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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 1
2011 1
2013 1
2014 2
2016 1
2019 2
2020 4
2021 3
2022 1
2024 0

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14 results

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Page 1
Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.
Domenice S, Machado AZ, Ferreira FM, Ferraz-de-Souza B, Lerario AM, Lin L, Nishi MY, Gomes NL, da Silva TE, Silva RB, Correa RV, Montenegro LR, Narciso A, Costa EM, Achermann JC, Mendonca BB. Domenice S, et al. Among authors: montenegro lr. Birth Defects Res C Embryo Today. 2016 Dec;108(4):309-320. doi: 10.1002/bdrc.21145. Birth Defects Res C Embryo Today. 2016. PMID: 28033660 Free PMC article. Review.
Role of the Mevalonate Pathway in Adrenocortical Tumorigenesis.
Lima-Valassi HP, Lerario AM, Montenegro LR, Fragoso MCBV, Almeida MQ, Mendonca BB, Lin CJ. Lima-Valassi HP, et al. Among authors: montenegro lr. Horm Metab Res. 2021 Feb;53(2):124-131. doi: 10.1055/a-1322-2943. Epub 2020 Dec 11. Horm Metab Res. 2021. PMID: 33307558
Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development.
Gomes NL, Batista RL, Nishi MY, Lerário AM, Silva TE, de Moraes Narcizo A, Benedetti AFF, de Assis Funari MF, Faria Junior JA, Moraes DR, Quintão LML, Montenegro LR, Ferrari MTM, Jorge AA, Arnhold IJP, Costa EMF, Domenice S, Mendonca BB. Gomes NL, et al. Among authors: montenegro lr. J Clin Endocrinol Metab. 2022 Apr 19;107(5):e1797-e1806. doi: 10.1210/clinem/dgac064. J Clin Endocrinol Metab. 2022. PMID: 35134971
Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum.
Nakaguma M, Ferreira NGBP, Benedetti AFF, Madi MC, Silva JM, Li JZ, Ma Q, Bilge Ozel A, Fang Q, Narcizo AM, Cardoso LC, Montenegro LR, Funari MFA, Nishi MY, Arnhold IJP, Jorge AAL, Mendonca BB, Camper SA, Carvalho LR. Nakaguma M, et al. Among authors: montenegro lr. Genes (Basel). 2021 Jul 25;12(8):1128. doi: 10.3390/genes12081128. Genes (Basel). 2021. PMID: 34440302 Free PMC article.
New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism.
Amato LGL, Montenegro LR, Lerario AM, Jorge AAL, Guerra Junior G, Schnoll C, Renck AC, Trarbach EB, Costa EMF, Mendonca BB, Latronico AC, Silveira LFG. Amato LGL, et al. Among authors: montenegro lr. Eur J Endocrinol. 2019 Aug 1;181(2):103-119. doi: 10.1530/EJE-18-0764. Eur J Endocrinol. 2019. PMID: 31200363
Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier ML, Santana L, Honjo RS, Kim CA, de Zegher F, Idkowiak J, Gilligan LC, Arlt W, Funari MFA, Jorge AAL, Mendonca BB, Netchine I, Brito VN, Latronico AC. Canton APM, et al. Among authors: montenegro lr. Hum Reprod. 2021 Jan 25;36(2):506-518. doi: 10.1093/humrep/deaa306. Hum Reprod. 2021. PMID: 33313884
SELAdb: A database of exonic variants in a Brazilian population referred to a quaternary medical center in São Paulo.
Lerario AM, Mohan DR, Montenegro LR, Funari MFA, Nishi MY, Narcizo AM, Benedetti AFF, Oba-Shinjo SM, Vitorino AJ, Santos RASXD, Jorge AAL, Onuchic LF, Marie SKN, Mendonca BB. Lerario AM, et al. Among authors: montenegro lr. Clinics (Sao Paulo). 2020;75:e1913. doi: 10.6061/clinics/2020/e1913. Epub 2020 Aug 10. Clinics (Sao Paulo). 2020. PMID: 32785571 Free PMC article.
14 results