Filtros : "Setian, Nuvarte" "Suiça" Removido: "Grossi, Sonia Aurora Alves" Limpar

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  • Source: Hormone research in paediatrics. Unidade: FM

    Subjects: CRIANÇAS, LEUCEMIA (PATOLOGIA), HORMÔNIOS DA MEDULA ADRENAL (AVALIAÇÃO;ANÁLISE)

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      KUPERMAN, Hilton et al. Evaluation of adrenal reserve in children with acute lymphocytic leukemia treated with prednisone or dexamethasone. Hormone research in paediatrics, v. 78, n. 2, p. 73-78, 2012Tradução . . Disponível em: https://doi.org/10.1159/000339830. Acesso em: 12 set. 2024.
    • APA

      Kuperman, H., Odone Filho, vicente, Cristofani, L. M., Almeida, M. T. A. de, Setian, N., & Damiani, D. (2012). Evaluation of adrenal reserve in children with acute lymphocytic leukemia treated with prednisone or dexamethasone. Hormone research in paediatrics, 78( 2), 73-78. doi:10.1159/000339830
    • NLM

      Kuperman H, Odone Filho vicente, Cristofani LM, Almeida MTA de, Setian N, Damiani D. Evaluation of adrenal reserve in children with acute lymphocytic leukemia treated with prednisone or dexamethasone [Internet]. Hormone research in paediatrics. 2012 ;78( 2): 73-78.[citado 2024 set. 12 ] Available from: https://doi.org/10.1159/000339830
    • Vancouver

      Kuperman H, Odone Filho vicente, Cristofani LM, Almeida MTA de, Setian N, Damiani D. Evaluation of adrenal reserve in children with acute lymphocytic leukemia treated with prednisone or dexamethasone [Internet]. Hormone research in paediatrics. 2012 ;78( 2): 73-78.[citado 2024 set. 12 ] Available from: https://doi.org/10.1159/000339830
  • Source: Clinical Genetics. Unidades: FM, IB

    Subjects: PSICOMOTRICIDADE, MUTAÇÃO GENÉTICA, RETARDO MENTAL

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      VARELA, M. C. et al. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Clinical Genetics, v. 67, n. 1, p. 47-52, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2005.00377.x. Acesso em: 12 set. 2024.
    • APA

      Varela, M. C., Kok, F., Setian, N., Kim, C. A., & Koiffmann, C. P. (2005). Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Clinical Genetics, 67( 1), 47-52. doi:10.1111/j.1399-0004.2005.00377.x
    • NLM

      Varela MC, Kok F, Setian N, Kim CA, Koiffmann CP. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients [Internet]. Clinical Genetics. 2005 ; 67( 1): 47-52.[citado 2024 set. 12 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.x
    • Vancouver

      Varela MC, Kok F, Setian N, Kim CA, Koiffmann CP. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients [Internet]. Clinical Genetics. 2005 ; 67( 1): 47-52.[citado 2024 set. 12 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00377.x

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