Filtros : "ENDOCRINOLOGIA" "European Journal of Endocrinology" "FM" Removidos: "IFSC333" "Indexado na Base de dados Science Citation Index" "Suécia" Limpar

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  • Fonte: European Journal of Endocrinology. Unidade: FM

    Assuntos: CLÍNICA GERAL, ENDOCRINOLOGIA

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    • ABNT

      TREVINO, O. Gonzalez et al. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. Reino Unido: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 31 out. 2024. , 2001
    • APA

      Trevino, O. G., Arseven Karamanoglu, O., Ceballos, C. J., Vives, V. I., Ramirez, R. C., Gomez, V. V., et al. (2001). Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. Reino Unido: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Trevino OG, Arseven Karamanoglu O, Ceballos CJ, Vives VI, Ramirez RC, Gomez VV, Medeiros-Neto G, Kopp P. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. 2001 ; 144( 6): 585-593.[citado 2024 out. 31 ]
    • Vancouver

      Trevino OG, Arseven Karamanoglu O, Ceballos CJ, Vives VI, Ramirez RC, Gomez VV, Medeiros-Neto G, Kopp P. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. 2001 ; 144( 6): 585-593.[citado 2024 out. 31 ]
  • Fonte: European Journal of Endocrinology. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      HAYASHIDA, Cesar Yoiti et al. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, v. 142, n. 06, p. 557-563, 2000Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1420557. Acesso em: 31 out. 2024.
    • APA

      Hayashida, C. Y., Gondo, R. G., Ferrari, C., Toledo, S. P. A., Salvatori, R., Levine, M. A., et al. (2000). Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, 142( 06), 557-563. doi:10.1530/eje.0.1420557
    • NLM

      Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1420557
    • Vancouver

      Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1420557
  • Fonte: European Journal of Endocrinology. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      TOLEDO, S. P. A. Inactivating mutations of the LH receptor gene: more than two different phenotypes. European Journal of Endocrinology, v. 140, n. 2, p. 186, 1999Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1400186. Acesso em: 31 out. 2024.
    • APA

      Toledo, S. P. A. (1999). Inactivating mutations of the LH receptor gene: more than two different phenotypes. European Journal of Endocrinology, 140( 2), 186. doi:10.1530/eje.0.1400186
    • NLM

      Toledo SPA. Inactivating mutations of the LH receptor gene: more than two different phenotypes [Internet]. European Journal of Endocrinology. 1999 ; 140( 2): 186.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1400186
    • Vancouver

      Toledo SPA. Inactivating mutations of the LH receptor gene: more than two different phenotypes [Internet]. European Journal of Endocrinology. 1999 ; 140( 2): 186.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1400186
  • Fonte: European Journal of Endocrinology. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      DAMIANI, Durval et al. True hermaphroditism: clinical aspects and molecular studies in 16 cases. European Journal of Endocrinology, v. 136, n. 2, p. 201-204, 1997Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1360201. Acesso em: 31 out. 2024.
    • APA

      Damiani, D., Fellous, M., McElreavey, K., Barbaux, S., Barreto, E. S. A., Dichtchekenian, V., & Setian, N. (1997). True hermaphroditism: clinical aspects and molecular studies in 16 cases. European Journal of Endocrinology, 136( 2), 201-204. doi:10.1530/eje.0.1360201
    • NLM

      Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ESA, Dichtchekenian V, Setian N. True hermaphroditism: clinical aspects and molecular studies in 16 cases [Internet]. European Journal of Endocrinology. 1997 ; 136( 2): 201-204.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1360201
    • Vancouver

      Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ESA, Dichtchekenian V, Setian N. True hermaphroditism: clinical aspects and molecular studies in 16 cases [Internet]. European Journal of Endocrinology. 1997 ; 136( 2): 201-204.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1360201
  • Fonte: European Journal of Endocrinology. Nome do evento: European Congress of Endocrinology. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      BORGES, M F et al. Calcitonin (ct) deficiency in chronic hashimoto's thyroiditis. European Journal of Endocrinology. Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 31 out. 2024. , 1994
    • APA

      Borges, M. F., Toledo, S. P. A., Abelin, N. M. A., Cunha, D. F., & Barros, M. A. E. (1994). Calcitonin (ct) deficiency in chronic hashimoto's thyroiditis. European Journal of Endocrinology. Oxford: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Borges MF, Toledo SPA, Abelin NMA, Cunha DF, Barros MAE. Calcitonin (ct) deficiency in chronic hashimoto's thyroiditis. European Journal of Endocrinology. 1994 ;130( ju 1994): 140.[citado 2024 out. 31 ]
    • Vancouver

      Borges MF, Toledo SPA, Abelin NMA, Cunha DF, Barros MAE. Calcitonin (ct) deficiency in chronic hashimoto's thyroiditis. European Journal of Endocrinology. 1994 ;130( ju 1994): 140.[citado 2024 out. 31 ]
  • Fonte: European Journal of Endocrinology. Nome do evento: Annual Meeting of the American Thyroid Association. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      GAITAN, E et al. Antythyroid effects in vivo and in vitro of babassu and mandioca: a staple food in goiter areas of brazil. European Journal of Endocrinology. Oslo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 31 out. 2024. , 1994
    • APA

      Gaitan, E., Cooksey, R. C., Legan, J., Lindsay, R., Ingbar, S., & Medeiros Neto, G. A. (1994). Antythyroid effects in vivo and in vitro of babassu and mandioca: a staple food in goiter areas of brazil. European Journal of Endocrinology. Oslo: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Gaitan E, Cooksey RC, Legan J, Lindsay R, Ingbar S, Medeiros Neto GA. Antythyroid effects in vivo and in vitro of babassu and mandioca: a staple food in goiter areas of brazil. European Journal of Endocrinology. 1994 ;131( 2 ): 138-44.[citado 2024 out. 31 ]
    • Vancouver

      Gaitan E, Cooksey RC, Legan J, Lindsay R, Ingbar S, Medeiros Neto GA. Antythyroid effects in vivo and in vitro of babassu and mandioca: a staple food in goiter areas of brazil. European Journal of Endocrinology. 1994 ;131( 2 ): 138-44.[citado 2024 out. 31 ]
  • Fonte: European Journal of Endocrinology. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      DAHIA, P L M et al. Low cor blood levels of catecholamine from a newborn of a pheochromocytoma patient. European Journal of Endocrinology, v. 130, n. 3 , p. 217-9, 1994Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1300217. Acesso em: 31 out. 2024.
    • APA

      Dahia, P. L. M., Hayashida, C. Y., Strunz, C. M. C., Abelin, N. M. A., & Toledo, S. P. A. (1994). Low cor blood levels of catecholamine from a newborn of a pheochromocytoma patient. European Journal of Endocrinology, 130( 3 ), 217-9. doi:10.1530/eje.0.1300217
    • NLM

      Dahia PLM, Hayashida CY, Strunz CMC, Abelin NMA, Toledo SPA. Low cor blood levels of catecholamine from a newborn of a pheochromocytoma patient [Internet]. European Journal of Endocrinology. 1994 ;130( 3 ): 217-9.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1300217
    • Vancouver

      Dahia PLM, Hayashida CY, Strunz CMC, Abelin NMA, Toledo SPA. Low cor blood levels of catecholamine from a newborn of a pheochromocytoma patient [Internet]. European Journal of Endocrinology. 1994 ;130( 3 ): 217-9.[citado 2024 out. 31 ] Available from: https://doi.org/10.1530/eje.0.1300217

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