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Artigo de periodico
Vitamin D receptor hypermethylation as a biomarker for pediatric adrenocortical tumors (2022)
Bueno, Ana Carolina; Stecchini, Mônica Freire ; Marrero Gutierrez, Junier; More, Candy Christie Bellido ; Leal, Letícia Ferro; Gomes, Debora Cristiane; Lima Neto, Daniel Ferreira de; Brandalise, Silvia Regina; Cardinalli, Izilda Aparecida; Yunes, Jose Andres; Junqueira, Thaís; Scrideli, Carlos Alberto ; Molina, Carlos Augusto Fernandes ; Ramalho, Fernando Silva ; Tucci Júnior, Silvio ; Coeli-Lacchini, Fernanda Borchers; Moreira, Ayrton Custódio; Ramalho, Leandra Naira Zambelli ; Vêncio, Ricardo Zorzetto Nicoliello ; Castro, Margaret de ; Antonini, Sonir Roberto Rauber
Fonte: European Journal of Endocrinology. Unidades: FMRP, FFCLRP
Assuntos: BIOMARCADORES, CÓRTEX ADRENAL, METILAÇÃO, NEOPLASIAS, PEDIATRIA, RECEPTORES, VITAMINA D
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ABNT
BUENO, Ana Carolina et al. Vitamin D receptor hypermethylation as a biomarker for pediatric adrenocortical tumors. European Journal of Endocrinology, v. 186, n. 5, p. 573-585, 2022Tradução . . Disponível em: https://doi.org/10.1530/EJE-21-0879. Acesso em: 05 set. 2024.
APA
Bueno, A. C., Stecchini, M. F., Marrero Gutierrez, J., More, C. C. B., Leal, L. F., Gomes, D. C., et al. (2022). Vitamin D receptor hypermethylation as a biomarker for pediatric adrenocortical tumors. European Journal of Endocrinology, 186( 5), 573-585. doi:10.1530/EJE-21-0879
NLM
Bueno AC, Stecchini MF, Marrero Gutierrez J, More CCB, Leal LF, Gomes DC, Lima Neto DF de, Brandalise SR, Cardinalli IA, Yunes JA, Junqueira T, Scrideli CA, Molina CAF, Ramalho FS, Tucci Júnior S, Coeli-Lacchini FB, Moreira AC, Ramalho LNZ, Vêncio RZN, Castro M de, Antonini SRR. Vitamin D receptor hypermethylation as a biomarker for pediatric adrenocortical tumors [Internet]. European Journal of Endocrinology. 2022 ; 186( 5): 573-585.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-21-0879
Vancouver
Bueno AC, Stecchini MF, Marrero Gutierrez J, More CCB, Leal LF, Gomes DC, Lima Neto DF de, Brandalise SR, Cardinalli IA, Yunes JA, Junqueira T, Scrideli CA, Molina CAF, Ramalho FS, Tucci Júnior S, Coeli-Lacchini FB, Moreira AC, Ramalho LNZ, Vêncio RZN, Castro M de, Antonini SRR. Vitamin D receptor hypermethylation as a biomarker for pediatric adrenocortical tumors [Internet]. European Journal of Endocrinology. 2022 ; 186( 5): 573-585.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-21-0879
Artigo de periodico
Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome (2018)
Moreira, Ayrton Custódio; Antonini, Sonir Roberto Rauber ; Castro, Margaret de
Fonte: European Journal of Endocrinology. Unidade: FMRP
Assuntos: HORMÔNIOS GLICOCORTICOIDES, SISTEMA HIPOTÁLAMO-HIPOFISÁRIO, RITMO CIRCADIANO
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ABNT
MOREIRA, Ayrton Custódio e ANTONINI, Sonir Roberto Rauber e CASTRO, Margaret de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome. European Journal of Endocrinology, v. 179, n. 1, p. R1-R18, 2018Tradução . . Disponível em: https://doi.org/10.1530/eje-18-0102. Acesso em: 05 set. 2024.
