Latronico AC - Search Results

1

Mutational analysis of the genes encoding RFamide-related peptide-3, the human orthologue of gonadotrophin-inhibitory hormone, and its receptor (GPR147) in patients with gonadotrophin-releasing hormone-dependent pubertal disorders.

Lima CJ, Cardoso SC, Lemos EF, Zingler E, Capanema C, Menezes LD, Vogado G, Dos Santos BT, de Moraes OL, Duarte EF, de Brito VN, Latronico AC, Lofrano-Porto A. Lima CJ, et al. Among authors: latronico ac. J Neuroendocrinol. 2014 Nov;26(11):817-24. doi: 10.1111/jne.12207. J Neuroendocrinol. 2014. PMID: 25180599

2

Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depot.

de Brito VN, Latronico AC, Arnhold IJ, Lo LS, Domenice S, Albano MC, Fragoso MC, Mendonca BB. de Brito VN, et al. Among authors: latronico ac. Arch Dis Child. 1999 Mar;80(3):231-4. doi: 10.1136/adc.80.3.231. Arch Dis Child. 1999. PMID: 10325702 Free PMC article.

3

Luteinizing hormone beta mutation and hypogonadism in men and women.

Lofrano-Porto A, Barra GB, Giacomini LA, Nascimento PP, Latronico AC, Casulari LA, da Rocha Neves Fde A. Lofrano-Porto A, et al. Among authors: latronico ac. N Engl J Med. 2007 Aug 30;357(9):897-904. doi: 10.1056/NEJMoa071999. N Engl J Med. 2007. PMID: 17761593 Free article.

4

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.

Abreu AP, Trarbach EB, de Castro M, Frade Costa EM, Versiani B, Matias Baptista MT, Garmes HM, Mendonca BB, Latronico AC. Abreu AP, et al. Among authors: latronico ac. J Clin Endocrinol Metab. 2008 Oct;93(10):4113-8. doi: 10.1210/jc.2008-0958. Epub 2008 Aug 5. J Clin Endocrinol Metab. 2008. PMID: 18682503

5

Inactivating mutations of luteinizing hormone beta-subunit or luteinizing hormone receptor cause oligo-amenorrhea and infertility in women.

Arnhold IJ, Lofrano-Porto A, Latronico AC. Arnhold IJ, et al. Among authors: latronico ac. Horm Res. 2009;71(2):75-82. doi: 10.1159/000183895. Epub 2009 Jan 8. Horm Res. 2009. PMID: 19129711 Review.

6

Genetics basis for GnRH-dependent pubertal disorders in humans.

Silveira LF, Trarbach EB, Latronico AC. Silveira LF, et al. Among authors: latronico ac. Mol Cell Endocrinol. 2010 Aug 5;324(1-2):30-8. doi: 10.1016/j.mce.2010.02.023. Epub 2010 Feb 25. Mol Cell Endocrinol. 2010. PMID: 20188792 Review.

7

The role of prokineticins in the pathogenesis of hypogonadotropic hypogonadism.

Abreu AP, Kaiser UB, Latronico AC. Abreu AP, et al. Among authors: latronico ac. Neuroendocrinology. 2010;91(4):283-90. doi: 10.1159/000308880. Epub 2010 May 21. Neuroendocrinology. 2010. PMID: 20502053 Free PMC article. Review.

8

New genetic factors implicated in human GnRH-dependent precocious puberty: the role of kisspeptin system.

Teles MG, Silveira LF, Tusset C, Latronico AC. Teles MG, et al. Among authors: latronico ac. Mol Cell Endocrinol. 2011 Oct 22;346(1-2):84-90. doi: 10.1016/j.mce.2011.05.019. Epub 2011 Jun 1. Mol Cell Endocrinol. 2011. PMID: 21664234 Review.

9

Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism.

Beneduzzi D, Trarbach EB, Latronico AC, Mendonca BB, Silveira LF. Beneduzzi D, et al. Among authors: latronico ac. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):540-4. doi: 10.1590/s0004-27302012000800013. Arq Bras Endocrinol Metabol. 2012. PMID: 23295295

10

Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders.

Tusset C, Noel SD, Trarbach EB, Silveira LF, Jorge AA, Brito VN, Cukier P, Seminara SB, Mendonça BB, Kaiser UB, Latronico AC. Tusset C, et al. Among authors: latronico ac. Arq Bras Endocrinol Metabol. 2012 Dec;56(9):646-52. doi: 10.1590/s0004-27302012000900008. Arq Bras Endocrinol Metabol. 2012. PMID: 23329188 Free PMC article.

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