacogenetics of Risperidone and Cardiovascular Risk in Children and Adolescents.

Dos Santos-Júnior A, Henriques TB, de Mello MP, Della Torre OH, Paes LA, Ferreira-Neto AP, Sewaybricker LE, Fontana TS, Celeri EH, Guerra-Júnior G, Dalgalarrondo P. Dos Santos-Júnior A, et al. Int J Endocrinol. 2016;2016:5872423. doi: 10.1155/2016/5872423. Epub 2016 Jan 6. Int J Endocrinol. 2016. PMID: 26880915 Free PMC article.

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

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

4

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. 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

5

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. 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.

6

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. 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

7

[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.

8

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.

9

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.

10

Normalization of height and excess body fat in children with salt-wasting 21-hydroxylase deficiency.

Mendes-Dos-Santos CT, Lemos-Marini SH, Baptista MT, Guerra-Junior G, De-Mello MP, Paulino MF, Morcillo AM. Mendes-Dos-Santos CT, et al. J Pediatr (Rio J). 2011 May-Jun 8;87(3):263-8. doi: 10.2223/JPED.2095. J Pediatr (Rio J). 2011. PMID: 21660369 English, Portuguese.

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