Filtros : "HORMÔNIOS" "Clinical Endocrinology" Limpar

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  • Source: Clinical Endocrinology. Unidade: FMRP

    Subjects: GONADOTROFINAS, HORMÔNIOS, PUBERDADE PRECOCE, MENINAS, ESTATURA

    PrivadoAcesso à fonteDOIHow to cite
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    • ABNT

      FRANZINI, Italo Antunes et al. Comments on 'adult height after gonadotropin-releasing hormone agonist treatment in girls with early puberty: a meta-analysis' [Carta]. Clinical Endocrinology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/cen.14292. Acesso em: 27 nov. 2025. , 2020
    • APA

      Franzini, I. A., Yamamoto, F. M., Bolfi, F., Antonini, S. R. R., & Nunes‐Nogueira, V. dos S. (2020). Comments on 'adult height after gonadotropin-releasing hormone agonist treatment in girls with early puberty: a meta-analysis' [Carta]. Clinical Endocrinology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/cen.14292
    • NLM

      Franzini IA, Yamamoto FM, Bolfi F, Antonini SRR, Nunes‐Nogueira V dos S. Comments on 'adult height after gonadotropin-releasing hormone agonist treatment in girls with early puberty: a meta-analysis' [Carta] [Internet]. Clinical Endocrinology. 2020 ; 93( 4): 511-514.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1111/cen.14292
    • Vancouver

      Franzini IA, Yamamoto FM, Bolfi F, Antonini SRR, Nunes‐Nogueira V dos S. Comments on 'adult height after gonadotropin-releasing hormone agonist treatment in girls with early puberty: a meta-analysis' [Carta] [Internet]. Clinical Endocrinology. 2020 ; 93( 4): 511-514.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1111/cen.14292
  • Source: Clinical Endocrinology. Unidade: FM

    Subjects: HORMÔNIOS, PUBERDADE

    Acesso à fonteDOIHow to cite
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    • ABNT

      XAVIER, Ana Claudia Latronico et al. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty. Clinical Endocrinology, v. 59, p. 533-534, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2003.01810.x. Acesso em: 27 nov. 2025.
    • APA

      Xavier, A. C. L., Billerbeck, A. E. C., Pinto, E. M., d'Alva, C. B., Arnhold, I. J. P., & Mendonça, B. B. (2003). Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty. Clinical Endocrinology, 59, 533-534. doi:10.1046/j.1365-2265.2003.01810.x
    • NLM

      Xavier ACL, Billerbeck AEC, Pinto EM, d'Alva CB, Arnhold IJP, Mendonça BB. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty [Internet]. Clinical Endocrinology. 2003 ; 59 533-534.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.x
    • Vancouver

      Xavier ACL, Billerbeck AEC, Pinto EM, d'Alva CB, Arnhold IJP, Mendonça BB. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty [Internet]. Clinical Endocrinology. 2003 ; 59 533-534.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.x
  • Source: Clinical Endocrinology. Unidade: FM

    Subjects: ENDOCRINOLOGIA, HORMÔNIOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      SANTOS, Cecilia L. S. et al. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, v. 51, n. 2, p. 165-172, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00746.x. Acesso em: 27 nov. 2025.
    • APA

      Santos, C. L. S., Bikker, H., Rego, K. G. M., Nascimento, A. C., Tambascia, M., Vijlder, J. J. M. de, & Medeiros Neto, G. A. (1999). A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, 51( 2), 165-172. doi:10.1046/j.1365-2265.1999.00746.x
    • NLM

      Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
    • Vancouver

      Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
  • Source: Clinical Endocrinology. Unidade: FM

    Subjects: ENDOCRINOLOGIA, HORMÔNIOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      ARNHOLD, Ivo J. P. et al. Clinical features of women with resistance to luteinizing hormone. Clinical Endocrinology, v. 51, n. 6, p. 701-707, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00863.x. Acesso em: 27 nov. 2025.
    • APA

      Arnhold, I. J. P., Latrônico, A. C., Batista, M. C., Izzo, C. R., & Mendonça, B. B. de. (1999). Clinical features of women with resistance to luteinizing hormone. Clinical Endocrinology, 51( 6), 701-707. doi:10.1046/j.1365-2265.1999.00863.x
    • NLM

      Arnhold IJP, Latrônico AC, Batista MC, Izzo CR, Mendonça BB de. Clinical features of women with resistance to luteinizing hormone [Internet]. Clinical Endocrinology. 1999 ; 51( 6): 701-707.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00863.x
    • Vancouver

      Arnhold IJP, Latrônico AC, Batista MC, Izzo CR, Mendonça BB de. Clinical features of women with resistance to luteinizing hormone [Internet]. Clinical Endocrinology. 1999 ; 51( 6): 701-707.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00863.x

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