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Artigo de periodico
Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss (2012)
Guerra-Shinohara, Elvira Maria ; Bertinato, Juliano Felix; Bueno, Carolina Tosin; Silva, Kelma Cordeiro da; Carvalho, Mario Henrique Burlacchini de; Francisco, Rossana Pulcineli Vieira; Zugaib, Marcelo; Cerda, Alvaro; Morelli, Vânia Maris
Source: Thrombosis and Haemostasis. Unidades: FCF, FM
Subjects: POLIMORFISMO, TROMBOEMBOLISMO
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ABNT
GUERRA-SHINOHARA, Elvira Maria et al. Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss. Thrombosis and Haemostasis, v. 108, n. 4, p. 693-700, 2012Tradução . . Disponível em: https://doi.org/10.1160/TH12-03-0177. Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M., Bertinato, J. F., Bueno, C. T., Silva, K. C. da, Carvalho, M. H. B. de, Francisco, R. P. V., et al. (2012). Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss. Thrombosis and Haemostasis, 108( 4), 693-700. doi:10.1160/TH12-03-0177
NLM
Guerra-Shinohara EM, Bertinato JF, Bueno CT, Silva KC da, Carvalho MHB de, Francisco RPV, Zugaib M, Cerda A, Morelli VM. Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss [Internet]. Thrombosis and Haemostasis. 2012 ;108( 4): 693-700.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1160/TH12-03-0177
Vancouver
Guerra-Shinohara EM, Bertinato JF, Bueno CT, Silva KC da, Carvalho MHB de, Francisco RPV, Zugaib M, Cerda A, Morelli VM. Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss [Internet]. Thrombosis and Haemostasis. 2012 ;108( 4): 693-700.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1160/TH12-03-0177
Trabalho de evento-resumo
Polymorphisms in ABC transporter genes are associated with complete molecular response to imatinib in chronic myeloid leukemia patients (2012)
Vivona, Douglas; Lima, Luciene Terezinha de; Bueno, Carolina Tosin; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Luchessi, André Ducati; Zanichelli, Maria Aparecida; Chiattone, Carlos Sérgio; Guerra-Shinohara, Elvira Maria
Source: Abstracts. Conference titles: Congress of the European Hematology Association. Unidade: FCF
Subjects: LEUCEMIA MIELOIDE, POLIMORFISMO
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ABNT
VIVONA, Douglas et al. Polymorphisms in ABC transporter genes are associated with complete molecular response to imatinib in chronic myeloid leukemia patients. 2012, Anais.. The Hague: European Hematology Association, 2012. . Acesso em: 27 abr. 2024.
APA
Vivona, D., Lima, L. T. de, Bueno, C. T., Hirata, R. D. C., Hirata, M. H., Luchessi, A. D., et al. (2012). Polymorphisms in ABC transporter genes are associated with complete molecular response to imatinib in chronic myeloid leukemia patients. In Abstracts. The Hague: European Hematology Association.
NLM
Vivona D, Lima LT de, Bueno CT, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS, Guerra-Shinohara EM. Polymorphisms in ABC transporter genes are associated with complete molecular response to imatinib in chronic myeloid leukemia patients. Abstracts. 2012 ;[citado 2024 abr. 27 ]
Vancouver
Vivona D, Lima LT de, Bueno CT, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS, Guerra-Shinohara EM. Polymorphisms in ABC transporter genes are associated with complete molecular response to imatinib in chronic myeloid leukemia patients. Abstracts. 2012 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Efficacy and safety of deferasirox in patients with iron overload secondary to hereditary hemochromatosis: preliminary results of a 1-YR prospective study (2012)
Cançado, Rodolfo Delfini; Bastos, R; Melo, M; Santos, P; Guerra-Shinohara, Elvira Maria ; Chiattone, Carlos Sérgio
Source: Abstracts. Conference titles: Congress of the European Hematology Association. Unidade: FCF
Subjects: HEMOCROMATOSE, ANEMIA
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ABNT
CANÇADO, Rodolfo Delfini et al. Efficacy and safety of deferasirox in patients with iron overload secondary to hereditary hemochromatosis: preliminary results of a 1-YR prospective study. 2012, Anais.. The Hague: European Hematology Association, 2012. . Acesso em: 27 abr. 2024.
