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Filtros : "Financiamento FAPESP" "Espanha" "Argente, Jesús" Limpar

Filtros

USP affiliated authors
- brito, vinicius nahime de (2)
- mendonça, berenice bilharinho de (2)
- montenegro, luciana ribeiro (2)
- antonini, sonir roberto rauber (1)
- canton, ana pinheiro machado (1)

Indexado em
- indexado no current contents (1)
- indexado no embase (1)
- indexado no global health (1)
- indexado no medline (1)
- indexado no pubmed (1)

Collaboration
Normalized affiliation
Non normalized affiliation
- centro de investigaciones endocrinológicas "dr. césar bergadá" (consejo nacional de investigaciones científicas y técnicas - fei - división de endocrinología, hospital de niños ricardo gutiérrez), buenos aires (1)
- departamento de saúde integrada da universidade do estado do pará (uepa), santarém, pará (1)
- department of pediatrics, iis-fundación jiménez díaz, universidad autónoma de madrid, spanish pubere registry, madrid (1)
- division of endocrinology, diabetes and hypertension, department of medicine, brigham and women's hospital, harvard medical school, boston, ma (1)
- division of endocrinology, diabetes, and metabolism, nemours children's clinic, jacksonville, fl (1)

Artigo de periodico
Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series (2025)
Faria, Aline Guimarães; Montenegro, Luciana Ribeiro ; Jorge, Alexander Augusto de Lima ; Martin, Regina Matsunaga ; Fragoso, Maria Candida Barisson Villares ; Tinano, Flavia Rezende ; Seraphim, Carlos Eduardo ; Canton, Ana Pinheiro Machado ; Gomes, Larissa Garcia ; Moreno, Gabriel A. Martos ; García, Irene Tarjuelo; Carcavilla, Atilano ; Capistros, Mireia Tirado ; Souza-Pinto, Nadja Cristhina de ; Argente, Jesús ; Latronico, Ana Claudia ; Mendonca, Berenice Bilharinho de ; Brito, Vinicius Nahime de
Source: Archives of Endocrinology and Metabolism. Unidades: FM, IQ
Subjects: PUBERDADE PRECOCE, LEUCÓCITOS, REAÇÃO EM CADEIA POR POLIMERASE, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FARIA, Aline Guimarães et al. Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series. Archives of Endocrinology and Metabolism, v. 69, n. 2, p. 1-10 art. e240459, 2025Tradução . . Disponível em: https://dx.doi.org/10.20945/2359-4292-2024-0459. Acesso em: 08 out. 2025.
APA
Faria, A. G., Montenegro, L. R., Jorge, A. A. de L., Martin, R. M., Fragoso, M. C. B. V., Tinano, F. R., et al. (2025). Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series. Archives of Endocrinology and Metabolism, 69( 2), 1-10 art. e240459. doi:10.20945/2359-4292-2024-0459
NLM
Faria AG, Montenegro LR, Jorge AA de L, Martin RM, Fragoso MCBV, Tinano FR, Seraphim CE, Canton APM, Gomes LG, Moreno GAM, García IT, Carcavilla A, Capistros MT, Souza-Pinto NC de, Argente J, Latronico AC, Mendonca BB de, Brito VN de. Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series [Internet]. Archives of Endocrinology and Metabolism. 2025 ; 69( 2): 1-10 art. e240459.[citado 2025 out. 08 ] Available from: https://dx.doi.org/10.20945/2359-4292-2024-0459
Vancouver
Faria AG, Montenegro LR, Jorge AA de L, Martin RM, Fragoso MCBV, Tinano FR, Seraphim CE, Canton APM, Gomes LG, Moreno GAM, García IT, Carcavilla A, Capistros MT, Souza-Pinto NC de, Argente J, Latronico AC, Mendonca BB de, Brito VN de. Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series [Internet]. Archives of Endocrinology and Metabolism. 2025 ; 69( 2): 1-10 art. e240459.[citado 2025 out. 08 ] Available from: https://dx.doi.org/10.20945/2359-4292-2024-0459
Artigo de periodico
Genotype–phenotype correlations in central precocious puberty caused by MKRN3 mutations (2021)
Seraphim, Carlos Eduardo ; Canton, Ana Pinheiro Machado ; Montenegro, Luciana Ribeiro; Piovesan, Maiara Ribeiro ; Macedo, Delanie B.; Cunha, Marina; Guimaraes, Aline; Ramos, Carolina Oliveira; Benedetti, Anna Flavia Figueredo; Leal, Andréa de Castro; Gagliardi, Priscila C.; Antonini, Sonir Roberto Rauber ; Gryngarten, Mirta; Arcari, Andrea J.; Abreu, Ana Paula; Kaiser, Ursula B.; Soriano-Guillen, Leandro; Escribano-Muñoz, Arancha; Corripio, Raquel; Labarta, José I; Travieso-Suárez, Lourdes; Ortiz-Cabrera, Nelmar Valentina; Argente, Jesús; Mendonca, Berenice Bilharinho de ; Brito, Vinicius Nahime de ; Latronico, Ana Claudia
Source: Journal of Clinical Endocrinology and Metabolism. Unidades: FMRP, FM
Subjects: GENÓTIPOS, FENÓTIPOS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERAPHIM, Carlos Eduardo et al. Genotype–phenotype correlations in central precocious puberty caused by MKRN3 mutations. Journal of Clinical Endocrinology and Metabolism, v. 106, n. 4, p. 1041-1050, 2021Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgaa955. Acesso em: 08 out. 2025.
APA
Seraphim, C. E., Canton, A. P. M., Montenegro, L. R., Piovesan, M. R., Macedo, D. B., Cunha, M., et al. (2021). Genotype–phenotype correlations in central precocious puberty caused by MKRN3 mutations. Journal of Clinical Endocrinology and Metabolism, 106( 4), 1041-1050. doi:10.1210/clinem/dgaa955
NLM
Seraphim CE, Canton APM, Montenegro LR, Piovesan MR, Macedo DB, Cunha M, Guimaraes A, Ramos CO, Benedetti AFF, Leal A de C, Gagliardi PC, Antonini SRR, Gryngarten M, Arcari AJ, Abreu AP, Kaiser UB, Soriano-Guillen L, Escribano-Muñoz A, Corripio R, Labarta JI, Travieso-Suárez L, Ortiz-Cabrera NV, Argente J, Mendonca BB de, Brito VN de, Latronico AC. Genotype–phenotype correlations in central precocious puberty caused by MKRN3 mutations [Internet]. Journal of Clinical Endocrinology and Metabolism. 2021 ; 106( 4): 1041-1050.[citado 2025 out. 08 ] Available from: https://doi.org/10.1210/clinem/dgaa955
Vancouver
Seraphim CE, Canton APM, Montenegro LR, Piovesan MR, Macedo DB, Cunha M, Guimaraes A, Ramos CO, Benedetti AFF, Leal A de C, Gagliardi PC, Antonini SRR, Gryngarten M, Arcari AJ, Abreu AP, Kaiser UB, Soriano-Guillen L, Escribano-Muñoz A, Corripio R, Labarta JI, Travieso-Suárez L, Ortiz-Cabrera NV, Argente J, Mendonca BB de, Brito VN de, Latronico AC. Genotype–phenotype correlations in central precocious puberty caused by MKRN3 mutations [Internet]. Journal of Clinical Endocrinology and Metabolism. 2021 ; 106( 4): 1041-1050.[citado 2025 out. 08 ] Available from: https://doi.org/10.1210/clinem/dgaa955

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