APA
Moreira, A. C., Antonini, S. R. R., & Castro, M. de. (2018). Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome. European Journal of Endocrinology, 179( 1), R1-R18. doi:10.1530/eje-18-0102
NLM
Moreira AC, Antonini SRR, Castro M de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome [Internet]. European Journal of Endocrinology. 2018 ; 179( 1): R1-R18.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-18-0102
Vancouver
Moreira AC, Antonini SRR, Castro M de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome [Internet]. European Journal of Endocrinology. 2018 ; 179( 1): R1-R18.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-18-0102
Artigo de periodico
Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus (2017)
Araújo, Iana M. de; Salmon, Carlos Ernesto Garrido; Nahas, Andressa K.; Nogueira-Barbosa, Marcello Henrique; Elias Júnior, Jorge; Paula, Francisco Jose Albuquerque de
Fonte: European Journal of Endocrinology. Unidades: FFCLRP, FMRP
Assuntos: DIABETES MELLITUS, OBESIDADE, INSULINA, DENSIDADE ÓSSEA, TECIDO ADIPOSO
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ABNT
ARAÚJO, Iana M. de et al. Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus. European Journal of Endocrinology, v. 176, n. 1, p. 21-30, 2017Tradução . . Disponível em: https://doi.org/10.1530/EJE-16-0448. Acesso em: 05 set. 2024.
APA
Araújo, I. M. de, Salmon, C. E. G., Nahas, A. K., Nogueira-Barbosa, M. H., Elias Júnior, J., & Paula, F. J. A. de. (2017). Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus. European Journal of Endocrinology, 176( 1), 21-30. doi:10.1530/EJE-16-0448
NLM
Araújo IM de, Salmon CEG, Nahas AK, Nogueira-Barbosa MH, Elias Júnior J, Paula FJA de. Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus [Internet]. European Journal of Endocrinology. 2017 ; 176( 1): 21-30.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-16-0448
Vancouver
Araújo IM de, Salmon CEG, Nahas AK, Nogueira-Barbosa MH, Elias Júnior J, Paula FJA de. Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus [Internet]. European Journal of Endocrinology. 2017 ; 176( 1): 21-30.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-16-0448
Artigo de periodico
Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies (2017)
Yance, V. R. V.; Marcondes, J. A. M.; Rocha, M. P.; Barcellos, C. R. G.; Dantas, W. S.; Avila, A. F. A.; Baroni, R. H.; Carvalho, F. M.; Hayashida, S. A. Y.; Mendonca, B. B.; Domenice, S.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: NEOPLASIAS DOS GENITAIS FEMININOS, MENOPAUSA, HORMÔNIOS SEXUAIS, MULHERES
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ABNT
YANCE, V. R. V. et al. Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies. European Journal of Endocrinology, v. 177, n. 1, p. 93-102, 2017Tradução . . Disponível em: https://doi.org/10.1530/EJE-17-0111. Acesso em: 05 set. 2024.
APA
Yance, V. R. V., Marcondes, J. A. M., Rocha, M. P., Barcellos, C. R. G., Dantas, W. S., Avila, A. F. A., et al. (2017). Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies. European Journal of Endocrinology, 177( 1), 93-102. doi:10.1530/EJE-17-0111
NLM
Yance VRV, Marcondes JAM, Rocha MP, Barcellos CRG, Dantas WS, Avila AFA, Baroni RH, Carvalho FM, Hayashida SAY, Mendonca BB, Domenice S. Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies [Internet]. European Journal of Endocrinology. 2017 ; 177( 1): 93-102.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-17-0111
Vancouver
Yance VRV, Marcondes JAM, Rocha MP, Barcellos CRG, Dantas WS, Avila AFA, Baroni RH, Carvalho FM, Hayashida SAY, Mendonca BB, Domenice S. Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies [Internet]. European Journal of Endocrinology. 2017 ; 177( 1): 93-102.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-17-0111
Artigo de periodico
Management of endocrine disease: Diagnostic and therapeutic approach of tall stature (2017)
Albuquerque, Edoarda V. A.; Scalco, Renata C; Jorge, Alexander A. L.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: ESTATURA, ADOLESCENTES, AVALIAÇÃO EM SAÚDE, HORMÔNIOS SEXUAIS
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ABNT
ALBUQUERQUE, Edoarda V. A. e SCALCO, Renata C e JORGE, Alexander A. L. Management of endocrine disease: Diagnostic and therapeutic approach of tall stature. European Journal of Endocrinology, v. 176, n. 6, p. R339-R353, 2017Tradução . . Disponível em: https://doi.org/10.1530/EJE-16-1054. Acesso em: 05 set. 2024.