APA
Cançado, R. D., Bastos, R., Melo, M., Santos, P., Guerra-Shinohara, E. M., & Chiattone, C. S. (2012). Efficacy and safety of deferasirox in patients with iron overload secondary to hereditary hemochromatosis: preliminary results of a 1-YR prospective study. In Abstracts. The Hague: European Hematology Association.
NLM
Cançado RD, Bastos R, Melo M, Santos P, Guerra-Shinohara EM, Chiattone CS. Efficacy and safety of deferasirox in patients with iron overload secondary to hereditary hemochromatosis: preliminary results of a 1-YR prospective study. Abstracts. 2012 ;[citado 2024 abr. 27 ]
Vancouver
Cançado RD, Bastos R, Melo M, Santos P, Guerra-Shinohara EM, Chiattone CS. Efficacy and safety of deferasirox in patients with iron overload secondary to hereditary hemochromatosis: preliminary results of a 1-YR prospective study. Abstracts. 2012 ;[citado 2024 abr. 27 ]
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
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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: 27 abr. 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 abr. 27 ] 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 abr. 27 ] Available from: https://doi.org/10.1016/j.bcmd.2011.11.001
Trabalho de evento-resumo periodico
Polypharmacy associated with potentially inapropriate medication in the elderly (2012)
Didone, Thiago Vinicios Nadaleto; Mori, Ana Luiza Pereira Moreira; Dorea, Egidio; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting. Unidade: FCF
Subjects: IDOSOS, MEDICAMENTO
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ABNT
DIDONE, Thiago Vinicios Nadaleto et al. Polypharmacy associated with potentially inapropriate medication in the elderly. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2012
APA
Didone, T. V. N., Mori, A. L. P. M., Dorea, E., & Guerra-Shinohara, E. M. (2012). Polypharmacy associated with potentially inapropriate medication in the elderly. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Didone TVN, Mori ALPM, Dorea E, Guerra-Shinohara EM. Polypharmacy associated with potentially inapropriate medication in the elderly. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 40 res. FCF076.[citado 2024 abr. 27 ]
Vancouver
Didone TVN, Mori ALPM, Dorea E, Guerra-Shinohara EM. Polypharmacy associated with potentially inapropriate medication in the elderly. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 40 res. FCF076.[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter (2012)
Monteiro, Nathalia Sierra; Britto, Jessica Carrilho; Giusti, Kelma Cordeiro da Silva; Carvalho, Mario Henrique Burlacchini de; Amorim Filho, Antonio; Zugaib, Marcelo; Guerra-Shinohara, Elvira Maria
Source: Abstracts. Conference titles: Congress of the International Society of Nutrigenetics/Nutrigenomics. Unidades: FCF, FM
Subjects: ABORTO ESPONTÂNEO, VITAMINAS
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ABNT
MONTEIRO, Nathalia Sierra et al. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. 2012, Anais.. Chieti: International Society of Nutrigenetics/Nutrigenomics (ISNN), 2012. . Acesso em: 27 abr. 2024.
APA
Monteiro, N. S., Britto, J. C., Giusti, K. C. da S., Carvalho, M. H. B. de, Amorim Filho, A., Zugaib, M., & Guerra-Shinohara, E. M. (2012). Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. In Abstracts. Chieti: International Society of Nutrigenetics/Nutrigenomics (ISNN).
