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Artigo de periodico
Peripheral clock system circadian abnormalities in Cushing’s disease (2020)
Soares, Vinicius Reis; Martins, Clarissa Silva ; Martinez, Edson Zangiacomi ; Araújo, Leonardo Domingues de ; Roa, Silvia Liliana Ruiz; Silva, Lucas Ravagnani; Moreira, Ayrton Custódio ; Castro, Margaret de
Source: Chronobiology International. Unidade: FMRP
Subjects: HORMÔNIO ADRENOCORTICOTRÓFICO, HORMÔNIOS GLICOCORTICOIDES, RITMO CIRCADIANO
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ABNT
SOARES, Vinicius Reis et al. Peripheral clock system circadian abnormalities in Cushing’s disease. Chronobiology International, v. 37, n. 6, p. 867-876, 2020Tradução . . Disponível em: https://doi.org/10.1080/07420528.2020.1758126. Acesso em: 16 nov. 2024.
APA
Soares, V. R., Martins, C. S., Martinez, E. Z., Araújo, L. D. de, Roa, S. L. R., Silva, L. R., et al. (2020). Peripheral clock system circadian abnormalities in Cushing’s disease. Chronobiology International, 37( 6), 867-876. doi:10.1080/07420528.2020.1758126
NLM
Soares VR, Martins CS, Martinez EZ, Araújo LD de, Roa SLR, Silva LR, Moreira AC, Castro M de. Peripheral clock system circadian abnormalities in Cushing’s disease [Internet]. Chronobiology International. 2020 ; 37( 6): 867-876.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1080/07420528.2020.1758126
Vancouver
Soares VR, Martins CS, Martinez EZ, Araújo LD de, Roa SLR, Silva LR, Moreira AC, Castro M de. Peripheral clock system circadian abnormalities in Cushing’s disease [Internet]. Chronobiology International. 2020 ; 37( 6): 867-876.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1080/07420528.2020.1758126
Trabalho de evento-resumo periodico
Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency (2019)
Bodoni, Aline F. ; Coeli-Lacchini, Fernanda Borchers ; Gebenlian, Juliana Lourenço; Sobral, Lays Martin ; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara ; Silva Junior, Wilson Araújo da ; Castro, Margaret de ; Leopoldino, Andréia Machado ; Antonini, Sonir Roberto Rauber
Source: Hormone Research in Paediatrics. Conference titles: Annual Meeting European Society for Paediatric Endocrinology - ESPE. Unidades: FMRP, FCFRP
Subjects: CORTISOL, HORMÔNIOS GLICOCORTICOIDES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BODONI, Aline F. et al. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000501868. Acesso em: 16 nov. 2024. , 2019
APA
Bodoni, A. F., Coeli-Lacchini, F. B., Gebenlian, J. L., Sobral, L. M., Moreira, A. C., Elias, L. L. K., et al. (2019). Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1159/000501868
NLM
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Moreira AC, Elias LLK, Silva Junior WA da, Castro M de, Leopoldino AM, Antonini SRR. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency [Internet]. Hormone Research in Paediatrics. 2019 ; 91 108.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1159/000501868
Vancouver
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Moreira AC, Elias LLK, Silva Junior WA da, Castro M de, Leopoldino AM, Antonini SRR. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency [Internet]. Hormone Research in Paediatrics. 2019 ; 91 108.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1159/000501868
Trabalho de evento-resumo periodico
Peripheral clock system circadian imbalance in Cushing's disease (2019)
Soares, Vinícius; Martins, Clarissa; Martinez, Edson Zangiacomi ; Araújo, Leonardo Domingues de ; Roa, Silva; Silva, Lucas; Moreira, Ayrton Custódio; Castro, Margaret de