APA
Albuquerque, E. V. A., Scalco, R. C., & Jorge, A. A. L. (2017). Management of endocrine disease: Diagnostic and therapeutic approach of tall stature. European Journal of Endocrinology, 176( 6), R339-R353. doi:10.1530/EJE-16-1054
NLM
Albuquerque EVA, Scalco RC, Jorge AAL. Management of endocrine disease: Diagnostic and therapeutic approach of tall stature [Internet]. European Journal of Endocrinology. 2017 ; 176( 6): R339-R353.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-16-1054
Vancouver
Albuquerque EVA, Scalco RC, Jorge AAL. Management of endocrine disease: Diagnostic and therapeutic approach of tall stature [Internet]. European Journal of Endocrinology. 2017 ; 176( 6): R339-R353.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-16-1054
Artigo de periodico
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability (2015)
Scalco, Renata C.; Hwa, Vivian; Domené, Horacio M.; Jasper, Héctor G.; Belgorosky, Alicia; Marino, Roxana; Pereira, Alberto M.; Tonelli, Carlos A.; Wit, Jan M.; Rosenfeld, Ron G.; Jorge, Alexander A. L.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: PREVALÊNCIA, SEQUÊNCIA DO DNA, MUTAÇÃO GENÉTICA, DOENÇAS HEREDITÁRIAS
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ABNT
SCALCO, Renata C. et al. STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability. European Journal of Endocrinology, v. 173, n. 3, p. 291-296, 2015Tradução . . Disponível em: https://doi.org/10.1530/EJE-15-0398. Acesso em: 05 set. 2024.
APA
Scalco, R. C., Hwa, V., Domené, H. M., Jasper, H. G., Belgorosky, A., Marino, R., et al. (2015). STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability. European Journal of Endocrinology, 173( 3), 291-296. doi:10.1530/EJE-15-0398
NLM
Scalco RC, Hwa V, Domené HM, Jasper HG, Belgorosky A, Marino R, Pereira AM, Tonelli CA, Wit JM, Rosenfeld RG, Jorge AAL. STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability [Internet]. European Journal of Endocrinology. 2015 ; 173( 3): 291-296.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-15-0398
Vancouver
Scalco RC, Hwa V, Domené HM, Jasper HG, Belgorosky A, Marino R, Pereira AM, Tonelli CA, Wit JM, Rosenfeld RG, Jorge AAL. STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability [Internet]. European Journal of Endocrinology. 2015 ; 173( 3): 291-296.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-15-0398
Artigo de periodico
Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma (2014)
Danilovic, Debora L. S.; Lima, Erika U.; Domingues, Regina B.; Brandao, Lenine G.; Hoff, Ana O.; Marui, Suemi
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, NEOPLASIAS DA TIREOIDE (DIAGNÓSTICO), PROGNÓSTICO, CARCINOMA DE CÉLULAS ESCAMOSAS
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ABNT
DANILOVIC, Debora L. S. et al. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, v. 170, n. 4, p. 619-625, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-13-0944. Acesso em: 05 set. 2024.
