ReP USP - Resultado da busca

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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] Available from: https://doi.org/10.1111/cen.13984
Artigo de periodico
HLA-G 3' untranslated region polymorphic sites associated with increased HLA-G production are more frequent in patients exhibiting differentiated thyroid tumours (2017)
Figueiredo-Feitosa, Nathalie Lobo de; Palomino, Gustavo Martelli; Alves, Daiani Cristina Cilião; Mendes Júnior, Celso Teixeira; Donadi, Eduardo Antônio; Maciel, Léa Maria Zanini
Source: Clinical Endocrinology. Unidades: FFCLRP, FMRP
Subjects: ANTÍGENOS HLA, POLIMORFISMO, EXPRESSÃO GÊNICA, GLÂNDULA TIREOIDE, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIGUEIREDO-FEITOSA, Nathalie Lobo de et al. HLA-G 3' untranslated region polymorphic sites associated with increased HLA-G production are more frequent in patients exhibiting differentiated thyroid tumours. Clinical Endocrinology, v. 86, n. 4, p. 597-605, 2017Tradução . . Disponível em: https://doi.org/10.1111/cen.13289. Acesso em: 04 jun. 2024.
APA
Figueiredo-Feitosa, N. L. de, Palomino, G. M., Alves, D. C. C., Mendes Júnior, C. T., Donadi, E. A., & Maciel, L. M. Z. (2017). HLA-G 3' untranslated region polymorphic sites associated with increased HLA-G production are more frequent in patients exhibiting differentiated thyroid tumours. Clinical Endocrinology, 86( 4), 597-605. doi:10.1111/cen.13289
NLM
Figueiredo-Feitosa NL de, Palomino GM, Alves DCC, Mendes Júnior CT, Donadi EA, Maciel LMZ. HLA-G 3' untranslated region polymorphic sites associated with increased HLA-G production are more frequent in patients exhibiting differentiated thyroid tumours [Internet]. Clinical Endocrinology. 2017 ; 86( 4): 597-605.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.13289
Vancouver
Figueiredo-Feitosa NL de, Palomino GM, Alves DCC, Mendes Júnior CT, Donadi EA, Maciel LMZ. HLA-G 3' untranslated region polymorphic sites associated with increased HLA-G production are more frequent in patients exhibiting differentiated thyroid tumours [Internet]. Clinical Endocrinology. 2017 ; 86( 4): 597-605.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.13289
Artigo de periodico
Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects (2015)
Paulo, Sabrina Soares; Fernandes-Rosa, Fábio L.; Turatti, Wendy; Coeli-Lacchini, Fernanda Borchers; Martinelli Junior, Carlos Eduardo; Nakiri, Guilherme S.; Moreira, Ayrton Custódio; Santos, Antônio Carlos dos; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: NEOPLASIAS CRANIANAS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULO, Sabrina Soares et al. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. Clinical Endocrinology, v. 82, n. 4, p. 562-569, 2015Tradução . . Disponível em: https://doi.org/10.1111/cen.12565. Acesso em: 04 jun. 2024.
APA
Paulo, S. S., Fernandes-Rosa, F. L., Turatti, W., Coeli-Lacchini, F. B., Martinelli Junior, C. E., Nakiri, G. S., et al. (2015). Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. Clinical Endocrinology, 82( 4), 562-569. doi:10.1111/cen.12565
NLM
Paulo SS, Fernandes-Rosa FL, Turatti W, Coeli-Lacchini FB, Martinelli Junior CE, Nakiri GS, Moreira AC, Santos AC dos, Castro M de, Antonini SRR. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects [Internet]. Clinical Endocrinology. 2015 ; 82( 4): 562-569.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12565
Vancouver
Paulo SS, Fernandes-Rosa FL, Turatti W, Coeli-Lacchini FB, Martinelli Junior CE, Nakiri GS, Moreira AC, Santos AC dos, Castro M de, Antonini SRR. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects [Internet]. Clinical Endocrinology. 2015 ; 82( 4): 562-569.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12565
Artigo de periodico
Evaluation of adrenal function in critically ill children (2014)
Balbão, Viviane da Mata Pasti; Costa, Marcela M. A.; Castro, Margaret de; Carlotti, Ana Paula de Carvalho Panzeri
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: GLÂNDULAS SUPRARRENAIS, CORTISOL, ENDOCRINOLOGIA PEDIÁTRICA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BALBÃO, Viviane da Mata Pasti et al. Evaluation of adrenal function in critically ill children. Clinical Endocrinology, v. 81, n. 4, p. 559-565, 2014Tradução . . Disponível em: https://doi.org/10.1111/cen.12444. Acesso em: 04 jun. 2024.
