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Artigo de periodico
Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy (2010)
Coutinho, Flavia L.; Lourenço Jr., Delmar M.; Toledo, Rodrigo A.; Montenegro, Fabio L. M.; Correia-Deur, Joya E. M.; Toledo, Sergio P. A.
Source: Clinical Endocrinology. Unidade: FM
Subjects: DENSIDADE ÓSSEA, NEOPLASIA ENDÓCRINA MÚLTIPLA, PARATIREOIDECTOMIA
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ABNT
COUTINHO, Flavia L. et al. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy. Clinical Endocrinology, v. 72, n. 4, p. 462-468, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2009.03672.x. Acesso em: 06 jun. 2024.
APA
Coutinho, F. L., Lourenço Jr., D. M., Toledo, R. A., Montenegro, F. L. M., Correia-Deur, J. E. M., & Toledo, S. P. A. (2010). Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy. Clinical Endocrinology, 72( 4), 462-468. doi:10.1111/j.1365-2265.2009.03672.x
NLM
Coutinho FL, Lourenço Jr. DM, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy [Internet]. Clinical Endocrinology. 2010 ; 72( 4): 462-468.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03672.x
Vancouver
Coutinho FL, Lourenço Jr. DM, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy [Internet]. Clinical Endocrinology. 2010 ; 72( 4): 462-468.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03672.x
Artigo de periodico
Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency (2010)
Barbosa, Flávia A. Costa; Fernandes, Vânia F. Tonetto; Carvalho, valdemir M.; Nakamura, Odete H.; Moura, Vivian; Vieira, José G. H.; Bachega, Tânia A. S. S.; Kater, Claudio E.
Source: Clinical Endocrinology. Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), HIPERPLASIA SUPRARRENAL CONGÊNITA, SENSIBILIDADE E ESPECIFICIDADE, MENOPAUSA, BIOLOGIA MOLECULAR, GENÓTIPOS
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ABNT
BARBOSA, Flávia A. Costa et al. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency. Clinical Endocrinology, v. 73, n. 6, p. 700-706, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2010.03871.x. Acesso em: 06 jun. 2024.
APA
Barbosa, F. A. C., Fernandes, V. F. T., Carvalho, valdemir M., Nakamura, O. H., Moura, V., Vieira, J. G. H., et al. (2010). Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency. Clinical Endocrinology, 73( 6), 700-706. doi:10.1111/j.1365-2265.2010.03871.x
NLM
Barbosa FAC, Fernandes VFT, Carvalho valdemir M, Nakamura OH, Moura V, Vieira JGH, Bachega TASS, Kater CE. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2010 ; 73( 6): 700-706.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2010.03871.x
Vancouver
Barbosa FAC, Fernandes VFT, Carvalho valdemir M, Nakamura OH, Moura V, Vieira JGH, Bachega TASS, Kater CE. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2010 ; 73( 6): 700-706.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2010.03871.x
Artigo de periodico
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe (2007)
Melo, Maria Edna; Marui, Suemi; Carvalho, Luciani Renata; Arnhold, Ivo Jorge; Leite, Claudia da Costa; Mendonça, Berenice Bilharinho; Knoepfelmacher, Mirta
Source: Clinical Endocrinology. Unidade: FM
Subjects: GLÂNDULA PITUITÁRIA (SECREÇÃO), HORMÔNIOS HIPOFISÁRIOS (ANÁLISE), GLÂNDULA PITUITÁRIA (PATOLOGIA)
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ABNT
MELO, Maria Edna et al. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe. Clinical Endocrinology, v. 66, p. 95-102, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02692.x. Acesso em: 06 jun. 2024.
APA
Melo, M. E., Marui, S., Carvalho, L. R., Arnhold, I. J., Leite, C. da C., Mendonça, B. B., & Knoepfelmacher, M. (2007). Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe. Clinical Endocrinology, 66, 95-102. doi:10.1111/j.1365-2265.2006.02692.x
NLM
Melo ME, Marui S, Carvalho LR, Arnhold IJ, Leite C da C, Mendonça BB, Knoepfelmacher M. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe [Internet]. Clinical Endocrinology. 2007 ; 66 95-102.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02692.x
Vancouver
Melo ME, Marui S, Carvalho LR, Arnhold IJ, Leite C da C, Mendonça BB, Knoepfelmacher M. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe [Internet]. Clinical Endocrinology. 2007 ; 66 95-102.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02692.x
Artigo de periodico
Shox mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: Frequency and phenotypic variability (2007)
Jorge, Alexander A. L.; Souza, Silvia C.; Nishi, Miriam Y.; Billerbeck, Ana E.; Libório, Débora C. C.; Kim, Chong A.; Arnhold, Ivo J. P.; Mendonça, Berenice Bilharinho
Source: Clinical Endocrinology. Unidade: FM
Subjects: CRESCIMENTO, FEN'PTIPOS, MUTAÇÃO GENÉTICA, RAQUITISMO
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ABNT
JORGE, Alexander A. L. et al. Shox mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: Frequency and phenotypic variability. Clinical Endocrinology, v. 66, p. 130-135, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02698.x. Acesso em: 06 jun. 2024.