APA
Danilovic, D. L. S., Lima, E. U., Domingues, R. B., Brandao, L. G., Hoff, A. O., & Marui, S. (2014). Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, 170( 4), 619-625. doi:10.1530/EJE-13-0944
NLM
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-13-0944
Vancouver
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-13-0944
Artigo de periodico
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations (2014)
Longuini, Viviane Cristina; Lourenço Júnior, Delmar M; Sekiya, Tomoko; Meirelles, Osorio; Goncalves, Tatiana D.; Coutinho, Flavia L.; Francisco, Guilherme; Osaki, Luciana H.; Chammas, Roger; Alves, Venâncio Avancini Ferreira; Siqueira, Sheila A. C.; Schlesinger, David; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lucia; Gama, Patrícia ; Lee, Misu; Molatore, Sara; Pereira, Maria Adelaide A.; Jallad, Raquel S.; Bronstein, Marcello D.; Cunha-Neto, Malebranche B.; Liberman, Bernardo; Fragoso, Maria Candida B. V.; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo A.
Fonte: European Journal of Endocrinology. Unidades: FM, IB, EE, FSP, ICB
Assuntos: MUTAÇÃO GENÉTICA, GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA
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ABNT
LONGUINI, Viviane Cristina et al. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, n. Ju 2014, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0130. Acesso em: 05 set. 2024.
APA
Longuini, V. C., Lourenço Júnior, D. M., Sekiya, T., Meirelles, O., Goncalves, T. D., Coutinho, F. L., et al. (2014). Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, ( Ju 2014). doi:10.1530/EJE-14-0130
NLM
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-14-0130
Vancouver
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-14-0130
Artigo de periodico
Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways (2014)
Canton, Ana P. M.; Costa, Sílvia S.; Rodrigues, Tatiane C.; Bertola, Debora R.; Malaquias, Alexsandra C.; Correa, Fernanda A.; Arnhold, Ivo J. P.; Rosenberg, Carla ; Jorge, Alexander A. L.
Fonte: European Journal of Endocrinology. Unidades: IB, FM
Assuntos: GENES, IDADE GESTACIONAL, CRESCIMENTO E DESENVOLVIMENTO
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ABNT
CANTON, Ana P. M. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, v. 171, n. 2, p. 253-262, 2014Tradução . . Disponível em: https://doi.org/10.1530/eje-14-0232. Acesso em: 05 set. 2024.
APA
Canton, A. P. M., Costa, S. S., Rodrigues, T. C., Bertola, D. R., Malaquias, A. C., Correa, F. A., et al. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology, 171( 2), 253-262. doi:10.1530/eje-14-0232
NLM
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-14-0232
Vancouver
Canton APM, Costa SS, Rodrigues TC, Bertola DR, Malaquias AC, Correa FA, Arnhold IJP, Rosenberg C, Jorge AAL. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways [Internet]. European Journal of Endocrinology. 2014 ; 171( 2): 253-262.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-14-0232
Artigo de periodico
Role of RET genetic variants in MEN2-associated pheochromocytoma (2014)
Siqueira, Débora Rodrigues; Ceolin, Luciele; Ferreira, Carla Vaz; Romitti, Mírian; Maia, Silvana Cavalcante; Maciel, Léa Maria Zanini; Maia, Ana Luiza
Fonte: European Journal of Endocrinology. Unidade: FMRP
Assuntos: NEOPLASIAS EPITELIAIS E GLANDULARES, NEOPLASIA ENDÓCRINA MÚLTIPLA, FEOCROMOCITOMA, POLIMORFISMO, PROTEÍNAS PROTO-ONCOGÊNICAS
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ABNT
SIQUEIRA, Débora Rodrigues et al. Role of RET genetic variants in MEN2-associated pheochromocytoma. European Journal of Endocrinology, v. 170, n. 6, p. 821-828, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0084. Acesso em: 05 set. 2024.
