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Artigo de periodico
Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer (2011)
López, R. V. M; Zago, Marco Antonio; Eluf Neto, José; Curado, M. P.; Daudt, A W.; Silva Júnior, Wilson Araújo da; Zanette, D. L.; Levi, J. E.; Carvalho, M. B. de; Kowalski, L. P.; Abrahão, M.; Góis-Filho, J. F. de; Boffetta, P.; Wunsch Filho, Victor
Source: Brazilian Journal of Medical and Biological Research. Unidades: FMRP, FM, FSP
Subjects: NEOPLASIAS DE CABEÇA E PESCOÇO (RELAÇÃO), EDUCAÇÃO, ALCOOLISMO, TABAGISMO, POLIMORFISMO
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ABNT
LÓPEZ, R. V. M et al. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer. Brazilian Journal of Medical and Biological Research, v. 44, n. 10, p. 1006-1012, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500097. Acesso em: 26 jun. 2024.
APA
López, R. V. M., Zago, M. A., Eluf Neto, J., Curado, M. P., Daudt, A. W., Silva Júnior, W. A. da, et al. (2011). Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer. Brazilian Journal of Medical and Biological Research, 44( 10), 1006-1012. doi:10.1590/S0100-879X2011007500097
NLM
López RVM, Zago MA, Eluf Neto J, Curado MP, Daudt AW, Silva Júnior WA da, Zanette DL, Levi JE, Carvalho MB de, Kowalski LP, Abrahão M, Góis-Filho JF de, Boffetta P, Wunsch Filho V. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 10): 1006-1012.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/S0100-879X2011007500097
Vancouver
López RVM, Zago MA, Eluf Neto J, Curado MP, Daudt AW, Silva Júnior WA da, Zanette DL, Levi JE, Carvalho MB de, Kowalski LP, Abrahão M, Góis-Filho JF de, Boffetta P, Wunsch Filho V. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 10): 1006-1012.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/S0100-879X2011007500097
Artigo de periodico
Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil (2006)
Wünsch-Filho, V.; Eluf Neto, José; Lotufo, P. A.; Silva Junior, W. A.; Zago, M. A.
Source: Brazilian Journal of Medical and Biological Research. Unidades: FSP, FM, HU, FMRP
Subjects: NEOPLASIAS (ESTUDO), EPIDEMIOLOGIA (CLASSIFICAÇÃO;GENÉTICA), GENOMAS (EPIDEMIOLOGIA), SAÚDE PÚBLICA
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ABNT
WÜNSCH-FILHO, V. et al. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil. Brazilian Journal of Medical and Biological Research, v. 39, n. 4, p. 545-553, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2006000400016. Acesso em: 26 jun. 2024.
APA
Wünsch-Filho, V., Eluf Neto, J., Lotufo, P. A., Silva Junior, W. A., & Zago, M. A. (2006). Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil. Brazilian Journal of Medical and Biological Research, 39( 4), 545-553. doi:10.1590/s0100-879x2006000400016
NLM
Wünsch-Filho V, Eluf Neto J, Lotufo PA, Silva Junior WA, Zago MA. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 545-553.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2006000400016
Vancouver
Wünsch-Filho V, Eluf Neto J, Lotufo PA, Silva Junior WA, Zago MA. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 545-553.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2006000400016
Artigo de periodico
The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample (2003)
Scartezini, M.; Zago, Marco Antônio; Chautard-Freire-Maia, E. A.; Pazin-Filho, Antônio; Marin-Neto, José Antônio; Hotta, Júlia Keiko Sakamoto; Nascimento, A. J.; Santos, José Ernesto dos
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: POLIMORFISMO, FATORES DE RISCO, CORONARIOPATIA
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ABNT
SCARTEZINI, M. et al. The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample. Brazilian Journal of Medical and Biological Research, v. 36, n. 3, p. 369-375, 2003Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2003000300012. Acesso em: 26 jun. 2024.