NLM
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. Abstracts. 2012 ;[citado 2024 abr. 27 ]
Vancouver
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. Abstracts. 2012 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Interaction between variants of fibrinogen beta chain gene polymorphisms and positive antinuclear antibodies on the risk of having recurrent pregnancy loss (RPL) (2012)
Bertinato, Juliano Felix; Monteiro, Nathalia Sierra; Gomes, Guilherme; Boacnin, Marina do Rosário; Francisco, Rossana Pulcineli Vieira; Amorin Filho, Antônio; Zugaib, Marcelo; Morelli, Vânia Maris; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting. Unidades: FM, FCF
Subjects: POLIMORFISMO, ANTICORPOS, ABORTO ESPONTÂNEO
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ABNT
BERTINATO, Juliano Felix et al. Interaction between variants of fibrinogen beta chain gene polymorphisms and positive antinuclear antibodies on the risk of having recurrent pregnancy loss (RPL). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2012
APA
Bertinato, J. F., Monteiro, N. S., Gomes, G., Boacnin, M. do R., Francisco, R. P. V., Amorin Filho, A., et al. (2012). Interaction between variants of fibrinogen beta chain gene polymorphisms and positive antinuclear antibodies on the risk of having recurrent pregnancy loss (RPL). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bertinato JF, Monteiro NS, Gomes G, Boacnin M do R, Francisco RPV, Amorin Filho A, Zugaib M, Morelli VM, Guerra-Shinohara EM. Interaction between variants of fibrinogen beta chain gene polymorphisms and positive antinuclear antibodies on the risk of having recurrent pregnancy loss (RPL). Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 3 res. FCF002.[citado 2024 abr. 27 ]
Vancouver
Bertinato JF, Monteiro NS, Gomes G, Boacnin M do R, Francisco RPV, Amorin Filho A, Zugaib M, Morelli VM, Guerra-Shinohara EM. Interaction between variants of fibrinogen beta chain gene polymorphisms and positive antinuclear antibodies on the risk of having recurrent pregnancy loss (RPL). Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 3 res. FCF002.[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Effect of acquired and inherent factors associated with thrombosis in women with recurrent pregnancy loss (2012)
Gomes, Guilherme Wataru; Bertinato, Juliano Felix; Monteiro, Nathalia Sierra; Carvalho, Mário Henrique Burlacchini de; Francisco, Rossana Pulcineli Vieira; Zugaib, Marcelo; Morelli, Vânia Maris; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting. Unidades: FM, FCF
Subjects: TROMBOSE, MULHERES, FATORES DE RISCO, GENÓTIPOS, ANTICORPOS, ABORTO ESPONTÂNEO, DOENÇAS PLACENTÁRIAS, RESUMOS (EVENTOS)
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ABNT
GOMES, Guilherme Wataru et al. Effect of acquired and inherent factors associated with thrombosis in women with recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2012
APA
Gomes, G. W., Bertinato, J. F., Monteiro, N. S., Carvalho, M. H. B. de, Francisco, R. P. V., Zugaib, M., et al. (2012). Effect of acquired and inherent factors associated with thrombosis in women with recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gomes GW, Bertinato JF, Monteiro NS, Carvalho MHB de, Francisco RPV, Zugaib M, Morelli VM, Guerra-Shinohara EM. Effect of acquired and inherent factors associated with thrombosis in women with recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 81.[citado 2024 abr. 27 ]
Vancouver
Gomes GW, Bertinato JF, Monteiro NS, Carvalho MHB de, Francisco RPV, Zugaib M, Morelli VM, Guerra-Shinohara EM. Effect of acquired and inherent factors associated with thrombosis in women with recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 81.[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
DNA Methylation rate and vitamins concentrations in women with recurrent miscarriages (2012)
Monteiro, Nathalia Sierra; Britto, Jessica Carrilho; Giusti, Kelma Cordeiro da Silva; Carvalho, Mario Henrique Burlacchini de; Amorim Filho, Antonio; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting. Unidade: FCF
Subjects: ABORTO ESPONTÂNEO, VITAMINAS
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ABNT
MONTEIRO, Nathalia Sierra et al. DNA Methylation rate and vitamins concentrations in women with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2012
APA
Monteiro, N. S., Britto, J. C., Giusti, K. C. da S., Carvalho, M. H. B. de, Amorim Filho, A., & Guerra-Shinohara, E. M. (2012). DNA Methylation rate and vitamins concentrations in women with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Guerra-Shinohara EM. DNA Methylation rate and vitamins concentrations in women with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 13res. FCF022.[citado 2024 abr. 27 ]
Vancouver
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Guerra-Shinohara EM. DNA Methylation rate and vitamins concentrations in women with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 13res. FCF022.[citado 2024 abr. 27 ]
Trabalho de evento-resumo
SLC22A1 polymorphisms are not associated with cytogenetic and molecular response to imatinib mesylate in chronic myelogenous leukemia patients (2011)
Guerra-Shinohara, Elvira Maria ; Bueno, Carolina Tosin; Lima, Luciene Terezinha de; Vivona, Douglas; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Luchessi, André Ducati; Chiattone, Carlos Sérgio; Zanichelli, Maria Aparecida
Source: Abstracts. Conference titles: Annual Congress of the European Hematology Association (EHA). Unidade: FCF
Subjects: POLIMORFISMO, LEUCEMIA MIELOIDE
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ABNT
GUERRA-SHINOHARA, Elvira Maria et al. SLC22A1 polymorphisms are not associated with cytogenetic and molecular response to imatinib mesylate in chronic myelogenous leukemia patients. 2011, Anais.. Hague: European Hematology Association (EHA), 2011. . Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M., Bueno, C. T., Lima, L. T. de, Vivona, D., Hirata, R. D. C., Hirata, M. H., et al. (2011). SLC22A1 polymorphisms are not associated with cytogenetic and molecular response to imatinib mesylate in chronic myelogenous leukemia patients. In Abstracts. Hague: European Hematology Association (EHA).