APA
Siqueira, D. R., Ceolin, L., Ferreira, C. V., Romitti, M., Maia, S. C., Maciel, L. M. Z., & Maia, A. L. (2014). Role of RET genetic variants in MEN2-associated pheochromocytoma. European Journal of Endocrinology, 170( 6), 821-828. doi:10.1530/EJE-14-0084
NLM
Siqueira DR, Ceolin L, Ferreira CV, Romitti M, Maia SC, Maciel LMZ, Maia AL. Role of RET genetic variants in MEN2-associated pheochromocytoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 6): 821-828.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-14-0084
Vancouver
Siqueira DR, Ceolin L, Ferreira CV, Romitti M, Maia SC, Maciel LMZ, Maia AL. Role of RET genetic variants in MEN2-associated pheochromocytoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 6): 821-828.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-14-0084
Artigo de periodico
The cortisol awakening response is blunted in patients with active Cushing's disease (2013)
Roa, Silvia Liliana Ruiz; Elias, Paula Conde Lamparelli; Castro, Margaret de; Moreira, Ayrton Custódio
Fonte: European Journal of Endocrinology. Unidade: FMRP
Assuntos: CORTISOL, RITMO CIRCADIANO, GLÂNDULA PITUITÁRIA
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ABNT
ROA, Silvia Liliana Ruiz et al. The cortisol awakening response is blunted in patients with active Cushing's disease. European Journal of Endocrinology, v. 168, n. 5, p. 657-664, 2013Tradução . . Disponível em: https://doi.org/10.1530/EJE-12-0982. Acesso em: 05 set. 2024.
APA
Roa, S. L. R., Elias, P. C. L., Castro, M. de, & Moreira, A. C. (2013). The cortisol awakening response is blunted in patients with active Cushing's disease. European Journal of Endocrinology, 168( 5), 657-664. doi:10.1530/EJE-12-0982
NLM
Roa SLR, Elias PCL, Castro M de, Moreira AC. The cortisol awakening response is blunted in patients with active Cushing's disease [Internet]. European Journal of Endocrinology. 2013 ; 168( 5): 657-664.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-12-0982
Vancouver
Roa SLR, Elias PCL, Castro M de, Moreira AC. The cortisol awakening response is blunted in patients with active Cushing's disease [Internet]. European Journal of Endocrinology. 2013 ; 168( 5): 657-664.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-12-0982
Artigo de periodico
Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients (2012)
Fragoso, Maria Candida B. V.; Almeida, Madson Queiroz; Mazzuco, Tania L.; Mariani, Beatriz M. P.; Brito, Luciana P.; Gonçalves, Talita Cardoso; Alencar, Guilherme A.; Lima, Lorena de O.; Faria, Andre M.; Bourdeau, Isabelle; Lucon, Antonio M.; Freire, Daniel S.; Latronico, Ana Claudia; Mendonca, Berenice B.; Lacroix, Andre; Lerario, Antonio M.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, PROGNÓSTICO, CRIANÇAS, ADULTOS, EXPRESSÃO GÊNICA, ESTUDOS DE COORTES, BRASIL
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ABNT
FRAGOSO, Maria Candida B. V. et al. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, v. 166, n. 1, p. 61-67, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 05 set. 2024.
APA
Fragoso, M. C. B. V., Almeida, M. Q., Mazzuco, T. L., Mariani, B. M. P., Brito, L. P., Gonçalves, T. C., et al. (2012). Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, 166( 1), 61-67. doi:10.1530/EJE-11-0964
NLM
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico
Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 (2012)
Montenegro, Luciana R.; Leal, Andrea C.; Coutinho, Debora C.; Valassi, Helena P. L.; Nishi, Mirian Y.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Jorge, Alexander A. L.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: METABOLISMO (QUÍMICA), PROLIFERAÇÃO CELULAR, CULTURA DE CÉLULAS, FENÓTIPOS, REAÇÃO EM CADEIA POR POLIMERASE, ANORMALIDADES MUSCULOSQUELÉTICAS (GENÉTICA), BIOQUÍMICA CLÍNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTENEGRO, Luciana R. et al. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, v. 166, n. 3, p. 543-550, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 05 set. 2024.