APA
Balbão, V. da M. P., Costa, M. M. A., Castro, M. de, & Carlotti, A. P. de C. P. (2014). Evaluation of adrenal function in critically ill children. Clinical Endocrinology, 81( 4), 559-565. doi:10.1111/cen.12444
NLM
Balbão V da MP, Costa MMA, Castro M de, Carlotti AP de CP. Evaluation of adrenal function in critically ill children [Internet]. Clinical Endocrinology. 2014 ; 81( 4): 559-565.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12444
Vancouver
Balbão V da MP, Costa MMA, Castro M de, Carlotti AP de CP. Evaluation of adrenal function in critically ill children [Internet]. Clinical Endocrinology. 2014 ; 81( 4): 559-565.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12444
Artigo de periodico
Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours (2014)
Mermejo, Livia M.; Leal, Leticia F.; Colli, Leandro M.; Fragoso, Maria C. B. V.; Latronico, Ana C.; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto; Tucci Júnior, Silvio; Martinelli Junior, Carlos Eduardo; Yunes, Jose Andres; Mastellaro, Maria José; Seidinger, Ana L.; Brandalise, Silvia R.; Moreira, Ayrton Custódio; Ramalho, Leandra Naíra Zambelli; Antonini, Sonir Roberto Rauber; Castro, Margaret de
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: GENES, NEOPLASIAS, PEDIATRIA, ADULTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MERMEJO, Livia M. et al. Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours. Clinical Endocrinology, v. 81, n. 4, p. 503-510, 2014Tradução . . Disponível em: https://doi.org/10.1111/cen.12462. Acesso em: 04 jun. 2024.
APA
Mermejo, L. M., Leal, L. F., Colli, L. M., Fragoso, M. C. B. V., Latronico, A. C., Tone, L. G., et al. (2014). Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours. Clinical Endocrinology, 81( 4), 503-510. doi:10.1111/cen.12462
NLM
Mermejo LM, Leal LF, Colli LM, Fragoso MCBV, Latronico AC, Tone LG, Scrideli CA, Tucci Júnior S, Martinelli Junior CE, Yunes JA, Mastellaro MJ, Seidinger AL, Brandalise SR, Moreira AC, Ramalho LNZ, Antonini SRR, Castro M de. Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours [Internet]. Clinical Endocrinology. 2014 ; 81( 4): 503-510.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12462
Vancouver
Mermejo LM, Leal LF, Colli LM, Fragoso MCBV, Latronico AC, Tone LG, Scrideli CA, Tucci Júnior S, Martinelli Junior CE, Yunes JA, Mastellaro MJ, Seidinger AL, Brandalise SR, Moreira AC, Ramalho LNZ, Antonini SRR, Castro M de. Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours [Internet]. Clinical Endocrinology. 2014 ; 81( 4): 503-510.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/cen.12462
Artigo de periodico
Postnatal growth and cardiometabolic profile in young adults born large for gestational age (2011)
Espiñeira, Aniette Renom; Rosa, Fabio Luiz Fernandes; Bueno, Ana Carolina; Souza, Roberto Molina de; Moreira, Ayrton Custódio; Castro, Margaret de; Barbieri, Marco Antonio; Bettiol, Heloisa; Antonini, Sonir Rauber
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: PEDIATRIA, ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPIÑEIRA, Aniette Renom et al. Postnatal growth and cardiometabolic profile in young adults born large for gestational age. Clinical Endocrinology, v. 75, n. 3, p. 335-341, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2011.04054.x. Acesso em: 04 jun. 2024.