NLM
Guerra-Shinohara EM, Bueno CT, Lima LT de, Vivona D, Hirata RDC, Hirata MH, Luchessi AD, Chiattone CS, Zanichelli MA. SLC22A1 polymorphisms are not associated with cytogenetic and molecular response to imatinib mesylate in chronic myelogenous leukemia patients. Abstracts. 2011 ;[citado 2024 abr. 27 ]
Vancouver
Guerra-Shinohara EM, Bueno CT, Lima LT de, Vivona D, Hirata RDC, Hirata MH, Luchessi AD, Chiattone CS, Zanichelli MA. SLC22A1 polymorphisms are not associated with cytogenetic and molecular response to imatinib mesylate in chronic myelogenous leukemia patients. Abstracts. 2011 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Haplotype for polymorphisms C1236T, C3435T and C2677T/A in MDR1 gene is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib (2011)
Guerra-Shinohara, Elvira Maria ; 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
Source: Abstracts. Conference titles: Annual Congress of the European Hematology Association (EHA). Unidade: FCF
Subjects: POLIMORFISMO, LEUCEMIA MIELOIDE
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ABNT
GUERRA-SHINOHARA, Elvira Maria et al. Haplotype for polymorphisms C1236T, C3435T and C2677T/A in MDR1 gene is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. 2011, Anais.. Hague: European Hematology Association (EHA), 2011. . Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M., Vivona, D., Bueno, C. T., Lima, L. T. de, Hirata, R. D. C., Hirata, M. H., et al. (2011). Haplotype for polymorphisms C1236T, C3435T and C2677T/A in MDR1 gene is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. In Abstracts. Hague: European Hematology Association (EHA).
NLM
Guerra-Shinohara EM, Vivona D, Bueno CT, Lima LT de, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS. Haplotype for polymorphisms C1236T, C3435T and C2677T/A in MDR1 gene is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. Abstracts. 2011 ;[citado 2024 abr. 27 ]
Vancouver
Guerra-Shinohara EM, Vivona D, Bueno CT, Lima LT de, Hirata RDC, Hirata MH, Luchessi AD, Zanichelli MA, Chiattone CS. Haplotype for polymorphisms C1236T, C3435T and C2677T/A in MDR1 gene is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinib. Abstracts. 2011 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Frequencies of autoantibodies in women with recurrent pregnancy losses (2011)
Monteiro, Nathalia Sierra; Giusti, Kelma Cordeiro da Silva; Carvalho, Mario Henrique Burlacchini de; Amorim Filho, Antônio; Zugaib, Marcelo; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo. Unidades: FM, FCF
Subjects: ANTICORPOS, ABORTO ESPONTÂNEO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTEIRO, Nathalia Sierra et al. Frequencies of autoantibodies in women with recurrent pregnancy losses. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2011
APA
Monteiro, N. S., Giusti, K. C. da S., Carvalho, M. H. B. de, Amorim Filho, A., Zugaib, M., & Guerra-Shinohara, E. M. (2011). Frequencies of autoantibodies in women with recurrent pregnancy losses. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Monteiro NS, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Frequencies of autoantibodies in women with recurrent pregnancy losses. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 5 res. FCF006 .[citado 2024 abr. 27 ]
Vancouver
Monteiro NS, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Frequencies of autoantibodies in women with recurrent pregnancy losses. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 5 res. FCF006 .[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss (2011)
Cavalcante, Silvana Henrique; Lázaro, Robson José; Boacnin, Marina do Rosário; Carvalho, Mario Henrique Burlacchini de; Amorim Filho, Antônio; Zugaib, Marcelo; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo. Unidades: FM, FCF
Subjects: POLIMORFISMO, ABORTO ESPONTÂNEO
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ABNT
CAVALCANTE, Silvana Henrique et al. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2011
APA
Cavalcante, S. H., Lázaro, R. J., Boacnin, M. do R., Carvalho, M. H. B. de, Amorim Filho, A., Zugaib, M., & Guerra-Shinohara, E. M. (2011). The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Cavalcante SH, Lázaro RJ, Boacnin M do R, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 40 res. FCF076.[citado 2024 abr. 27 ]