APA
Montenegro, L. R., Leal, A. C., Coutinho, D. C., Valassi, H. P. L., Nishi, M. Y., Arnhold, I. J. P., et al. (2012). Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, 166( 3), 543-550. doi:10.1530/EJE-11-0964
NLM
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico
SAGE analysis highlights the putative role of underexpression of ribosomal proteins in GH-secreting pituitary adenomas (2012)
Lima, Deison Soares de; Martins, Clarissa Silva; Paixão, Beatriz Maria de Carvalho; Amaral, Fernando Colbari; Colli, Leandro Machado; Saggioro, Fabiano Pinto; Neder, Luciano; Machado, Hélio Rubens; Santos, Anemari Ramos Dinarte dos; Pinheiro, Daniel G.; Moreira, Ayrton Custódio; Silva Júnior, Wilson Araújo da; Castro, Margaret de
Fonte: European Journal of Endocrinology. Unidades: SVOI, FMRP
Assuntos: EXPRESSÃO GÊNICA, GLÂNDULA PITUITÁRIA, ADENOMA, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Deison Soares de et al. SAGE analysis highlights the putative role of underexpression of ribosomal proteins in GH-secreting pituitary adenomas. European Journal of Endocrinology, v. 167, n. 6, p. 759-768, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-12-0760. Acesso em: 05 set. 2024.
APA
Lima, D. S. de, Martins, C. S., Paixão, B. M. de C., Amaral, F. C., Colli, L. M., Saggioro, F. P., et al. (2012). SAGE analysis highlights the putative role of underexpression of ribosomal proteins in GH-secreting pituitary adenomas. European Journal of Endocrinology, 167( 6), 759-768. doi:10.1530/EJE-12-0760
NLM
Lima DS de, Martins CS, Paixão BM de C, Amaral FC, Colli LM, Saggioro FP, Neder L, Machado HR, Santos ARD dos, Pinheiro DG, Moreira AC, Silva Júnior WA da, Castro M de. SAGE analysis highlights the putative role of underexpression of ribosomal proteins in GH-secreting pituitary adenomas [Internet]. European Journal of Endocrinology. 2012 ; 167( 6): 759-768.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-12-0760
Vancouver
Lima DS de, Martins CS, Paixão BM de C, Amaral FC, Colli LM, Saggioro FP, Neder L, Machado HR, Santos ARD dos, Pinheiro DG, Moreira AC, Silva Júnior WA da, Castro M de. SAGE analysis highlights the putative role of underexpression of ribosomal proteins in GH-secreting pituitary adenomas [Internet]. European Journal of Endocrinology. 2012 ; 167( 6): 759-768.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-12-0760
Artigo de periodico
Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism (2011)
Beneduzzi, Daiane; Iyer, Anita K.; Trarbach, Ericka Barbosa; Silveira-Neto, Acacio P.; Silveira, Letícia G.; Tusset, Cintia; Yip, Kathleen; Mendonça, Berenice B,; Mellon, Pamela L.; Latronico, Ana Claudia
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: HIPOGONADISMO (GENÉTICO;CONGÊNITO), PUBERDADE (DESENVOLVIMENTO), HORMÔNIO LUTEINIZANTE (SECREÇÃO), HIPOTÁLAMO (FISIOPATOLOGIA), GENES, HORMÔNIO FOLÍCULO-ESTIMULANTE (SECREÇÃO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BENEDUZZI, Daiane et al. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 165, n. 2, p. 145-150, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0199. Acesso em: 05 set. 2024.
