Scalco R - Search Results

1

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome.

Scalco R, Trarbach E, Albuquerque EVA, Homma TK, Inoue-Lima TH, Nishi MY, Mendonca BB, Jorge AAL. Scalco R, et al. Endocr Connect. 2019 Nov;8(11):1513-1519. doi: 10.1530/EC-19-0398. Endocr Connect. 2019. PMID: 31671406 Free PMC article.

2

Effectiveness of the combined recombinant human growth hormone and gonadotropin-releasing hormone analog therapy in pubertal patients with short stature due to SHOX deficiency.

Scalco RC, Melo SS, Pugliese-Pires PN, Funari MF, Nishi MY, Arnhold IJ, Mendonca BB, Jorge AA. Scalco RC, et al. J Clin Endocrinol Metab. 2010 Jan;95(1):328-32. doi: 10.1210/jc.2009-1577. Epub 2009 Nov 19. J Clin Endocrinol Metab. 2010. PMID: 19926713 Free PMC article. Clinical Trial.

3

[STAT5B deficiency: a new growth hormone insensitivity syndrome associated to immunological dysfunction].

Scalco RC, Pugliese-Pires PN, Jorge AA. Scalco RC, et al. Arq Bras Endocrinol Metabol. 2013 Jul;57(5):333-8. doi: 10.1590/s0004-27302013000500001. Arq Bras Endocrinol Metabol. 2013. PMID: 23896798 Review. Portuguese.

4

The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.

Malaquias AC, Scalco RC, Fontenele EG, Costalonga EF, Baldin AD, Braz AF, Funari MF, Nishi MY, Guerra-Junior G, Mendonca BB, Arnhold IJ, Jorge AA. Malaquias AC, et al. Horm Res Paediatr. 2013;80(6):449-56. doi: 10.1159/000355411. Epub 2013 Nov 26. Horm Res Paediatr. 2013. PMID: 24296787

5

Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism.

Braz AF, Costalonga EF, Trarbach EB, Scalco RC, Malaquias AC, Guerra-Junior G, Antonini SR, Mendonca BB, Arnhold IJ, Jorge AA. Braz AF, et al. Among authors: scalco rc. J Clin Endocrinol Metab. 2014 Sep;99(9):E1808-13. doi: 10.1210/jc.2014-1744. Epub 2014 Jun 6. J Clin Endocrinol Metab. 2014. PMID: 24905066

6

STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability.

Scalco RC, Hwa V, Domené HM, Jasper HG, Belgorosky A, Marino R, Pereira AM, Tonelli CA, Wit JM, Rosenfeld RG, Jorge AA. Scalco RC, et al. Eur J Endocrinol. 2015 Sep;173(3):291-6. doi: 10.1530/EJE-15-0398. Epub 2015 Jun 1. Eur J Endocrinol. 2015. PMID: 26034074 Free PMC article.

7

MANAGEMENT OF ENDOCRINE DISEASE: Diagnostic and therapeutic approach of tall stature.

Albuquerque EVA, Scalco RC, Jorge AAL. Albuquerque EVA, et al. Eur J Endocrinol. 2017 Jun;176(6):R339-R353. doi: 10.1530/EJE-16-1054. Epub 2017 Mar 8. Eur J Endocrinol. 2017. PMID: 28274950 Review.

8

Growth hormone insensitivity with immune dysfunction caused by a STAT5B mutation in the south of Brazil: evidence for a founder effect.

Scalco RC, Gonçalves FT, Santos HC, Cardena MMSG, Tonelli CA, Funari MFA, Aracava RM, Pereira AC, Fridman C, Jorge AAL. Scalco RC, et al. Genet Mol Biol. 2017 Apr-Jun;40(2):436-441. doi: 10.1590/1678-4685-GMB-2016-0231. Epub 2017 Jun 5. Genet Mol Biol. 2017. PMID: 28590503 Free PMC article.

9

IGF-1 assessed by pubertal status has the best positive predictive power for GH deficiency diagnosis in peripubertal children.

Inoue-Lima TH, Vasques GA, Scalco RC, Nakaguma M, Mendonca BB, Arnhold IJP, Jorge AAL. Inoue-Lima TH, et al. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):173-179. doi: 10.1515/jpem-2018-0435. J Pediatr Endocrinol Metab. 2019. PMID: 30676998

10

Impact of Long-Term Dexamethasone Therapy on the Metabolic Profile of Patients With 21-Hydroxylase Deficiency.

Seraphim CE, Frassei JS, Pessoa BS, Scalco RC, Miranda MC, Madureira G, Mendonca BB, Bachega TASS. Seraphim CE, et al. J Endocr Soc. 2019 Jun 19;3(8):1574-1582. doi: 10.1210/js.2019-00123. eCollection 2019 Aug 1. J Endocr Soc. 2019. PMID: 31384718 Free PMC article.

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