Source: Journal of Endocrine Society. Conference titles: Annual Meeting of the Endocrine Society (ENDO). Unidade: FMRP
Subjects: EXPRESSÃO GÊNICA, LEUCÓCITOS, HORMÔNIOS GLICOCORTICOIDES, RITMO CIRCADIANO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOARES, Vinícius et al. Peripheral clock system circadian imbalance in Cushing's disease. Journal of Endocrine Society. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1210/js.2019-SUN-LB063. Acesso em: 16 nov. 2024. , 2019
APA
Soares, V., Martins, C., Martinez, E. Z., Araújo, L. D. de, Roa, S., Silva, L., et al. (2019). Peripheral clock system circadian imbalance in Cushing's disease. Journal of Endocrine Society. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1210/js.2019-SUN-LB063
NLM
Soares V, Martins C, Martinez EZ, Araújo LD de, Roa S, Silva L, Moreira AC, Castro M de. Peripheral clock system circadian imbalance in Cushing's disease [Internet]. Journal of Endocrine Society. 2019 ; 3[citado 2024 nov. 16 ] Available from: https://doi.org/10.1210/js.2019-SUN-LB063
Vancouver
Soares V, Martins C, Martinez EZ, Araújo LD de, Roa S, Silva L, Moreira AC, Castro M de. Peripheral clock system circadian imbalance in Cushing's disease [Internet]. Journal of Endocrine Society. 2019 ; 3[citado 2024 nov. 16 ] Available from: https://doi.org/10.1210/js.2019-SUN-LB063
Artigo de periodico
Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2 (2019)
Resende, Ana Teresa Prata ; Martins, Clarissa Silva ; Bueno, Ana Carolina ; Moreira, Ayrton Custódio; Foss-Freitas, Maria Cristina ; Castro, Margaret de
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: INSULINA, SÍNDROME X METABÓLICA, HORMÔNIOS GLICOCORTICOIDES, FENÓTIPOS
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ABNT
RESENDE, Ana Teresa Prata et al. Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2. Clinical Endocrinology, v. 91, n. 1, p. 94-103, 2019Tradução . . Disponível em: https://doi.org/10.1111/cen.13984. Acesso em: 16 nov. 2024.
APA
Resende, A. T. P., Martins, C. S., Bueno, A. C., Moreira, A. C., Foss-Freitas, M. C., & Castro, M. de. (2019). Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2. Clinical Endocrinology, 91( 1), 94-103. doi:10.1111/cen.13984
NLM
Resende ATP, Martins CS, Bueno AC, Moreira AC, Foss-Freitas MC, Castro M de. Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2 [Internet]. Clinical Endocrinology. 2019 ; 91( 1): 94-103.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cen.13984
Vancouver
Resende ATP, Martins CS, Bueno AC, Moreira AC, Foss-Freitas MC, Castro M de. Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2 [Internet]. Clinical Endocrinology. 2019 ; 91( 1): 94-103.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cen.13984
Artigo de periodico
A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and Metabolism (2018)
Machado, Márcio Carlos; Fragoso, Maria Candida Barisson Vilares; Moreira, Ayrton Custódio; Boguszewski, César Luiz ; Vieira Neto, Leonardo ; Naves, Luciana A.; Vilar, Lucio; Araújo, Luiz Antônio de; Musolino, Nina Rosa Castro; Miranda, Paulo Augusto C.; Czepielewski, Mauro A. ; Gadelha, Monica R. ; Bronstein, Marcello Delano ; Oliveira Junior, Antônio Ribeiro
Source: Archives of Endrocrinology and Metabolism. Unidade: FMRP
Subjects: GLÂNDULA PITUITÁRIA, HORMÔNIOS GLICOCORTICOIDES, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACHADO, Márcio Carlos et al. A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and Metabolism. Archives of Endrocrinology and Metabolism, v. 62, n. 1, p. 87-105, 2018Tradução . . Disponível em: https://doi.org/10.20945/2359-3997000000014. Acesso em: 16 nov. 2024.