APA
Beneduzzi, D., Iyer, A. K., Trarbach, E. B., Silveira-Neto, A. P., Silveira, L. G., Tusset, C., et al. (2011). Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 165( 2), 145-150. doi:10.1530/EJE-11-0199
NLM
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0199
Vancouver
Beneduzzi D, Iyer AK, Trarbach EB, Silveira-Neto AP, Silveira LG, Tusset C, Yip K, Mendonça BB, Mellon PL, Latronico AC. Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2011 ; 165( 2): 145-150.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-11-0199
Artigo de periodico
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism (2010)
Teles, M. G.; Trarbach, E. B.; Noel, S. D.; Guerra Junior, G.; Beneduzzi, D.; Bianco, S. D.; Jorge, Alexander A. L.; Mukherjee, A.; Baptista, M. T.; Costa, E. M.; Castro, M. de; Mendonça, B. B.; Kaiser, U. B.; Latronico, A. C.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA), MUTAÇÃO GENÉTICA, DOENÇAS PULMONARES INTERSTICIAIS, SISTEMA IMUNE (FISIOPATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TELES, M. G. et al. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 163, n. 1, p. 29-34, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0012. Acesso em: 05 set. 2024.
APA
Teles, M. G., Trarbach, E. B., Noel, S. D., Guerra Junior, G., Beneduzzi, D., Bianco, S. D., et al. (2010). A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 163( 1), 29-34. doi:10.1530/EJE-10-0012
NLM
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-10-0012
Vancouver
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-10-0012
Artigo de periodico
Subclinical thyroid dysfunctions are independent risk factors for mortality in a 7.5-year follow-up: the Japanese-Brazilian thyroid study (2010)
Sgarbi, José Augusto; Matsumura, Luiza Kimiko; Kasamatsu, Teresa Sayoko; Vivolo, Sandra Roberta Gouvea Ferreira; Maciel, Rui Monteiro de Barros
Fonte: European Journal of Endocrinology. Unidade: FSP
Assuntos: HIPERTIREOIDISMO (PREVALÊNCIA), HIPOTIREOIDISMO (PREVALÊNCIA), DOENÇAS CARDIOVASCULARES (RELAÇÃO), NIPO-BRASILEIROS, EPIDEMIOLOGIA ANALÍTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SGARBI, José Augusto et al. Subclinical thyroid dysfunctions are independent risk factors for mortality in a 7.5-year follow-up: the Japanese-Brazilian thyroid study. European Journal of Endocrinology, v. 162, n. 3, p. 569-577, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-09-0845. Acesso em: 05 set. 2024.
APA
Sgarbi, J. A., Matsumura, L. K., Kasamatsu, T. S., Vivolo, S. R. G. F., & Maciel, R. M. de B. (2010). Subclinical thyroid dysfunctions are independent risk factors for mortality in a 7.5-year follow-up: the Japanese-Brazilian thyroid study. European Journal of Endocrinology, 162( 3), 569-577. doi:10.1530/EJE-09-0845
NLM
Sgarbi JA, Matsumura LK, Kasamatsu TS, Vivolo SRGF, Maciel RM de B. Subclinical thyroid dysfunctions are independent risk factors for mortality in a 7.5-year follow-up: the Japanese-Brazilian thyroid study [Internet]. European Journal of Endocrinology. 2010 ; 162( 3): 569-577.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-09-0845
Vancouver
Sgarbi JA, Matsumura LK, Kasamatsu TS, Vivolo SRGF, Maciel RM de B. Subclinical thyroid dysfunctions are independent risk factors for mortality in a 7.5-year follow-up: the Japanese-Brazilian thyroid study [Internet]. European Journal of Endocrinology. 2010 ; 162( 3): 569-577.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-09-0845
Artigo de periodico
Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age (2010)
Bueno, Ana Carolina; Espiñeira, Aniette R.; Fernandes-Rosa, Fábio L.; Souza, Roberto Molina de; Castro, Margaret de; Moreira, Ayrton Custódio; Bettiol, Heloisa; Barbieri, Marco Antonio; Antonini, Sonir Roberto Rauber
Fonte: European Journal of Endocrinology. Unidade: FMRP
Assuntos: POLIMORFISMO, BEBÊS, ADIPONECTINA
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ABNT
BUENO, Ana Carolina et al. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age. European Journal of Endocrinology, v. 162, n. 1, p. 53-60, 2010Tradução . . Disponível em: https://doi.org/10.1530/eje-09-0697. Acesso em: 05 set. 2024.
