Mendonca B - Search Results

1

Retrospective Analysis of Prognostic Factors in Pediatric Patients with Adrenocortical Tumor from Unique Tertiary Center with Long-Term Follow-Up.

Bachega FS, Suartz CV, Almeida MQ, Brondani VB, Charchar HLS, Lacombe AMF, Martins-Filho SN, Soares IC, Zerbini MCN, Dénes FT, Mendonca B, Lopes RI, Latronico AC, Fragoso MCBV. Bachega FS, et al. Among authors: mendonca b. J Clin Med. 2022 Nov 9;11(22):6641. doi: 10.3390/jcm11226641. J Clin Med. 2022. PMID: 36431124 Free PMC article. Review.

2

No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumors.

Giacaglia LR, Kohek MB da F, Carvalho FM, Fragoso MC, Mendonca B, Latronico AC. Giacaglia LR, et al. Among authors: mendonca b. Fertil Steril. 2000 Nov;74(5):992-5. doi: 10.1016/s0015-0282(00)01565-x. Fertil Steril. 2000. PMID: 11056247 Free article.

3

Detection of gsp somatic mutation through direct sequencing of heteroduplex alleles disclosed by denaturing gradient gel electrophoresis.

Fragoso MC, Lando VS, Latronico AC, Frazzatto ET, Russell AJ, Mendonca BB. Fragoso MC, et al. Among authors: mendonca bb. Med Sci Monit. 2002 Jan;8(1):BR15-8. Med Sci Monit. 2002. PMID: 11782667

4

Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene.

Mendonca BB, Leite MV, de Castro M, Kino T, Elias LL, Bachega TA, Arnhold IJ, Chrousos GP, Latronico AC. Mendonca BB, et al. J Clin Endocrinol Metab. 2002 Apr;87(4):1805-9. doi: 10.1210/jcem.87.4.8379. J Clin Endocrinol Metab. 2002. PMID: 11932321

5

Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.

Osorio MG, Marui S, Jorge AA, Latronico AC, Lo LS, Leite CC, Estefan V, Mendonca BB, Arnhold IJ. Osorio MG, et al. Among authors: mendonca bb. J Clin Endocrinol Metab. 2002 Nov;87(11):5076-84. doi: 10.1210/jc.2001-011936. J Clin Endocrinol Metab. 2002. PMID: 12414875

6

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. J Clin Endocrinol Metab. 2003 May;88(5):2147-51. doi: 10.1210/jc.2002-021362. J Clin Endocrinol Metab. 2003. PMID: 12727968

7

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

8

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

9

Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty.

Latronico AC, Billerbeck AE, Pinto EM, Brazil D'Alva C, Arnhold IJ, Mendonca BB. Latronico AC, et al. Among authors: mendonca bb. Clin Endocrinol (Oxf). 2003 Oct;59(4):533-4. doi: 10.1046/j.1365-2265.2003.01810.x. Clin Endocrinol (Oxf). 2003. PMID: 14510919 No abstract available.

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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