APA
Machado, M. C., Fragoso, M. C. B. V., Moreira, A. C., Boguszewski, C. L., Vieira Neto, L., Naves, L. A., et al. (2018). A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and Metabolism. Archives of Endrocrinology and Metabolism, 62( 1), 87-105. doi:10.20945/2359-3997000000014
NLM
Machado MC, Fragoso MCBV, Moreira AC, Boguszewski CL, Vieira Neto L, Naves LA, Vilar L, Araújo LA de, Musolino NRC, Miranda PAC, Czepielewski MA, Gadelha MR, Bronstein MD, Oliveira Junior AR. A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and Metabolism [Internet]. Archives of Endrocrinology and Metabolism. 2018 ; 62( 1): 87-105.[citado 2024 nov. 16 ] Available from: https://doi.org/10.20945/2359-3997000000014
Vancouver
Machado MC, Fragoso MCBV, Moreira AC, Boguszewski CL, Vieira Neto L, Naves LA, Vilar L, Araújo LA de, Musolino NRC, Miranda PAC, Czepielewski MA, Gadelha MR, Bronstein MD, Oliveira Junior AR. A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and Metabolism [Internet]. Archives of Endrocrinology and Metabolism. 2018 ; 62( 1): 87-105.[citado 2024 nov. 16 ] Available from: https://doi.org/10.20945/2359-3997000000014
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
Source: European Journal of Endocrinology. Unidade: FMRP
Subjects: HORMÔNIOS GLICOCORTICOIDES, SISTEMA HIPOTÁLAMO-HIPOFISÁRIO, RITMO CIRCADIANO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1530/eje-18-0102
Trabalho de evento-resumo
Mitochondrial oxidative stress and glucocorticoid family deficiency: phenotypic and functional characterization of the new variant p.G866D in the gene Nicotinamide Nucleotide Transidrogenase (NNT) (2017)
Bodoni, A. F; Coeli-Lacchini, F. B; Sobral, L. M; Leopoldino, Andréia Machado; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara; Silva Júnior, Wilson Araújo da; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Source: Abstracts. Conference titles: Brazilian International Congress of Genetics - Genética 2017. Unidades: FMRP, FCFRP
Subjects: ESTRESSE OXIDATIVO, HORMÔNIOS GLICOCORTICOIDES, FENÓTIPOS, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BODONI, A. F et al. Mitochondrial oxidative stress and glucocorticoid family deficiency: phenotypic and functional characterization of the new variant p.G866D in the gene Nicotinamide Nucleotide Transidrogenase (NNT). 2017, Anais.. Águas de Lindóia: SBG, 2017. . Acesso em: 16 nov. 2024.
APA
Bodoni, A. F., Coeli-Lacchini, F. B., Sobral, L. M., Leopoldino, A. M., Moreira, A. C., Elias, L. L. K., et al. (2017). Mitochondrial oxidative stress and glucocorticoid family deficiency: phenotypic and functional characterization of the new variant p.G866D in the gene Nicotinamide Nucleotide Transidrogenase (NNT). In Abstracts. Águas de Lindóia: SBG.
NLM
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Mitochondrial oxidative stress and glucocorticoid family deficiency: phenotypic and functional characterization of the new variant p.G866D in the gene Nicotinamide Nucleotide Transidrogenase (NNT). Abstracts. 2017 ;[citado 2024 nov. 16 ]
Vancouver
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Mitochondrial oxidative stress and glucocorticoid family deficiency: phenotypic and functional characterization of the new variant p.G866D in the gene Nicotinamide Nucleotide Transidrogenase (NNT). Abstracts. 2017 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells (2015)
Bodoni, A. F.; Coeli-Lacchini, F. B.; Sobral, L. M.; Leopoldino, Andréia Machado; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara; Silva Júnior, Wilson Araújo da; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidades: FMRP, FCFRP
Subjects: HORMÔNIOS GLICOCORTICOIDES, FENÓTIPOS, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BODONI, A. F. et al. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. 2015, Anais.. Águas de Lindóia: SBG, 2015. . Acesso em: 16 nov. 2024.
APA
Bodoni, A. F., Coeli-Lacchini, F. B., Sobral, L. M., Leopoldino, A. M., Moreira, A. C., Elias, L. L. K., et al. (2015). Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. In Abstracts. Águas de Lindóia: SBG.
NLM
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Vancouver
Bodoni AF, Coeli-Lacchini FB, Sobral LM, Leopoldino AM, Moreira AC, Elias LLK, Silva Júnior WA da, Castro M de, Antonini SRR. Novel mutation P.G866D in NNT gene found in family deficiency glucocorticoids change oxidative state of mononuclear cells. Abstracts. 2015 ;[citado 2024 nov. 16 ]

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