Vancouver
Cavalcante SH, Lázaro RJ, Boacnin M do R, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 40 res. FCF076.[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages (2011)
Giusti, Kelma Cordeiro da Silva; Carvalho, Mario Henrique Burlacchini de; Amorim Filho, Antônio Gomes; Zugaib, Marcelo; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo. Unidades: FM, FCF
Subjects: ABORTO ESPONTÂNEO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIUSTI, Kelma Cordeiro da Silva et al. Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2011
APA
Giusti, K. C. da S., Carvalho, M. H. B. de, Amorim Filho, A. G., Zugaib, M., & Guerra-Shinohara, E. M. (2011). Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Giusti KC da S, Carvalho MHB de, Amorim Filho AG, Zugaib M, Guerra-Shinohara EM. Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 75 res. FCF145.[citado 2024 abr. 27 ]
Vancouver
Giusti KC da S, Carvalho MHB de, Amorim Filho AG, Zugaib M, Guerra-Shinohara EM. Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 75 res. FCF145.[citado 2024 abr. 27 ]
Trabalho de evento-resumo periodico
Comparação entre as frequências de anemia, deficiências de folato e vitamina B12 em estudos pré e pós-fortificação das farinhas de trigo e milho com ácido fólico e ferro (2011)
Gomes, G. W; Britto, J. C; Seino, Fernanda Midori; Monteiro, N. S; Giusti, Kelma Cordeiro da Silva; Bertinato, Juliano Felix; Lázaro, Robson José; Guerra-Shinohara, Elvira Maria
Source: Revista Brasileira de Hematologia e Hemoterapia. Conference titles: Congresso Brasileiro de Hematologia e Hemoterapia. Unidade: FCF
Subjects: ANEMIA (FREQUÊNCIA), VITAMINA B12 (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, G. W et al. Comparação entre as frequências de anemia, deficiências de folato e vitamina B12 em estudos pré e pós-fortificação das farinhas de trigo e milho com ácido fólico e ferro. Revista Brasileira de Hematologia e Hemoterapia. Rio de Janeiro: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 27 abr. 2024. , 2011
APA
Gomes, G. W., Britto, J. C., Seino, F. M., Monteiro, N. S., Giusti, K. C. da S., Bertinato, J. F., et al. (2011). Comparação entre as frequências de anemia, deficiências de folato e vitamina B12 em estudos pré e pós-fortificação das farinhas de trigo e milho com ácido fólico e ferro. Revista Brasileira de Hematologia e Hemoterapia. Rio de Janeiro: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Gomes GW, Britto JC, Seino FM, Monteiro NS, Giusti KC da S, Bertinato JF, Lázaro RJ, Guerra-Shinohara EM. Comparação entre as frequências de anemia, deficiências de folato e vitamina B12 em estudos pré e pós-fortificação das farinhas de trigo e milho com ácido fólico e ferro. Revista Brasileira de Hematologia e Hemoterapia. 2011 ; 33 53 res. 0111.[citado 2024 abr. 27 ]
Vancouver
Gomes GW, Britto JC, Seino FM, Monteiro NS, Giusti KC da S, Bertinato JF, Lázaro RJ, Guerra-Shinohara EM. Comparação entre as frequências de anemia, deficiências de folato e vitamina B12 em estudos pré e pós-fortificação das farinhas de trigo e milho com ácido fólico e ferro. Revista Brasileira de Hematologia e Hemoterapia. 2011 ; 33 53 res. 0111.[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss (2011)
Guerra-Shinohara, Elvira Maria ; Seino, Fernanda Midori; Bueno, Carolina Tosin; Britto, Jessica Carrilho; Gomes, Guilherme Wataru; Giusti, Kelma Cordeiro da Silva; Bertinato, Juliano Felix; Carvalho, Mário Henrique Bulacchini de; Amorim Filho, Antônio Gomes; D'almeida, Vânia; Zugaib, Marcelo
Source: Abstract Book. Conference titles: International Conference on Homocysteine Metabolism. Unidades: FCF, FM
Subjects: ABORTO ESPONTÂNEO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA-SHINOHARA, Elvira Maria et al. Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss. 2011, Anais.. Lisboa: Escola Superior de Tecnologia da Saúde, 2011. . Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M., Seino, F. M., Bueno, C. T., Britto, J. C., Gomes, G. W., Giusti, K. C. da S., et al. (2011). Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss. In Abstract Book. Lisboa: Escola Superior de Tecnologia da Saúde.
