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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
Source: European Journal of Endocrinology. Unidade: FMRP
Subjects: 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: 30 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. 30 ] 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. 30 ] Available from: https://doi.org/10.1530/eje-08-0079
Artigo de periodico
The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony (2007)
Custódio, Rodrigo José; Martinelli Júnior, Carlos Eduardo; Milani, Soraya Lopes Sader; Simões, Aguinaldo Luiz; Castro, Margaret de; Moreira, Ayrton Custódio
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: RITMO CIRCADIANO, GÊMEOS, PEDIATRIA
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ABNT
CUSTÓDIO, Rodrigo José et al. The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony. Clinical Endocrinology, v. 66, n. 2, p. 192-197, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02706.x. Acesso em: 30 set. 2024.
APA
Custódio, R. J., Martinelli Júnior, C. E., Milani, S. L. S., Simões, A. L., Castro, M. de, & Moreira, A. C. (2007). The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony. Clinical Endocrinology, 66( 2), 192-197. doi:10.1111/j.1365-2265.2006.02706.x
NLM
Custódio RJ, Martinelli Júnior CE, Milani SLS, Simões AL, Castro M de, Moreira AC. The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony [Internet]. Clinical Endocrinology. 2007 ; 66( 2): 192-197.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02706.x
Vancouver
Custódio RJ, Martinelli Júnior CE, Milani SLS, Simões AL, Castro M de, Moreira AC. The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony [Internet]. Clinical Endocrinology. 2007 ; 66( 2): 192-197.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02706.x
Artigo de periodico
Hypothalamic-pituitary-adrenal axis up-regulation in rats submitted to pituitary stalk compression (2004)
Elias, Paula Conde Lamparelli; Elias, Lucila Leico Kagohara; Castro, Margaret de; Antunes-Rodrigues, José; Moreira, Ayrton Custódio
Source: Journal of Endocrinology. Unidade: FMRP
Assunto: NEUROENDOCRINOLOGIA
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ABNT
ELIAS, Paula Conde Lamparelli et al. Hypothalamic-pituitary-adrenal axis up-regulation in rats submitted to pituitary stalk compression. Journal of Endocrinology, v. 180, p. 297-302, 2004Tradução . . Disponível em: https://doi.org/10.1677/joe.0.1800297. Acesso em: 30 set. 2024.
APA
Elias, P. C. L., Elias, L. L. K., Castro, M. de, Antunes-Rodrigues, J., & Moreira, A. C. (2004). Hypothalamic-pituitary-adrenal axis up-regulation in rats submitted to pituitary stalk compression. Journal of Endocrinology, 180, 297-302. doi:10.1677/joe.0.1800297
NLM
Elias PCL, Elias LLK, Castro M de, Antunes-Rodrigues J, Moreira AC. Hypothalamic-pituitary-adrenal axis up-regulation in rats submitted to pituitary stalk compression [Internet]. Journal of Endocrinology. 2004 ; 180 297-302.[citado 2024 set. 30 ] Available from: https://doi.org/10.1677/joe.0.1800297
Vancouver
Elias PCL, Elias LLK, Castro M de, Antunes-Rodrigues J, Moreira AC. Hypothalamic-pituitary-adrenal axis up-regulation in rats submitted to pituitary stalk compression [Internet]. Journal of Endocrinology. 2004 ; 180 297-302.[citado 2024 set. 30 ] Available from: https://doi.org/10.1677/joe.0.1800297
Artigo de periodico
Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene (2003)
Elias, Paula Conde Lamparelli; Elias, Lucila Leico Kagohara; Torres, Natalia; Moreira, Ayrton Custódio; Antunes-Rodrigues, José; Castro, Margaret de
Source: Clinical Endocrinology. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ELIAS, Paula Conde Lamparelli et al. Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene. Clinical Endocrinology, v. 39, p. 511-518, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2003.01834.x. Acesso em: 30 set. 2024.
APA
Elias, P. C. L., Elias, L. L. K., Torres, N., Moreira, A. C., Antunes-Rodrigues, J., & Castro, M. de. (2003). Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene. Clinical Endocrinology, 39, 511-518. doi:10.1046/j.1365-2265.2003.01834.x
NLM
Elias PCL, Elias LLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene [Internet]. Clinical Endocrinology. 2003 ; 39 511-518.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01834.x
Vancouver
Elias PCL, Elias LLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene [Internet]. Clinical Endocrinology. 2003 ; 39 511-518.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01834.x
Artigo de periodico
Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls (2000)
Marui, S.; Castro, Margaret de; Latronico, A. C.; Elias, Lucila Leico Kagohara; Arnhold, Ivo Jorge Prado; Moreira, Ayrton Custódio; Mendonça, B. B.