APA
Espiñeira, A. R., Rosa, F. L. F., Bueno, A. C., Souza, R. M. de, Moreira, A. C., Castro, M. de, et al. (2011). Postnatal growth and cardiometabolic profile in young adults born large for gestational age. Clinical Endocrinology, 75( 3), 335-341. doi:10.1111/j.1365-2265.2011.04054.x
NLM
Espiñeira AR, Rosa FLF, Bueno AC, Souza RM de, Moreira AC, Castro M de, Barbieri MA, Bettiol H, Antonini SR. Postnatal growth and cardiometabolic profile in young adults born large for gestational age [Internet]. Clinical Endocrinology. 2011 ; 75( 3): 335-341.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2011.04054.x
Vancouver
Espiñeira AR, Rosa FLF, Bueno AC, Souza RM de, Moreira AC, Castro M de, Barbieri MA, Bettiol H, Antonini SR. Postnatal growth and cardiometabolic profile in young adults born large for gestational age [Internet]. Clinical Endocrinology. 2011 ; 75( 3): 335-341.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2011.04054.x
Artigo de periodico
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole (2008)
Almeida, Madson Queiroz; Brito, Vinicius Nahime; Lins, Thereza Selma S.; Guerra-Júnior, Gil; Castro, Margaret de; Antonini, Sonir Roberto; Arnhold, Ivo Jorge Prado; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Source: Clinical Endocrinology. Unidades: FM, FMRP
Subjects: ENDOCRINOLOGIA, PUBERDADE PRECOCE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Madson Queiroz et al. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, v. 69, n. 1, p. 93-98, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.03160.x. Acesso em: 04 jun. 2024.
APA
Almeida, M. Q., Brito, V. N., Lins, T. S. S., Guerra-Júnior, G., Castro, M. de, Antonini, S. R., et al. (2008). Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, 69( 1), 93-98. doi:10.1111/j.1365-2265.2007.03160.x
NLM
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 93-98.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03160.x
Vancouver
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 93-98.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03160.x
Artigo de periodico
Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone (2007)
Magalhães, Patrícia Künzle Ribeiro; Daré, Gustavo Leopoldo Rodrigues; Santos, Sandra Rodrigues dos; Nogueira, Célia Regina; Castro, Margaret de; Maciel, Léa Maria Zanini
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: HORMÔNIOS TIREOIDIANOS, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAGALHÃES, Patrícia Künzle Ribeiro et al. Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone. Clinical Endocrinology, v. 67, p. 748-753, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.02956.x. Acesso em: 04 jun. 2024.
APA
Magalhães, P. K. R., Daré, G. L. R., Santos, S. R. dos, Nogueira, C. R., Castro, M. de, & Maciel, L. M. Z. (2007). Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone. Clinical Endocrinology, 67, 748-753. doi:10.1111/j.1365-2265.2007.02956.x
NLM
Magalhães PKR, Daré GLR, Santos SR dos, Nogueira CR, Castro M de, Maciel LMZ. Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone [Internet]. Clinical Endocrinology. 2007 ; 67 748-753.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02956.x
Vancouver
Magalhães PKR, Daré GLR, Santos SR dos, Nogueira CR, Castro M de, Maciel LMZ. Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone [Internet]. Clinical Endocrinology. 2007 ; 67 748-753.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02956.x
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02706.x
Artigo de periodico
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism (2007)
Versiani, Beatriz R.; Trarbach, Ericka; Koenigkam-Santos, Marcel; Santos, Antonio Carlos dos; Elias, Lucila Leico Kagohara; Moreira, Ayrton Custódio; Latronico, Ana Claudia; Castro, Margaret de
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOLOGIA, HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VERSIANI, Beatriz R. et al. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism. Clinical Endocrinology, v. 66, p. 173-179, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02702.x. Acesso em: 04 jun. 2024.
