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Artigo de periodico
ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib (2012)
Vivona, Douglas; Bueno, Carolina Tosin; Lima, Luciene Terezinha de; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Luchessi, André Ducati; Zanichelli, Maria Aparecida; Chiattone, Carlos Sérgio; Guerra-Shinohara, Elvira Maria
Source: Blood Cells, Molecules, and Diseases. Unidade: FCF
Subjects: LEUCEMIA MIELOIDE AGUDA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIVONA, Douglas et al. ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. Blood Cells, Molecules, and Diseases, v. 48, n. 2, p. 132-136, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2011.11.001. Acesso em: 12 nov. 2024.
APA
Vivona, D., Bueno, C. T., Lima, L. T. de, Hirata, R. D. C., Hirata, M. H., Luchessi, A. D., et al. (2012). ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. Blood Cells, Molecules, and Diseases, 48( 2), 132-136. doi:10.1016/j.bcmd.2011.11.001
NLM
Vivona D, Bueno CT, Lima LT de, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS, Guerra-Shinohara EM. ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib [Internet]. Blood Cells, Molecules, and Diseases. 2012 ; 48( 2): 132-136.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2011.11.001
Vancouver
Vivona D, Bueno CT, Lima LT de, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS, Guerra-Shinohara EM. ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib [Internet]. Blood Cells, Molecules, and Diseases. 2012 ; 48( 2): 132-136.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2011.11.001
Artigo de periodico
Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients (2011)
Santos, Paulo Caleb Junior de Lima; Cançado, Rodolfo Delfini; Pereira, Alexandre C; Schettert, Isolmar Tadeu; Soares, Renata A. G; Pagliusi, Regina Alexandre; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Teixiera, Ana C; Figueiredo, Maria Stella; Chiattone, Carlos Sérgio; Krieger, José Eduardo; Guerra-Shinohara, Elvira Maria
Source: Blood Cells, Molecules, and Diseases. Unidades: FCF, FM
Subjects: HEMOCROMATOSE, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo Caleb Junior de Lima et al. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients. Blood Cells, Molecules, and Diseases, v. 46, n. 4, p. 302-307, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2011.02.008. Acesso em: 12 nov. 2024.
APA
Santos, P. C. J. de L., Cançado, R. D., Pereira, A. C., Schettert, I. T., Soares, R. A. G., Pagliusi, R. A., et al. (2011). Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients. Blood Cells, Molecules, and Diseases, 46( 4), 302-307. doi:10.1016/j.bcmd.2011.02.008
NLM
Santos PCJ de L, Cançado RD, Pereira AC, Schettert IT, Soares RAG, Pagliusi RA, Hirata RDC, Hirata MH, Teixiera AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients [Internet]. Blood Cells, Molecules, and Diseases. 2011 ; 46( 4): 302-307.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2011.02.008
Vancouver
Santos PCJ de L, Cançado RD, Pereira AC, Schettert IT, Soares RAG, Pagliusi RA, Hirata RDC, Hirata MH, Teixiera AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients [Internet]. Blood Cells, Molecules, and Diseases. 2011 ; 46( 4): 302-307.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2011.02.008
Artigo de periodico
HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing (2010)
Santos, Paulo Caleb Junior de Lima; Pereira, Alexandre C; Cançado, Rodolfo Delfini; Schttert, Isolmar T; Sobreira, Tiago J. Paschoal; Oliveira, Paulo S. L; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Figueiredo, Maria Stella; Chiattone, Carlos Sérgio; Krieger, José Eduardo; Guerra-Shinohara, Elvira Maria
Source: Blood Cells, Molecules, and Diseases. Unidades: FCF, FM
Subjects: MUTAÇÃO GENÉTICA, HEMOCROMATOSE, MODELAGEM MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo Caleb Junior de Lima et al. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing. Blood Cells, Molecules, and Diseases, v. 45, n. 4, p. 302-307, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2010.08.008. Acesso em: 12 nov. 2024.
APA
Santos, P. C. J. de L., Pereira, A. C., Cançado, R. D., Schttert, I. T., Sobreira, T. J. P., Oliveira, P. S. L., et al. (2010). HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing. Blood Cells, Molecules, and Diseases, 45( 4), 302-307. doi:10.1016/j.bcmd.2010.08.008
NLM
Santos PCJ de L, Pereira AC, Cançado RD, Schttert IT, Sobreira TJP, Oliveira PSL, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing [Internet]. Blood Cells, Molecules, and Diseases. 2010 ; 45( 4): 302-307.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2010.08.008
Vancouver
Santos PCJ de L, Pereira AC, Cançado RD, Schttert IT, Sobreira TJP, Oliveira PSL, Hirata RDC, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing [Internet]. Blood Cells, Molecules, and Diseases. 2010 ; 45( 4): 302-307.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.bcmd.2010.08.008

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