NLM
Guerra-Shinohara EM, Seino FM, Bueno CT, Britto JC, Gomes GW, Giusti KC da S, Bertinato JF, Carvalho MHB de, Amorim Filho AG, D'almeida V, Zugaib M. Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 27 ]
Vancouver
Guerra-Shinohara EM, Seino FM, Bueno CT, Britto JC, Gomes GW, Giusti KC da S, Bertinato JF, Carvalho MHB de, Amorim Filho AG, D'almeida V, Zugaib M. Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss (2011)
Guerra-Shinohara, Elvira Maria ; Lázaro, Robson José; Giusti, Kelma Cordeiro da Silva; Britto, Jessica Carrilho; Cavalcante, Silvana Henrique; Boacnin, Marina do Rosário; Gomes, Guilherme Wataru; Carvalho, Mário Henrique Burlacchini de; Amorim Filho, Antônio Gomes; Zugaib, Marcelo; D'Almeida, Vânia
Source: Abstract Book. Conference titles: International Conference on Homocysteine Metabolism. Unidades: FCF, FM
Subjects: POLIMORFISMO, ABORTO ESPONTÂNEO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA-SHINOHARA, Elvira Maria et al. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. 2011, Anais.. Lisboa: Escola Superior de Tecnologia da Saúde, 2011. . Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M., Lázaro, R. J., Giusti, K. C. da S., Britto, J. C., Cavalcante, S. H., Boacnin, M. do R., et al. (2011). Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. In Abstract Book. Lisboa: Escola Superior de Tecnologia da Saúde.
NLM
Guerra-Shinohara EM, Lázaro RJ, Giusti KC da S, Britto JC, Cavalcante SH, Boacnin M do R, Gomes GW, Carvalho MHB de, Amorim Filho AG, Zugaib M, D'Almeida V. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 27 ]
Vancouver
Guerra-Shinohara EM, Lázaro RJ, Giusti KC da S, Britto JC, Cavalcante SH, Boacnin M do R, Gomes GW, Carvalho MHB de, Amorim Filho AG, Zugaib M, D'Almeida V. Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss. Abstract Book. 2011 ;[citado 2024 abr. 27 ]
Artigo de jornal
Pesquisa relaciona fatores genéticos e nutricionais com o maior risco de ter abortos espontâneos consecutivos (2011)
Guerra-Shinohara, Elvira Maria
Source: FCFnotícias. Unidade: FCF
Subjects: ABORTO ESPONTÂNEO, GENÉTICA, NUTRIÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA-SHINOHARA, Elvira Maria. Pesquisa relaciona fatores genéticos e nutricionais com o maior risco de ter abortos espontâneos consecutivos. Tradução . FCFnotícias, São Paulo, 2011. , n. 16, p. mar. 2011. 2Disponível em: http://www.fcf.usp.br/Noticias/A04N16_0211.pdf. Acesso em: 27 abr. 2024.
APA
Guerra-Shinohara, E. M. (2011). Pesquisa relaciona fatores genéticos e nutricionais com o maior risco de ter abortos espontâneos consecutivos. FCFnotícias, p. mar. 2011. 2. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://www.fcf.usp.br/Noticias/A04N16_0211.pdf
NLM
Guerra-Shinohara EM. Pesquisa relaciona fatores genéticos e nutricionais com o maior risco de ter abortos espontâneos consecutivos [Internet]. FCFnotícias. 2011 ;( 16): mar. 2011. 2.[citado 2024 abr. 27 ] Available from: http://www.fcf.usp.br/Noticias/A04N16_0211.pdf
Vancouver
Guerra-Shinohara EM. Pesquisa relaciona fatores genéticos e nutricionais com o maior risco de ter abortos espontâneos consecutivos [Internet]. FCFnotícias. 2011 ;( 16): mar. 2011. 2.[citado 2024 abr. 27 ] Available from: http://www.fcf.usp.br/Noticias/A04N16_0211.pdf
Artigo de periodico
Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(®) instrument (2011)
Santos, Paulo Caleb Junior de Lima; Soares, Renata Alonso Gadi; Krieger, José Eduardo; Guerra-Shinohara, Elvira Maria ; Pereira, Alexandre Costa
Source: Clinical Chemistry and Laboratory Medicine. Unidades: FM, FCF
Subjects: HEMOCROMATOSE, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo Caleb Junior de Lima et al. Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(®) instrument. Clinical Chemistry and Laboratory Medicine, v. 49, n. 10, p. 1633-1636, 2011Tradução . . Disponível em: https://doi.org/10.1515/cclm.2011.654. Acesso em: 27 abr. 2024.