APA
Bueno, A. C., Espiñeira, A. R., Fernandes-Rosa, F. L., Souza, R. M. de, Castro, M. de, Moreira, A. C., et al. (2010). Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age. European Journal of Endocrinology, 162( 1), 53-60. doi:10.1530/eje-09-0697
NLM
Bueno AC, Espiñeira AR, Fernandes-Rosa FL, Souza RM de, Castro M de, Moreira AC, Bettiol H, Barbieri MA, Antonini SRR. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age [Internet]. European Journal of Endocrinology. 2010 ; 162( 1): 53-60.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-09-0697
Vancouver
Bueno AC, Espiñeira AR, Fernandes-Rosa FL, Souza RM de, Castro M de, Moreira AC, Bettiol H, Barbieri MA, Antonini SRR. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age [Internet]. European Journal of Endocrinology. 2010 ; 162( 1): 53-60.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-09-0697
Artigo de periodico
A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings (2010)
Pires, Patricia N. Pugliese; Tonelli, Carlos A.; Dora, Jose M.; Silva, Paulo C. A.; Czepielewski, Mauro; Simoni, Genoir; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA), MUTAÇÃO GENÉTICA, DOENÇAS PULMONARES INTERSTICIAIS, SISTEMA IMUNE (FISIOPATOLOGIA), PROLACTINA (FISIOPATOLOGIA)
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ABNT
PIRES, Patricia N. Pugliese et al. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, v. 163, n. 2, p. 349-355, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0272. Acesso em: 05 set. 2024.
APA
Pires, P. N. P., Tonelli, C. A., Dora, J. M., Silva, P. C. A., Czepielewski, M., Simoni, G., et al. (2010). A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, 163( 2), 349-355. doi:10.1530/EJE-10-0272
NLM
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-10-0272
Vancouver
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/EJE-10-0272
Artigo de periodico
Heterogeneity in the molecular basis of ACTH resistance syndrome (2008)
Collares, Cristhiana Viesti Advincula; Antunes-Rodrigues, José; Moreira, Ayrton Custódio; Franca, Suzana Nesi; Pereira, Luiz Alberto; Soares, Maria Marta Sarquis; Elias Júnior, Jorge; Clark, Adrian J.; Castro, Margaret de; Elias, Lucila Leico Kagohara
Fonte: European Journal of Endocrinology. Unidade: FMRP
Assuntos: ENDOCRINOLOGIA, DOENÇAS METABÓLICAS
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ABNT
COLLARES, Cristhiana Viesti Advincula et al. Heterogeneity in the molecular basis of ACTH resistance syndrome. European Journal of Endocrinology, v. 159, n. 1, p. 61-68, 2008Tradução . . Disponível em: https://doi.org/10.1530/eje-08-0079. Acesso em: 05 set. 2024.
APA
Collares, C. V. A., Antunes-Rodrigues, J., Moreira, A. C., Franca, S. N., Pereira, L. A., Soares, M. M. S., et al. (2008). Heterogeneity in the molecular basis of ACTH resistance syndrome. European Journal of Endocrinology, 159( 1), 61-68. doi:10.1530/eje-08-0079
NLM
Collares CVA, Antunes-Rodrigues J, Moreira AC, Franca SN, Pereira LA, Soares MMS, Elias Júnior J, Clark AJ, Castro M de, Elias LLK. Heterogeneity in the molecular basis of ACTH resistance syndrome [Internet]. European Journal of Endocrinology. 2008 ; 159( 1): 61-68.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-08-0079
Vancouver
Collares CVA, Antunes-Rodrigues J, Moreira AC, Franca SN, Pereira LA, Soares MMS, Elias Júnior J, Clark AJ, Castro M de, Elias LLK. Heterogeneity in the molecular basis of ACTH resistance syndrome [Internet]. European Journal of Endocrinology. 2008 ; 159( 1): 61-68.[citado 2024 set. 05 ] Available from: https://doi.org/10.1530/eje-08-0079

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