APA
Jorge, A. A. L., Souza, S. C., Nishi, M. Y., Billerbeck, A. E., Libório, D. C. C., Kim, C. A., et al. (2007). Shox mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: Frequency and phenotypic variability. Clinical Endocrinology, 66, 130-135. doi:10.1111/j.1365-2265.2006.02698.x
NLM
Jorge AAL, Souza SC, Nishi MY, Billerbeck AE, Libório DCC, Kim CA, Arnhold IJP, Mendonça BB. Shox mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: Frequency and phenotypic variability [Internet]. Clinical Endocrinology. 2007 ; 66 130-135.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02698.x
Vancouver
Jorge AAL, Souza SC, Nishi MY, Billerbeck AE, Libório DCC, Kim CA, Arnhold IJP, Mendonça BB. Shox mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: Frequency and phenotypic variability [Internet]. Clinical Endocrinology. 2007 ; 66 130-135.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02698.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
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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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02956.x
Artigo de periodico
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1 (2007)
Toledo, Rodrigo A.; Lourenço Junior, Delmar M.; Coutinho, Flavia L.; Quedas, Elisangela; Mackowiack, Ivone; Machado, Marcel Cerqueira César; Montenegro, Fabio; Cunha-Neto, Malebranche B. C.; Liberman, Bernardo; Pereira, Maria A. A.; Correa, Pedro H. S.; Toledo, S. P. A.
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOPATIAS (PATOLOGIA;GENÉTICA), NEOPLASIAS (PATOLOGIA;GENÉTGICA), GLÂNDULAS ENDÓCRINAS (PATOLOGIA), MUTAÇÃO GENÉTICA
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ABNT
TOLEDO, Rodrigo A. et al. Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1. Clinical Endocrinology, v. 67, p. 377-384, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.02895.x. Acesso em: 06 jun. 2024.
APA
Toledo, R. A., Lourenço Junior, D. M., Coutinho, F. L., Quedas, E., Mackowiack, I., Machado, M. C. C., et al. (2007). Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1. Clinical Endocrinology, 67, 377-384. doi:10.1111/j.1365-2265.2007.02895.x
NLM
Toledo RA, Lourenço Junior DM, Coutinho FL, Quedas E, Mackowiack I, Machado MCC, Montenegro F, Cunha-Neto MBC, Liberman B, Pereira MAA, Correa PHS, Toledo SPA. Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1 [Internet]. Clinical Endocrinology. 2007 ; 67 377-384.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02895.x
Vancouver
Toledo RA, Lourenço Junior DM, Coutinho FL, Quedas E, Mackowiack I, Machado MCC, Montenegro F, Cunha-Neto MBC, Liberman B, Pereira MAA, Correa PHS, Toledo SPA. Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1 [Internet]. Clinical Endocrinology. 2007 ; 67 377-384.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02895.x
Artigo de periodico
Impairment of bone mass development in children with chronic cholestatic liver disease (2007)
Taveira, Adriana Távora de Albuquerque; Fernandes, Maria Inez Machado; Galvão, Lívia Carvalho; Sawamura, Regina; Vieira, Enaldo de Mello; Paula, Francisco José Albuquerque de
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: OSTEOPATIAS METABÓLICAS, COLELITÍASE, PEDIATRIA
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ABNT
TAVEIRA, Adriana Távora de Albuquerque et al. Impairment of bone mass development in children with chronic cholestatic liver disease. Clinical Endocrinology, v. 66, p. 518-523, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.02765.x. Acesso em: 06 jun. 2024.
APA
Taveira, A. T. de A., Fernandes, M. I. M., Galvão, L. C., Sawamura, R., Vieira, E. de M., & Paula, F. J. A. de. (2007). Impairment of bone mass development in children with chronic cholestatic liver disease. Clinical Endocrinology, 66, 518-523. doi:10.1111/j.1365-2265.2007.02765.x
NLM
Taveira AT de A, Fernandes MIM, Galvão LC, Sawamura R, Vieira E de M, Paula FJA de. Impairment of bone mass development in children with chronic cholestatic liver disease [Internet]. Clinical Endocrinology. 2007 ; 66 518-523.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02765.x
Vancouver
Taveira AT de A, Fernandes MIM, Galvão LC, Sawamura R, Vieira E de M, Paula FJA de. Impairment of bone mass development in children with chronic cholestatic liver disease [Internet]. Clinical Endocrinology. 2007 ; 66 518-523.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02765.x
Artigo de periodico
Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation (2005)
Araujo, Rogério S.; Billerbeck, Ana Elisa C.; Madureira, Guiomar; Mendonça, Berenice Bilharinho; Bachega, Tânia A. S. S.