APA
Santos, P. C. J. de L., Soares, R. A. G., Krieger, J. E., Guerra-Shinohara, E. M., & Pereira, A. C. (2011). Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(®) instrument. Clinical Chemistry and Laboratory Medicine, 49( 10), 1633-1636. doi:10.1515/cclm.2011.654
NLM
Santos PCJ de L, Soares RAG, Krieger JE, Guerra-Shinohara EM, Pereira AC. Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(®) instrument [Internet]. Clinical Chemistry and Laboratory Medicine. 2011 ; 49( 10): 1633-1636.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1515/cclm.2011.654
Vancouver
Santos PCJ de L, Soares RAG, Krieger JE, Guerra-Shinohara EM, Pereira AC. Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(®) instrument [Internet]. Clinical Chemistry and Laboratory Medicine. 2011 ; 49( 10): 1633-1636.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1515/cclm.2011.654
Trabalho de evento-resumo
Frequency of C848T, C859G, C480G and A1222G polymorphisms in SLC22A1 gene in chronic myelogenous leukaemia patients treated with imatinib mesilate (2011)
Bueno, Carolina Tosin; Lima, Luciene Terezinha de; Vivona, Douglas; Guerra-Shinohara, Elvira Maria
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Científica da Universidade de São Paulo (SIICUSP). Unidade: FCF
Subjects: POLIMORFISMO, LEUCEMIA MIELOIDE AGUDA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BUENO, Carolina Tosin et al. Frequency of C848T, C859G, C480G and A1222G polymorphisms in SLC22A1 gene in chronic myelogenous leukaemia patients treated with imatinib mesilate. 2011, Anais.. São Paulo: USP/Pró-Reitoria de Pesquisa, 2011. Disponível em: https://sistemas.usp.br/siicusp/cdOnlineTrabalhoVisualizarResumo?numeroInscricaoTrabalho=2408&numeroEdicao=19. Acesso em: 27 abr. 2024.
APA
Bueno, C. T., Lima, L. T. de, Vivona, D., & Guerra-Shinohara, E. M. (2011). Frequency of C848T, C859G, C480G and A1222G polymorphisms in SLC22A1 gene in chronic myelogenous leukaemia patients treated with imatinib mesilate. In Resumos. São Paulo: USP/Pró-Reitoria de Pesquisa. Recuperado de https://sistemas.usp.br/siicusp/cdOnlineTrabalhoVisualizarResumo?numeroInscricaoTrabalho=2408&numeroEdicao=19
NLM
Bueno CT, Lima LT de, Vivona D, Guerra-Shinohara EM. Frequency of C848T, C859G, C480G and A1222G polymorphisms in SLC22A1 gene in chronic myelogenous leukaemia patients treated with imatinib mesilate [Internet]. Resumos. 2011 ;[citado 2024 abr. 27 ] Available from: https://sistemas.usp.br/siicusp/cdOnlineTrabalhoVisualizarResumo?numeroInscricaoTrabalho=2408&numeroEdicao=19
Vancouver
Bueno CT, Lima LT de, Vivona D, Guerra-Shinohara EM. Frequency of C848T, C859G, C480G and A1222G polymorphisms in SLC22A1 gene in chronic myelogenous leukaemia patients treated with imatinib mesilate [Internet]. Resumos. 2011 ;[citado 2024 abr. 27 ] Available from: https://sistemas.usp.br/siicusp/cdOnlineTrabalhoVisualizarResumo?numeroInscricaoTrabalho=2408&numeroEdicao=19

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