Mendonca BB - Search Results

1

Clinical, hormonal, ovarian, and genetic aspects of 46,XX patients with congenital adrenal hyperplasia due to CYP17A1 defects.

Carvalho LC, Brito VN, Martin RM, Zamboni AM, Gomes LG, Inácio M, Mermejo LM, Coeli-Lacchini F, Teixeira VR, Gonçalves FT, Carrilho AJ, Del Toro Camargo KY, Finkielstain GP, Taboada GF, Frade Costa EM, Domenice S, Mendonca BB. Carvalho LC, et al. Among authors: mendonca bb. Fertil Steril. 2016 Jun;105(6):1612-9. doi: 10.1016/j.fertnstert.2016.02.008. Epub 2016 Feb 23. Fertil Steril. 2016. PMID: 26920256 Free article.

2

Detection of Y-specific sequences in 122 patients with Turner syndrome: nested PCR is not a reliable method.

Nishi MY, Domenice S, Medeiros MA, Mendonca BB, Billerbeck AE. Nishi MY, et al. Among authors: mendonca bb. Am J Med Genet. 2002 Feb 1;107(4):299-305. doi: 10.1002/ajmg.10168. Am J Med Genet. 2002. PMID: 11840486 Clinical Trial.

3

An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.

Melo KF, Martin RM, Costa EM, Carvalho FM, Jorge AA, Arnhold IJ, Mendonca BB. Melo KF, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Jun;87(6):2500-5. doi: 10.1210/jcem.87.6.8521. J Clin Endocrinol Metab. 2002. PMID: 12050205 Review.

4

Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene.

Fragoso MC, Domenice S, Latronico AC, Martin RM, Pereira MA, Zerbini MC, Lucon AM, Mendonca BB. Fragoso MC, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2003 May;88(5):2147-51. doi: 10.1210/jc.2002-021362. J Clin Endocrinol Metab. 2003. PMID: 12727968

5

Familial hyperestrogenism in both sexes: clinical, hormonal, and molecular studies of two siblings.

Martin RM, Lin CJ, Nishi MY, Billerbeck AE, Latronico AC, Russell DW, Mendonca BB. Martin RM, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2003 Jul;88(7):3027-34. doi: 10.1210/jc.2002-021780. J Clin Endocrinol Metab. 2003. PMID: 12843139

6

Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene.

Melo KF, Mendonca BB, Billerbeck AE, Costa EM, Inácio M, Silva FA, Leal AM, Latronico AC, Arnhold IJ. Melo KF, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2003 Jul;88(7):3241-50. doi: 10.1210/jc.2002-021658. J Clin Endocrinol Metab. 2003. PMID: 12843171

7

P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.

Martin RM, Lin CJ, Costa EM, de Oliveira ML, Carrilho A, Villar H, Longui CA, Mendonca BB. Martin RM, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2003 Dec;88(12):5739-46. doi: 10.1210/jc.2003-030988. J Clin Endocrinol Metab. 2003. PMID: 14671162

8

A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency.

Correa RV, Domenice S, Bingham NC, Billerbeck AE, Rainey WE, Parker KL, Mendonca BB. Correa RV, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2004 Apr;89(4):1767-72. doi: 10.1210/jc.2003-031240. J Clin Endocrinol Metab. 2004. PMID: 15070943

9

Assessment of the role of transcript for GATA-4 as a marker of unfavorable outcome in human adrenocortical neoplasms.

Barbosa AS, Giacaglia LR, Martin RM, Mendonca BB, Lin CJ. Barbosa AS, et al. Among authors: mendonca bb. BMC Endocr Disord. 2004 Jul 7;4(1):3. doi: 10.1186/1472-6823-4-3. BMC Endocr Disord. 2004. PMID: 15239841 Free PMC article.

10

A single luteinizing hormone determination 2 hours after depot leuprolide is useful for therapy monitoring of gonadotropin-dependent precocious puberty in girls.

Brito VN, Latronico AC, Arnhold IJ, Mendonca BB. Brito VN, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2004 Sep;89(9):4338-42. doi: 10.1210/jc.2003-031537. J Clin Endocrinol Metab. 2004. PMID: 15356030

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