Costa EM - Search Results

1

Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer.

Bianchi PH, Gouveia GR, Costa EM, Domenice S, Martin RM, de Carvalho LC, Pelaes T, Inacio M, Codarin RR, Sator de Faria MB, Francisco RP, Baracat EC, Serafini PC, Mendonca BB. Bianchi PH, et al. Among authors: costa em. J Clin Endocrinol Metab. 2016 Feb;101(2):345-8. doi: 10.1210/jc.2015-3201. Epub 2015 Dec 8. J Clin Endocrinol Metab. 2016. PMID: 26647153

2

Androgen insensitivity syndrome: a review.

Batista RL, Costa EMF, Rodrigues AS, Gomes NL, Faria JA Jr, Nishi MY, Arnhold IJP, Domenice S, Mendonca BB. Batista RL, et al. Arch Endocrinol Metab. 2018 Mar-Apr;62(2):227-235. doi: 10.20945/2359-3997000000031. Arch Endocrinol Metab. 2018. PMID: 29768628 Free PMC article. Review.

3

Impact of schooling in the HIV/AIDS prevalence among Brazilian transgender women.

Batista RL, Verduguez EDR, Inacio M, Cunha FS, Marques MD, Gomes NLRA, Faria JAD Jr, Sircili MHP, Mendonça BB, Costa EMF, Domenice S. Batista RL, et al. Arch Endocrinol Metab. 2020 Aug;64(4):369-373. doi: 10.20945/2359-3997000000260. Epub 2020 Jun 5. Arch Endocrinol Metab. 2020. PMID: 32813764 Free PMC article.

4

Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction.

Costa EM, Bedecarrats GY, Mendonca BB, Arnhold IJ, Kaiser UB, Latronico AC. Costa EM, et al. J Clin Endocrinol Metab. 2001 Jun;86(6):2680-6. doi: 10.1210/jcem.86.6.7551. J Clin Endocrinol Metab. 2001. PMID: 11397871

5

Management of ambiguous genitalia in pseudohermaphrodites: new perspectives on vaginal dilation.

Costa EM, Mendonca BB, Inácio M, Arnhold IJ, Silva FA, Lodovici O. Costa EM, et al. Fertil Steril. 1997 Feb;67(2):229-32. doi: 10.1016/s0015-0282(97)81902-4. Fertil Steril. 1997. PMID: 9022594 Free article.

6

Male pseudohermaphroditism due to steroid 5alpha-reductase 2 deficiency. Diagnosis, psychological evaluation, and management.

Mendonca BB, Inacio M, Costa EM, Arnhold IJ, Silva FA, Nicolau W, Bloise W, Russel DW, Wilson JD. Mendonca BB, et al. Among authors: costa em. Medicine (Baltimore). 1996 Mar;75(2):64-76. doi: 10.1097/00005792-199603000-00003. Medicine (Baltimore). 1996. PMID: 8606628 Free article.

7

Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency. Diagnosis, psychological evaluation, and management.

Mendonca BB, Inacio M, Arnhold IJ, Costa EM, Bloise W, Martin RM, Denes FT, Silva FA, Andersson S, Lindqvist A, Wilson JD. Mendonca BB, et al. Among authors: costa em. Medicine (Baltimore). 2000 Sep;79(5):299-309. doi: 10.1097/00005792-200009000-00003. Medicine (Baltimore). 2000. PMID: 11039078 Free article.

8

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism.

Teles MG, Trarbach EB, Noel SD, Guerra-Junior G, Jorge A, Beneduzzi D, Bianco SD, Mukherjee A, Baptista MT, Costa EM, De Castro M, Mendonça BB, Kaiser UB, Latronico AC. Teles MG, et al. Among authors: costa em. Eur J Endocrinol. 2010 Jul;163(1):29-34. doi: 10.1530/EJE-10-0012. Epub 2010 Apr 6. Eur J Endocrinol. 2010. PMID: 20371656

9

A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.

Melo KF, Latronico AC, Costa EM, Billerbeck AE, Mendonca BB, Arnhold IJ. Melo KF, et al. Among authors: costa em. Hum Mutat. 1999 Oct;14(4):353. doi: 10.1002/(SICI)1098-1004(199910)14:4<353::AID-HUMU16>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10502786

10

The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

Oliveira LM, Seminara SB, Beranova M, Hayes FJ, Valkenburgh SB, Schipani E, Costa EM, Latronico AC, Crowley WF Jr, Vallejo M. Oliveira LM, et al. Among authors: costa em. J Clin Endocrinol Metab. 2001 Apr;86(4):1532-8. doi: 10.1210/jcem.86.4.7420. J Clin Endocrinol Metab. 2001. PMID: 11297579

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