APA
Versiani, B. R., Trarbach, E., Koenigkam-Santos, M., Santos, A. C. dos, Elias, L. L. K., Moreira, A. C., et al. (2007). Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism. Clinical Endocrinology, 66, 173-179. doi:10.1111/j.1365-2265.2006.02702.x
NLM
Versiani BR, Trarbach E, Koenigkam-Santos M, Santos AC dos, Elias LLK, Moreira AC, Latronico AC, Castro M de. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism [Internet]. Clinical Endocrinology. 2007 ; 66 173-179.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02702.x
Vancouver
Versiani BR, Trarbach E, Koenigkam-Santos M, Santos AC dos, Elias LLK, Moreira AC, Latronico AC, Castro M de. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism [Internet]. Clinical Endocrinology. 2007 ; 66 173-179.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02702.x
Artigo de periodico
Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2004)
Cunha, Heloisa Marcelina; Elias, Lucila Leico Kagohara; Camacho-Hubner, Cecilia; Moreira, Ayrton Custódio; Martinelli Júnior, Carlos Eduardo
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOPATIAS, PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUNHA, Heloisa Marcelina et al. Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinical Endocrinology, v. 61, p. 94-101, 2004Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2004.02075.x. Acesso em: 04 jun. 2024.
APA
Cunha, H. M., Elias, L. L. K., Camacho-Hubner, C., Moreira, A. C., & Martinelli Júnior, C. E. (2004). Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinical Endocrinology, 61, 94-101. doi:10.1111/j.1365-2265.2004.02075.x
NLM
Cunha HM, Elias LLK, Camacho-Hubner C, Moreira AC, Martinelli Júnior CE. Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2004 ; 61 94-101.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02075.x
Vancouver
Cunha HM, Elias LLK, Camacho-Hubner C, Moreira AC, Martinelli Júnior CE. Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2004 ; 61 94-101.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02075.x
Artigo de periodico
A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome (2003)
Castro, Margaret; Elias, Lucila Leico Kagohara; Elias, Paula Conde Lamparelli; Moreira, Ayrton Custódio
Source: Clinical Endocrinology. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Margaret et al. A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome. Clinical Endocrinology, v. 59, p. 800-805, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2003.01908.x. Acesso em: 04 jun. 2024.
APA
Castro, M., Elias, L. L. K., Elias, P. C. L., & Moreira, A. C. (2003). A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome. Clinical Endocrinology, 59, 800-805. doi:10.1046/j.1365-2265.2003.01908.x
NLM
Castro M, Elias LLK, Elias PCL, Moreira AC. A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome [Internet]. Clinical Endocrinology. 2003 ; 59 800-805.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01908.x
Vancouver
Castro M, Elias LLK, Elias PCL, Moreira AC. A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome [Internet]. Clinical Endocrinology. 2003 ; 59 800-805.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01908.x
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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01834.x
Artigo de periodico
Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors (2002)
Antonini, S. R. R.; Latronicot, A. C.; ELIAS, L. L. K.; Cukiert, A. (Hospital Brigadeiro-US, São Paulo, Brasil); Machado, Hélio Rubens; Liberman, Bernardo; Mendonça, Berenice Bilharinho de; Moreira, Ayrton Custódio; Castro, Margaret de
Source: Clinical Endocrinology. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONINI, S. R. R. et al. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors. Clinical Endocrinology, v. 57, p. 657-662, 2002Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2002.01639.x. Acesso em: 04 jun. 2024.
APA
Antonini, S. R. R., Latronicot, A. C., ELIAS, L. L. K., Machado, H. R., Liberman, B., Mendonça, B. B. de, et al. (2002). Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors. Clinical Endocrinology, 57, 657-662. doi:10.1046/j.1365-2265.2002.01639.x
NLM
Antonini SRR, Latronicot AC, ELIAS LLK, Machado HR, Liberman B, Mendonça BB de, Moreira AC, Castro M de. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors [Internet]. Clinical Endocrinology. 2002 ; 57 657-662.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.x
Vancouver
Antonini SRR, Latronicot AC, ELIAS LLK, Machado HR, Liberman B, Mendonça BB de, Moreira AC, Castro M de. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors [Internet]. Clinical Endocrinology. 2002 ; 57 657-662.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] 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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.2000.tb00561.x
Artigo de periodico
Correlation between cortisol and insulin-like growth factor-binding proteins (IGFBPs) under physiological conditions in children (1999)
Martinelli, Carlos Eduardo; Yateman, Martin; Cotterill, Andrews M; Moreira, Ayrton Custódio; Camacho-Hübsner, Cecilia
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, Carlos Eduardo et al. Correlation between cortisol and insulin-like growth factor-binding proteins (IGFBPs) under physiological conditions in children. Clinical Endocrinology, v. 50, p. 767-774, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00724.x. Acesso em: 04 jun. 2024.
