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Artigo de periodico
Effects of continuous and intermittent aerobic physical training on hormonal and metabolic profile, and body composition in women with polycystic ovary syndrome: a randomized controlled trial (2020)
Ribeiro, Victor B.; Kogure, Gislaine Satyko ; Lopes, Iris Palma; Silva, Rafael C.; Pedroso, Daiana Cristina Chielli; Melo, Anderson Sanches de ; Souza, Hugo Celso Dutra de ; Ferriani, Rui Alberto ; Furtado, Cristiana Libardi Miranda ; Reis, Rosana Maria dos
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ANTROPOMETRIA, COMPOSIÇÃO CORPORAL, GORDURAS, EXERCÍCIO FÍSICO, HORMÔNIOS SEXUAIS
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ABNT
RIBEIRO, Victor B. et al. Effects of continuous and intermittent aerobic physical training on hormonal and metabolic profile, and body composition in women with polycystic ovary syndrome: a randomized controlled trial. Clinical Endocrinology, v. 93, n. 2, p. 173-186, 2020Tradução . . Disponível em: https://doi.org/10.1111/cen.14194. Acesso em: 16 nov. 2024.
APA
Ribeiro, V. B., Kogure, G. S., Lopes, I. P., Silva, R. C., Pedroso, D. C. C., Melo, A. S. de, et al. (2020). Effects of continuous and intermittent aerobic physical training on hormonal and metabolic profile, and body composition in women with polycystic ovary syndrome: a randomized controlled trial. Clinical Endocrinology, 93( 2), 173-186. doi:10.1111/cen.14194
NLM
Ribeiro VB, Kogure GS, Lopes IP, Silva RC, Pedroso DCC, Melo AS de, Souza HCD de, Ferriani RA, Furtado CLM, Reis RM dos. Effects of continuous and intermittent aerobic physical training on hormonal and metabolic profile, and body composition in women with polycystic ovary syndrome: a randomized controlled trial [Internet]. Clinical Endocrinology. 2020 ; 93( 2): 173-186.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cen.14194
Vancouver
Ribeiro VB, Kogure GS, Lopes IP, Silva RC, Pedroso DCC, Melo AS de, Souza HCD de, Ferriani RA, Furtado CLM, Reis RM dos. Effects of continuous and intermittent aerobic physical training on hormonal and metabolic profile, and body composition in women with polycystic ovary syndrome: a randomized controlled trial [Internet]. Clinical Endocrinology. 2020 ; 93( 2): 173-186.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/cen.14194
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
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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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2011.04054.x
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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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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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2010.03871.x
Artigo de periodico
Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians (2009)
Vendramini, Marcio F.; Kasamatsu, Teresa S.; Crispim, Felipe; Ferreira, Sandra Roberta Gouvea; Matioli, Sergio Russo ; Moisés, Regina S.
Source: Clinical Endocrinology. Unidades: IB, FSP
Assunto: DIABETES MELLITUS
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ABNT
VENDRAMINI, Marcio F. et al. Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians. Clinical Endocrinology, v. 71, n. 1, p. 50-55, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2008.03439.x. Acesso em: 16 nov. 2024.
APA
Vendramini, M. F., Kasamatsu, T. S., Crispim, F., Ferreira, S. R. G., Matioli, S. R., & Moisés, R. S. (2009). Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians. Clinical Endocrinology, 71( 1), 50-55. doi:10.1111/j.1365-2265.2008.03439.x
NLM
Vendramini MF, Kasamatsu TS, Crispim F, Ferreira SRG, Matioli SR, Moisés RS. Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians [Internet]. Clinical Endocrinology. 2009 ; 71( 1): 50-55.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2008.03439.x
Vancouver
Vendramini MF, Kasamatsu TS, Crispim F, Ferreira SRG, Matioli SR, Moisés RS. Novel mutation in the adiponectin (ADIPOQ) gene is associated with hypoadiponectinaemia in Japanese-Brazilians [Internet]. Clinical Endocrinology. 2009 ; 71( 1): 50-55.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2008.03439.x
Artigo de periodico
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene (2008)
Rocha, Rosana O.; Billerbeck, Ana Elisa C.; Pinto, Emília M.; Melo, Karla F. S.; Lin, Chin J.; Longui, Carlos A.; Mendonca, Berenice B.; Bachega, Tânia A. S. S.
Source: Clinical Endocrinology. Unidade: FM
Subjects: GENITÁLIA FEMININA, ADOLESCENTES, FENÓTIPOS, HIDROXILASE (DEFICIÊNCIA), RECEPTORES ANDROGÊNICOS, CONFERÊNCIA INTERNACIONAL
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ABNT
ROCHA, Rosana O. et al. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene. Clinical Endocrinology, v. 68, n. 2, p. 226-232, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.03023.x. Acesso em: 16 nov. 2024.
