Brito VN - Search Results

1

Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study.

Canton APM, Tinano FR, Guasti L, Montenegro LR, Ryan F, Shears D, de Melo ME, Gomes LG, Piana MP, Brauner R, Espino-Aguilar R, Escribano-Muñoz A, Paganoni A, Read JE, Korbonits M, Seraphim CE, Costa SS, Krepischi AC, Jorge AAL, David A, Kaisinger LR, Ong KK, Perry JRB, Abreu AP, Kaiser UB, Argente J, Mendonca BB, Brito VN, Howard SR, Latronico AC. Canton APM, et al. Among authors: brito vn. Lancet Diabetes Endocrinol. 2023 Aug;11(8):545-554. doi: 10.1016/S2213-8587(23)00131-6. Epub 2023 Jun 26. Lancet Diabetes Endocrinol. 2023. PMID: 37385287 Free PMC article.

2

A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty.

Latronico AC, Abell AN, Arnhold IJ, Liu X, Lins TS, Brito VN, Billerbeck AE, Segaloff DL, Mendonca BB. Latronico AC, et al. Among authors: brito vn. J Clin Endocrinol Metab. 1998 Jul;83(7):2435-40. doi: 10.1210/jcem.83.7.4968. J Clin Endocrinol Metab. 1998. PMID: 9661624

3

Diagnostic value of fluorometric assays in the evaluation of precocious puberty.

Brito VN, Batista MC, Borges MF, Latronico AC, Kohek MB, Thirone AC, Jorge BH, Arnhold IJ, Mendonca BB. Brito VN, et al. J Clin Endocrinol Metab. 1999 Oct;84(10):3539-44. doi: 10.1210/jcem.84.10.6024. J Clin Endocrinol Metab. 1999. PMID: 10522992

4

The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes.

Latronico AC, Lins TS, Brito VN, Arnhold IJ, Mendonca BB. Latronico AC, et al. Among authors: brito vn. Clin Endocrinol (Oxf). 2000 Nov;53(5):609-13. doi: 10.1046/j.1365-2265.2000.01135.x. Clin Endocrinol (Oxf). 2000. PMID: 11106922

5

Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene.

Domenice S, Latronico AC, Brito VN, Arnhold IJ, Kok F, Mendonca BB. Domenice S, et al. Among authors: brito vn. J Clin Endocrinol Metab. 2001 Sep;86(9):4068-71. doi: 10.1210/jcem.86.9.7816. J Clin Endocrinol Metab. 2001. PMID: 11549627

6

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. J Clin Endocrinol Metab. 2004 Sep;89(9):4338-42. doi: 10.1210/jc.2003-031537. J Clin Endocrinol Metab. 2004. PMID: 15356030

7

Clinical and hormonal features of selective follicle-stimulating hormone (FSH) deficiency due to FSH beta-subunit gene mutations in both sexes.

Berger K, Souza H, Brito VN, d'Alva CB, Mendonca BB, Latronico AC. Berger K, et al. Among authors: brito vn. Fertil Steril. 2005 Feb;83(2):466-70. doi: 10.1016/j.fertnstert.2004.06.069. Fertil Steril. 2005. PMID: 15705395 Free article.

8

Allelic variants of the gamma-aminobutyric acid-A receptor alpha1-subunit gene (GABRA1) are not associated with idiopathic gonadotropin-dependent precocious puberty in girls with and without electroencephalographic abnormalities.

Brito VN, Mendonca BB, Guilhoto LM, Freitas KC, Arnhold IJ, Latronico AC. Brito VN, et al. J Clin Endocrinol Metab. 2006 Jun;91(6):2432-6. doi: 10.1210/jc.2005-2657. Epub 2006 Mar 28. J Clin Endocrinol Metab. 2006. PMID: 16569738

9

Preclinical diagnosis of testotoxicosis in a boy with an activating mutation of the luteinizing hormone receptor.

Teles M, Brito VN, Arnhold IJ, Mendonca BB, Latronico AC. Teles M, et al. Among authors: brito vn. J Pediatr Endocrinol Metab. 2006 Apr;19(4):541-4. J Pediatr Endocrinol Metab. 2006. PMID: 16759041

10

A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty.

d'Alva CB, Brito VN, Palhares HM, Carvalho FM, Arnhold IJ, Mendonca BB, Latronico AC. d'Alva CB, et al. Among authors: brito vn. Clin Endocrinol (Oxf). 2006 Sep;65(3):408-10. doi: 10.1111/j.1365-2265.2006.02596.x. Clin Endocrinol (Oxf). 2006. PMID: 16918965 No abstract available.

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