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The phenotypic spectrum associated with OTX2 mutations in humans.
Gregory LC, Gergics P, Nakaguma M, Bando H, Patti G, McCabe MJ, Fang Q, Ma Q, Ozel AB, Li JZ, Poina MM, Jorge AAL, Benedetti AFF, Lerario AM, Arnhold IJP, Mendonca BB, Maghnie M, Camper SA, Carvalho LRS, Dattani MT. Gregory LC, et al. Among authors: lerario am. Eur J Endocrinol. 2021 May 25;185(1):121-135. doi: 10.1530/EJE-20-1453. Eur J Endocrinol. 2021. PMID: 33950863 Free PMC article.
[Molecular mechanisms involved in adrenocortical tumorigenesis].
Lerario AM, Mendonça BB, Lin CJ. Lerario AM, et al. Arq Bras Endocrinol Metabol. 2005 Oct;49(5):753-68. doi: 10.1590/s0004-27302005000500016. Epub 2006 Jan 23. Arq Bras Endocrinol Metabol. 2005. PMID: 16444358 Review. Portuguese.
Steroidogenic factor 1 overexpression and gene amplification are more frequent in adrenocortical tumors from children than from adults.
Almeida MQ, Soares IC, Ribeiro TC, Fragoso MC, Marins LV, Wakamatsu A, Ressio RA, Nishi MY, Jorge AA, Lerario AM, Alves VA, Mendonca BB, Latronico AC. Almeida MQ, et al. Among authors: lerario am. J Clin Endocrinol Metab. 2010 Mar;95(3):1458-62. doi: 10.1210/jc.2009-2040. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080844
Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor.
Lima Lde O, Lerario AM, Alencar GA, Brito LP, Almeida MQ, Domenice S, Latronico AC, Mendonca BB, Fragoso MC. Lima Lde O, et al. Among authors: lerario am. Arq Bras Endocrinol Metabol. 2011 Feb;55(1):72-7. doi: 10.1590/s0004-27302011000100010. Arq Bras Endocrinol Metabol. 2011. PMID: 21468523
Combined expression of BUB1B, DLGAP5, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients.
Fragoso MC, Almeida MQ, Mazzuco TL, Mariani BM, Brito LP, Gonçalves TC, Alencar GA, Lima Lde O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Fragoso MC, et al. Among authors: lerario am. Eur J Endocrinol. 2012 Jan;166(1):61-7. doi: 10.1530/EJE-11-0806. Epub 2011 Nov 2. Eur J Endocrinol. 2012. PMID: 22048964
ARMC5 mutations are a frequent cause of primary macronodular adrenal Hyperplasia.
Alencar GA, Lerario AM, Nishi MY, Mariani BM, Almeida MQ, Tremblay J, Hamet P, Bourdeau I, Zerbini MC, Pereira MA, Gomes GC, Rocha Mde S, Chambo JL, Lacroix A, Mendonca BB, Fragoso MC. Alencar GA, et al. Among authors: lerario am. J Clin Endocrinol Metab. 2014 Aug;99(8):E1501-9. doi: 10.1210/jc.2013-4237. Epub 2014 Apr 7. J Clin Endocrinol Metab. 2014. PMID: 24708098
128 results