Montenegro L - Search Results

1

Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations.

Seraphim CE, Canton APM, Montenegro L, Piovesan MR, Macedo DB, Cunha M, Guimaraes A, Ramos CO, Benedetti AFF, de Castro Leal A, Gagliardi PC, Antonini SR, Gryngarten M, Arcari AJ, Abreu AP, Kaiser UB, Soriano-Guillén L, Escribano-Muñoz A, Corripio R, Labarta JI, Travieso-Suárez L, Ortiz-Cabrera NV, Argente J, Mendonca BB, Brito VN, Latronico AC. Seraphim CE, et al. Among authors: montenegro l. J Clin Endocrinol Metab. 2021 Mar 25;106(4):1041-1050. doi: 10.1210/clinem/dgaa955. J Clin Endocrinol Metab. 2021. PMID: 33383582 Free PMC article.

2

Growth hormone (GH) pharmacogenetics: influence of GH receptor exon 3 retention or deletion on first-year growth response and final height in patients with severe GH deficiency.

Jorge AA, Marchisotti FG, Montenegro LR, Carvalho LR, Mendonca BB, Arnhold IJ. Jorge AA, et al. Among authors: montenegro lr. J Clin Endocrinol Metab. 2006 Mar;91(3):1076-80. doi: 10.1210/jc.2005-2005. Epub 2005 Nov 15. J Clin Endocrinol Metab. 2006. PMID: 16291702

3

[Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation].

Ferreira LV, Souza SA, Montenegro LR, Arnhold IJ, Pasqualini T, Heinrich JJ, Keselman AC, Mendonça BB, Jorge AA. Ferreira LV, et al. Among authors: montenegro lr. Arq Bras Endocrinol Metabol. 2007 Apr;51(3):450-6. doi: 10.1590/s0004-27302007000300014. Arq Bras Endocrinol Metabol. 2007. PMID: 17546245 Portuguese.

4

Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients.

Ferreira LV, Souza SC, Montenegro LR, Malaquias AC, Arnhold IJ, Mendonca BB, Jorge AA. Ferreira LV, et al. Among authors: montenegro lr. Clin Endocrinol (Oxf). 2008 Sep;69(3):426-31. doi: 10.1111/j.1365-2265.2008.03234.x. Epub 2008 Mar 10. Clin Endocrinol (Oxf). 2008. PMID: 18331608

5

Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant.

Marchisotti FG, Jorge AA, Montenegro LR, Berger K, de Carvalho LR, Mendonca BB, Arnhold IJ. Marchisotti FG, et al. Growth Horm IGF Res. 2009 Apr;19(2):179-86. doi: 10.1016/j.ghir.2008.10.001. Epub 2008 Nov 25. Growth Horm IGF Res. 2009. PMID: 19036620

6

Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver-Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11.

Montenegro LR, Leal AC, Coutinho DC, Valassi HP, Nishi MY, Arnhold IJ, Mendonca BB, Jorge AA. Montenegro LR, et al. Eur J Endocrinol. 2012 Mar;166(3):543-50. doi: 10.1530/EJE-11-0964. Epub 2011 Dec 14. Eur J Endocrinol. 2012. PMID: 22170793 Free article.

7

[Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism].

Tusset C, Trarbach EB, Silveira LF, Beneduzzi D, Montenegro L, Latronico AC. Tusset C, et al. Among authors: montenegro l. Arq Bras Endocrinol Metabol. 2011 Nov;55(8):501-11. doi: 10.1590/s0004-27302011000800002. Arq Bras Endocrinol Metabol. 2011. PMID: 22218430 Review. Portuguese.

8

[Mutations in insulin-like growth factor receptor 1 gene (IGF1R) resulting in intrauterine and postnatal growth retardation].

Leal Ade C, Canton AP, Montenegro LR, Coutinho DC, Arnhold IJ, Jorge AA. Leal Ade C, et al. Arq Bras Endocrinol Metabol. 2011 Nov;55(8):541-9. doi: 10.1590/s0004-27302011000800007. Arq Bras Endocrinol Metabol. 2011. PMID: 22218435 Review. Portuguese.

9

The interactive effect of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndrome.

Braz AF, Costalonga EF, Montenegro LR, Trarbach EB, Antonini SR, Malaquias AC, Ramos ES, Mendonca BB, Arnhold IJ, Jorge AA. Braz AF, et al. Among authors: montenegro lr. J Clin Endocrinol Metab. 2012 Apr;97(4):E671-7. doi: 10.1210/jc.2011-2521. Epub 2012 Jan 25. J Clin Endocrinol Metab. 2012. PMID: 22278433 Free article.

10

Analysis of the insulin-like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p.Arg511Trp).

Leal AC, Montenegro LR, Saito RF, Ribeiro TC, Coutinho DC, Mendonca BB, Arnhold IJ, Jorge AA. Leal AC, et al. Among authors: montenegro lr. Clin Endocrinol (Oxf). 2013 Apr;78(4):558-63. doi: 10.1111/cen.12048. Clin Endocrinol (Oxf). 2013. PMID: 22998174

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