Menu

Filtros : "Lange, A. P." Limpar

Filtros

Refine with date range

  • 1

1 - 2 (2 records)

  • Artigo de periodico-carta/editorial

    The experience of the International Consortium on Acute Promyelocytic Leukemia in monitoring minimal residual disease in acute promyelocytic leukaemia. [Carta] (2018)

    Lange, A. P.; Lima, Ana S.; Lucena-Araújo, Antonio Roberto; Jácomo, Rafael H.; Melo, Raul A.; Bittencourt, Rosane I.; Pasquini, Ricardo; Pagnano, Katia; Fagundes, Evandro M.; Rego, Eduardo Magalhães

    Source: British Journal of Haematology. Unidade: FMRP

    Subjects: LEUCEMIA, PROTEÍNAS PROTO-ONCOGÊNICAS

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

    • ABNT

      LANGE, A. P. et al. The experience of the International Consortium on Acute Promyelocytic Leukemia in monitoring minimal residual disease in acute promyelocytic leukaemia. [Carta]. British Journal of Haematology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/bjh.14490. Acesso em: 30 set. 2024. , 2018

    • APA

      Lange, A. P., Lima, A. S., Lucena-Araújo, A. R., Jácomo, R. H., Melo, R. A., Bittencourt, R. I., et al. (2018). The experience of the International Consortium on Acute Promyelocytic Leukemia in monitoring minimal residual disease in acute promyelocytic leukaemia. [Carta]. British Journal of Haematology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/bjh.14490

    • NLM

      Lange AP, Lima AS, Lucena-Araújo AR, Jácomo RH, Melo RA, Bittencourt RI, Pasquini R, Pagnano K, Fagundes EM, Rego EM. The experience of the International Consortium on Acute Promyelocytic Leukemia in monitoring minimal residual disease in acute promyelocytic leukaemia. [Carta] [Internet]. British Journal of Haematology. 2018 ; 180( 6): 915-918.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/bjh.14490

    • Vancouver

      Lange AP, Lima AS, Lucena-Araújo AR, Jácomo RH, Melo RA, Bittencourt RI, Pasquini R, Pagnano K, Fagundes EM, Rego EM. The experience of the International Consortium on Acute Promyelocytic Leukemia in monitoring minimal residual disease in acute promyelocytic leukaemia. [Carta] [Internet]. British Journal of Haematology. 2018 ; 180( 6): 915-918.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/bjh.14490

  • Artigo de periodico

    A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family (2011)

    Ferraro, M. F.; Moreno, A. S.; Castelli, E. C.; Donadi, Eduardo Antônio; Palma, M. S.; Arcuri, H. A.; Lange, A. P.; Bork, K.; Sarti, Willy; Arruda, Luisa Karla de Paula

    Source: Allergy. Unidade: FMRP

    Subjects: ANGIOEDEMA, DOENÇAS HEREDITÁRIAS, BRADICININA

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

    • ABNT

      FERRARO, M. F. et al. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Allergy, v. 66, n. 10, p. 1384-1390, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1398-9995.2011.02658.x. Acesso em: 30 set. 2024.

    • APA

      Ferraro, M. F., Moreno, A. S., Castelli, E. C., Donadi, E. A., Palma, M. S., Arcuri, H. A., et al. (2011). A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family. Allergy, 66( 10), 1384-1390. doi:10.1111/j.1398-9995.2011.02658.x

    • NLM

      Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK de P. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family [Internet]. Allergy. 2011 ; 66( 10): 1384-1390.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1398-9995.2011.02658.x

    • Vancouver

      Ferraro MF, Moreno AS, Castelli EC, Donadi EA, Palma MS, Arcuri HA, Lange AP, Bork K, Sarti W, Arruda LK de P. A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family [Internet]. Allergy. 2011 ; 66( 10): 1384-1390.[citado 2024 set. 30 ] Available from: https://doi.org/10.1111/j.1398-9995.2011.02658.x
  • 1

1 - 2 (2 records)

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024