APA
Martinelli, C. E., Yateman, M., Cotterill, A. M., Moreira, A. C., & Camacho-Hübsner, C. (1999). Correlation between cortisol and insulin-like growth factor-binding proteins (IGFBPs) under physiological conditions in children. Clinical Endocrinology, 50, 767-774. doi:10.1046/j.1365-2265.1999.00724.x
NLM
Martinelli CE, Yateman M, Cotterill AM, Moreira AC, Camacho-Hübsner C. Correlation between cortisol and insulin-like growth factor-binding proteins (IGFBPs) under physiological conditions in children [Internet]. Clinical Endocrinology. 1999 ; 50 767-774.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00724.x
Vancouver
Martinelli CE, Yateman M, Cotterill AM, Moreira AC, Camacho-Hübsner C. Correlation between cortisol and insulin-like growth factor-binding proteins (IGFBPs) under physiological conditions in children [Internet]. Clinical Endocrinology. 1999 ; 50 767-774.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00724.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: 04 jun. 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 jun. 04 ] 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 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00749.x
Artigo de periodico
Peripheral glucose metabolism in human hiperprolactinemia (1996)
Foss, M C; Paula, F J A; Paccola, G M G F; Piccinato, Carlos Eli
Source: Clinical Endocrinology. Unidade: FMRP
Assunto: ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FOSS, M C et al. Peripheral glucose metabolism in human hiperprolactinemia. Clinical Endocrinology, v. 43, p. 721-6, 1996Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.1995.tb00541.x. Acesso em: 04 jun. 2024.
APA
Foss, M. C., Paula, F. J. A., Paccola, G. M. G. F., & Piccinato, C. E. (1996). Peripheral glucose metabolism in human hiperprolactinemia. Clinical Endocrinology, 43, 721-6. doi:10.1111/j.1365-2265.1995.tb00541.x
NLM
Foss MC, Paula FJA, Paccola GMGF, Piccinato CE. Peripheral glucose metabolism in human hiperprolactinemia [Internet]. Clinical Endocrinology. 1996 ;43 721-6.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.1995.tb00541.x
Vancouver
Foss MC, Paula FJA, Paccola GMGF, Piccinato CE. Peripheral glucose metabolism in human hiperprolactinemia [Internet]. Clinical Endocrinology. 1996 ;43 721-6.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1111/j.1365-2265.1995.tb00541.x
Artigo de periodico
Longitudinal evaluation of development of salivary cortisol circadian rhythm in infancy (1996)
Santiago, L B; Jorge, S M; Moreira, Ayrton Custódio
Source: Clinical Endocrinology. Unidade: FMRP
Assunto: ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTIAGO, L B e JORGE, S M e MOREIRA, Ayrton Custódio. Longitudinal evaluation of development of salivary cortisol circadian rhythm in infancy. Clinical Endocrinology, v. 44, p. 157-161, 1996Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1996.645466.x. Acesso em: 04 jun. 2024.
APA
Santiago, L. B., Jorge, S. M., & Moreira, A. C. (1996). Longitudinal evaluation of development of salivary cortisol circadian rhythm in infancy. Clinical Endocrinology, 44, 157-161. doi:10.1046/j.1365-2265.1996.645466.x
NLM
Santiago LB, Jorge SM, Moreira AC. Longitudinal evaluation of development of salivary cortisol circadian rhythm in infancy [Internet]. Clinical Endocrinology. 1996 ; 44 157-161.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.1996.645466.x
Vancouver
Santiago LB, Jorge SM, Moreira AC. Longitudinal evaluation of development of salivary cortisol circadian rhythm in infancy [Internet]. Clinical Endocrinology. 1996 ; 44 157-161.[citado 2024 jun. 04 ] Available from: https://doi.org/10.1046/j.1365-2265.1996.645466.x

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Indexado em