Source: Clinical Endocrinology. Unidade: FM
Subjects: FENÓTIPOS, HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (ATIVIDADE)
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ABNT
ARAUJO, Rogério S. et al. Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation. Clinical Endocrinology, v. 62, p. 132-136, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2005.02184.x. Acesso em: 06 jun. 2024.
APA
Araujo, R. S., Billerbeck, A. E. C., Madureira, G., Mendonça, B. B., & Bachega, T. A. S. S. (2005). Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation. Clinical Endocrinology, 62, 132-136. doi:10.1111/j.1365-2265.2005.02184.x
NLM
Araujo RS, Billerbeck AEC, Madureira G, Mendonça BB, Bachega TASS. Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation [Internet]. Clinical Endocrinology. 2005 ; 62 132-136.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2005.02184.x
Vancouver
Araujo RS, Billerbeck AEC, Madureira G, Mendonça BB, Bachega TASS. Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation [Internet]. Clinical Endocrinology. 2005 ; 62 132-136.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2005.02184.x
Artigo de periodico
Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis (2005)
Oler, Gisele; Ebina, Katia N.; Michaluart Jr, Pedro; Kimura, Edna Teruko ; Cerutti, Janete
Source: Clinical Endocrinology. Unidade: ICB
Assunto: HISTOLOGIA
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ABNT
OLER, Gisele et al. Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis. Clinical Endocrinology, v. 62, p. 509-511, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2005.02235.x. Acesso em: 06 jun. 2024.
APA
Oler, G., Ebina, K. N., Michaluart Jr, P., Kimura, E. T., & Cerutti, J. (2005). Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis. Clinical Endocrinology, 62, 509-511. doi:10.1111/j.1365-2265.2005.02235.x
NLM
Oler G, Ebina KN, Michaluart Jr P, Kimura ET, Cerutti J. Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis [Internet]. Clinical Endocrinology. 2005 ; 62 509-511.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2005.02235.x
Vancouver
Oler G, Ebina KN, Michaluart Jr P, Kimura ET, Cerutti J. Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis [Internet]. Clinical Endocrinology. 2005 ; 62 509-511.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2005.02235.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
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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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02075.x
Artigo de periodico
Metabolism of chylomicrons in patients with congenital lipoatrophic diabetes: a study with emulsion models of chylomicrons (2004)
Wajchenberg, Bernardo Leo; Amâncio, Rosângela Fernandes; Santomauro, Ana Tereza; Maranhão, Raul Cavalcante
Source: Clinical Endocrinology. Unidades: FCF, FM
Subjects: DIABETES MELLITUS, LIPOPROTEÍNAS
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ABNT
WAJCHENBERG, Bernardo Leo et al. Metabolism of chylomicrons in patients with congenital lipoatrophic diabetes: a study with emulsion models of chylomicrons. Clinical Endocrinology, v. 61, n. 3, p. 347-352, 2004Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2004.02103.x. Acesso em: 06 jun. 2024.
APA
Wajchenberg, B. L., Amâncio, R. F., Santomauro, A. T., & Maranhão, R. C. (2004). Metabolism of chylomicrons in patients with congenital lipoatrophic diabetes: a study with emulsion models of chylomicrons. Clinical Endocrinology, 61( 3), 347-352. doi:10.1111/j.1365-2265.2004.02103.x
NLM
Wajchenberg BL, Amâncio RF, Santomauro AT, Maranhão RC. Metabolism of chylomicrons in patients with congenital lipoatrophic diabetes: a study with emulsion models of chylomicrons [Internet]. Clinical Endocrinology. 2004 ; 61( 3): 347-352.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02103.x
Vancouver
Wajchenberg BL, Amâncio RF, Santomauro AT, Maranhão RC. Metabolism of chylomicrons in patients with congenital lipoatrophic diabetes: a study with emulsion models of chylomicrons [Internet]. Clinical Endocrinology. 2004 ; 61( 3): 347-352.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02103.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: 06 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. 06 ] 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. 06 ] 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
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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: 06 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. 06 ] 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. 06 ] 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: 06 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. 06 ] 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. 06 ] 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: 06 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. 06 ] 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. 06 ] 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: 06 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. 06 ] 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. 06 ] 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: 06 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. 06 ] 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. 06 ] 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: 06 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. 06 ] 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. 06 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00749.x

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