APA
Rocha, R. O., Billerbeck, A. E. C., Pinto, E. M., Melo, K. F. S., Lin, C. J., Longui, C. A., et al. (2008). The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene. Clinical Endocrinology, 68( 2), 226-232. doi:10.1111/j.1365-2265.2007.03023.x
NLM
Rocha RO, Billerbeck AEC, Pinto EM, Melo KFS, Lin CJ, Longui CA, Mendonca BB, Bachega TASS. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene [Internet]. Clinical Endocrinology. 2008 ; 68( 2): 226-232.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03023.x
Vancouver
Rocha RO, Billerbeck AEC, Pinto EM, Melo KFS, Lin CJ, Longui CA, Mendonca BB, Bachega TASS. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene [Internet]. Clinical Endocrinology. 2008 ; 68( 2): 226-232.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03023.x
Artigo de periodico
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients (2008)
Ferreira, Lize V.; Souza, Silvia C. A. L.; Montenegro, Luciana R.; Malaquias, Alexsandra C.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Jorge, Alexander A. L.
Source: Clinical Endocrinology. Unidade: FM
Subjects: GENES, FATORES DE CRESCIMENTO (GENÉTICA), NANISMO (GENÉTICA), CRINAÇAS
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ABNT
FERREIRA, Lize V. et al. Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients. Clinical Endocrinology, v. 69, n. 3, p. 426-431, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2008.03234.x. Acesso em: 16 nov. 2024.
APA
Ferreira, L. V., Souza, S. C. A. L., Montenegro, L. R., Malaquias, A. C., Arnhold, I. J. P., Mendonca, B. B., & Jorge, A. A. L. (2008). Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients. Clinical Endocrinology, 69( 3), 426-431. doi:10.1111/j.1365-2265.2008.03234.x
NLM
Ferreira LV, Souza SCAL, Montenegro LR, Malaquias AC, Arnhold IJP, Mendonca BB, Jorge AAL. Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients [Internet]. Clinical Endocrinology. 2008 ; 69( 3): 426-431.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2008.03234.x
Vancouver
Ferreira LV, Souza SCAL, Montenegro LR, Malaquias AC, Arnhold IJP, Mendonca BB, Jorge AAL. Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients [Internet]. Clinical Endocrinology. 2008 ; 69( 3): 426-431.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2008.03234.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
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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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03160.x
Artigo de periodico
Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing’s disease (2008)
Romanholi, Daniella Jesus Patrick Carminatti; Machado, Marcio Carlos; Pereira, Camila Canteiro; Danilovic, Debora Seguro; Pereira, Maria Adelaide Albergaria; Cescato, Valter Angelo S.; Cunha Neto, Malebranche Berardo C.; Musolino, Nina Rosa Castro; Mendonça, Berenice Bilharinho de; Salgado, Luiz Roberto
Source: Clinical Endocrinology. Unidades: FM, HU
Subjects: PERÍODO PÓS-OPERATÓRIO, FATORES DE RISCO, GLÂNDULA PRITUITÁRIA (FISIOPATOLOGIA;SECREÇÃO), RECIDIVA, SEGUIMENTOS
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ABNT
ROMANHOLI, Daniella Jesus Patrick Carminatti et al. Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing’s disease. Clinical Endocrinology, v. 69, n. 1, p. 117-122, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.03168.x. Acesso em: 16 nov. 2024.
APA
Romanholi, D. J. P. C., Machado, M. C., Pereira, C. C., Danilovic, D. S., Pereira, M. A. A., Cescato, V. A. S., et al. (2008). Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing’s disease. Clinical Endocrinology, 69( 1), 117-122. doi:10.1111/j.1365-2265.2007.03168.x
NLM
Romanholi DJPC, Machado MC, Pereira CC, Danilovic DS, Pereira MAA, Cescato VAS, Cunha Neto MBC, Musolino NRC, Mendonça BB de, Salgado LR. Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing’s disease [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 117-122.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03168.x
Vancouver
Romanholi DJPC, Machado MC, Pereira CC, Danilovic DS, Pereira MAA, Cescato VAS, Cunha Neto MBC, Musolino NRC, Mendonça BB de, Salgado LR. Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing’s disease [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 117-122.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03168.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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02698.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
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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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02706.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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02765.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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02702.x
Artigo de periodico
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion (2006)
Abrão, Milena Garcia; Leitet, M. V.; Carvalho, L. R.; Billerbeck, A. E. C.; Nishi, M. Y.; Barbosa, A. S.; Martin, R. M.; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS HIPOFISÁRIOS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABRÃO, Milena Garcia et al. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, v. 65, n. 3, p. 294-300, 2006Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02592.x. Acesso em: 16 nov. 2024.
APA
Abrão, M. G., Leitet, M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., et al. (2006). Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, 65( 3), 294-300. doi:10.1111/j.1365-2265.2006.02592.x
NLM
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.x
Vancouver
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.02103.x

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