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOLOGIA, HORMÔNIOS (METABOLISMO), DESENVOLVIMENTO FÍSICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARUI, S. et al. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls. Clinical Endocrinology, v. 52, p. 67-75, 2000Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2000.00873.x. Acesso em: 30 set. 2024.
APA
Marui, S., Castro, M. de, Latronico, A. C., Elias, L. L. K., Arnhold, I. J. P., Moreira, A. C., & Mendonça, B. B. (2000). Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls. Clinical Endocrinology, 52, 67-75. doi:10.1046/j.1365-2265.2000.00873.x
NLM
Marui S, Castro M de, Latronico AC, Elias LLK, Arnhold IJP, Moreira AC, Mendonça BB. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls [Internet]. Clinical Endocrinology. 2000 ; 52 67-75.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.00873.x
Vancouver
Marui S, Castro M de, Latronico AC, Elias LLK, Arnhold IJP, Moreira AC, Mendonça BB. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls [Internet]. Clinical Endocrinology. 2000 ; 52 67-75.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.00873.x
Artigo de periodico
The emergence of salivary cortisol circadin rhythm and its relationship to sleep activity in preterm infants (2000)
Antonini, Sonir Roberto Rauber; Jorge, Salim Moysés; Moreira, Ayrton Custódio
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOLOGIA, PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONINI, Sonir Roberto Rauber e JORGE, Salim Moysés e MOREIRA, Ayrton Custódio. The emergence of salivary cortisol circadin rhythm and its relationship to sleep activity in preterm infants. Clinical Endocrinology, v. 52, p. 423-426, 2000Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2000.tb00561.x. Acesso em: 30 set. 2024.
APA
Antonini, S. R. R., Jorge, S. M., & Moreira, A. C. (2000). The emergence of salivary cortisol circadin rhythm and its relationship to sleep activity in preterm infants. Clinical Endocrinology, 52, 423-426. doi:10.1111/j.1365-2265.2000.tb00561.x
NLM
Antonini SRR, Jorge SM, Moreira AC. The emergence of salivary cortisol circadin rhythm and its relationship to sleep activity in preterm infants [Internet]. Clinical Endocrinology. 2000 ; 52 423-426.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2000.tb00561.x
Vancouver
Antonini SRR, Jorge SM, Moreira AC. The emergence of salivary cortisol circadin rhythm and its relationship to sleep activity in preterm infants [Internet]. Clinical Endocrinology. 2000 ; 52 423-426.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1365-2265.2000.tb00561.x
Artigo de periodico
Salivary cortisol for screening of Cushing's syndrome in children (1999)
Martinelli Júnior, Carlos Eduardo; Sader, Soraya Lopes; Oliveira, Eduardo Brandt de; Daneluzzi, Julio Cesar; Moreira, Ayrton Custódio
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOPATIAS, ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINELLI JÚNIOR, Carlos Eduardo et al. Salivary cortisol for screening of Cushing's syndrome in children. Clinical Endocrinology, v. 51, p. 67-71, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00749.x. Acesso em: 30 set. 2024.
APA
Martinelli Júnior, C. E., Sader, S. L., Oliveira, E. B. de, Daneluzzi, J. C., & Moreira, A. C. (1999). Salivary cortisol for screening of Cushing's syndrome in children. Clinical Endocrinology, 51, 67-71. doi:10.1046/j.1365-2265.1999.00749.x
NLM
Martinelli Júnior CE, Sader SL, Oliveira EB de, Daneluzzi JC, Moreira AC. Salivary cortisol for screening of Cushing's syndrome in children [Internet]. Clinical Endocrinology. 1999 ; 51 67-71.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00749.x
Vancouver
Martinelli Júnior CE, Sader SL, Oliveira EB de, Daneluzzi JC, Moreira AC. Salivary cortisol for screening of Cushing's syndrome in children [Internet]. Clinical Endocrinology. 1999 ; 51 67-71.[citado 2024 set. 30 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00749.x

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