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Filtros : "Financiamento FAPESP" "Indexado no SCOPUS" "Financiamento NICHD" Limpar

Filtros

USP affiliated authors
- antonini, sonir roberto rauber (2)
- brito, vinicius nahime de (1)
- mendonça, berenice bilharinho de (1)
- montenegro, luciana ribeiro (1)
- piovesan, maiara ribeiro (1)

Indexado em
- indexado no current contents (2)
- indexado no embase (2)
- indexado no global health (2)
- indexado no medline (2)
- indexado no pubmed (2)

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 endocrinology, institute of zoology, jagiellonian university in krakow, gronostajowa, krakow (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)

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
Artigo de periodico
Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation (2021)
Leal, Leticia Ferro; Szarek, Eva; Berthon, Annabel; Nesterova, Maria; Faucz, Fabio R; London, Edra; Mercier, Christopher; Abu-Asab, Mones; Starost, Matthew F; Dye, Louis; Bilinska, Barbara; Kotula-Balak, Malgorzata; Antonini, Sonir Roberto Rauber ; Stratakis, Constantine A
Source: Molecular and Cellular Endocrinology. Unidade: FMRP
Subjects: TRANSDUÇÃO DE SINAL CELULAR, GLÂNDULAS SUPRARRENAIS, ALDOSTERONA, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, CRUZAMENTOS, PROTEÍNAS QUINASES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEAL, Leticia Ferro et al. Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation. Molecular and Cellular Endocrinology, v. 15, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2020.111117. Acesso em: 08 out. 2025.
APA
Leal, L. F., Szarek, E., Berthon, A., Nesterova, M., Faucz, F. R., London, E., et al. (2021). Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation. Molecular and Cellular Endocrinology, 15. doi:10.1016/j.mce.2020.111117
NLM
Leal LF, Szarek E, Berthon A, Nesterova M, Faucz FR, London E, Mercier C, Abu-Asab M, Starost MF, Dye L, Bilinska B, Kotula-Balak M, Antonini SRR, Stratakis CA. Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation [Internet]. Molecular and Cellular Endocrinology. 2021 ; 15[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.mce.2020.111117
Vancouver
Leal LF, Szarek E, Berthon A, Nesterova M, Faucz FR, London E, Mercier C, Abu-Asab M, Starost MF, Dye L, Bilinska B, Kotula-Balak M, Antonini SRR, Stratakis CA. Pde8b haploinsufficiency in mice is associated with modest adrenal defects, impaired steroidogenesis, and male infertility, unaltered by concurrent PKA or Wnt activation [Internet]. Molecular and Cellular Endocrinology. 2021 ; 15[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.mce.2020.111117

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