APA
Scartezini, M., Zago, M. A., Chautard-Freire-Maia, E. A., Pazin-Filho, A., Marin-Neto, J. A., Hotta, J. K. S., et al. (2003). The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample. Brazilian Journal of Medical and Biological Research, 36( 3), 369-375. doi:10.1590/s0100-879x2003000300012
NLM
Scartezini M, Zago MA, Chautard-Freire-Maia EA, Pazin-Filho A, Marin-Neto JA, Hotta JKS, Nascimento AJ, Santos JE dos. The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36( 3): 369-375.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2003000300012
Vancouver
Scartezini M, Zago MA, Chautard-Freire-Maia EA, Pazin-Filho A, Marin-Neto JA, Hotta JKS, Nascimento AJ, Santos JE dos. The X-X-/E+E+ genotype of the Xbal/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36( 3): 369-375.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2003000300012
Artigo de periodico
HFE gene mutations in coronary atherothrombotic disease (2000)
Calado, R T; Franco, R F; Pazin Filho, A; Simões, Marcus Vinícius; Marin-Neto, José Antônio; Zago, Marco Antônio
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: CARDIOPATIAS
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ABNT
CALADO, R T et al. HFE gene mutations in coronary atherothrombotic disease. Brazilian Journal of Medical and Biological Research, v. 33, n. 3, p. 301-306, 2000Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2000000300007. Acesso em: 26 jun. 2024.
APA
Calado, R. T., Franco, R. F., Pazin Filho, A., Simões, M. V., Marin-Neto, J. A., & Zago, M. A. (2000). HFE gene mutations in coronary atherothrombotic disease. Brazilian Journal of Medical and Biological Research, 33( 3), 301-306. doi:10.1590/s0100-879x2000000300007
NLM
Calado RT, Franco RF, Pazin Filho A, Simões MV, Marin-Neto JA, Zago MA. HFE gene mutations in coronary atherothrombotic disease [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 3): 301-306.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2000000300007
Vancouver
Calado RT, Franco RF, Pazin Filho A, Simões MV, Marin-Neto JA, Zago MA. HFE gene mutations in coronary atherothrombotic disease [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 3): 301-306.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x2000000300007
Artigo de periodico
The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil (1999)
Alberto, Fernando Lopes; Figueiredo, Mauro Silvério; Zago, Marco Antônio; Araújo, A. G.; Santos, José Ernesto dos
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, MUTAGÊNESE
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ABNT
ALBERTO, Fernando Lopes et al. The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil. Brazilian Journal of Medical and Biological Research, v. 32, n. 6, p. 739-745, 1999Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x1999000600009. Acesso em: 26 jun. 2024.
APA
Alberto, F. L., Figueiredo, M. S., Zago, M. A., Araújo, A. G., & Santos, J. E. dos. (1999). The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil. Brazilian Journal of Medical and Biological Research, 32( 6), 739-745. doi:10.1590/s0100-879x1999000600009
NLM
Alberto FL, Figueiredo MS, Zago MA, Araújo AG, Santos JE dos. The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 1999 ; 32( 6): 739-745.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x1999000600009
Vancouver
Alberto FL, Figueiredo MS, Zago MA, Araújo AG, Santos JE dos. The lebanese mutation as an important cause of familial hypercholesterolemia in Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 1999 ; 32( 6): 739-745.[citado 2024 jun. 26 ] Available from: https://doi.org/10.1590/s0100-879x1999000600009
Artigo de periodico
B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil (1991)
Costa, F F; Tavella, M H; Zago, M A
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: MEDICINA INTERNA
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ABNT
COSTA, F F e TAVELLA, M H e ZAGO, M A. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research, v. 24, p. 157-61, 1991Tradução . . Acesso em: 26 jun. 2024.
APA
Costa, F. F., Tavella, M. H., & Zago, M. A. (1991). B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research, 24, 157-61.
NLM
Costa FF, Tavella MH, Zago MA. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research. 1991 ;24 157-61.[citado 2024 jun. 26 ]
Vancouver
Costa FF, Tavella MH, Zago MA. B-thalassemia intermedia and ivs - 1 nt6 homozygosis in brazil. Brazilian Journal of Medical and Biological Research. 1991 ;24 157-61.[citado 2024 jun. 26 ]
Artigo de periodico
Hemoglobin h disease caused by two gene deletions (1989)
Zago, M A; Paço-Larson, Maria Luísa
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: MEDICINA
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ABNT
ZAGO, M A e PAÇO-LARSON, Maria Luísa. Hemoglobin h disease caused by two gene deletions. Brazilian Journal of Medical and Biological Research, v. 22, p. 675-81, 1989Tradução . . Acesso em: 26 jun. 2024.
APA
Zago, M. A., & Paço-Larson, M. L. (1989). Hemoglobin h disease caused by two gene deletions. Brazilian Journal of Medical and Biological Research, 22, 675-81.
NLM
Zago MA, Paço-Larson ML. Hemoglobin h disease caused by two gene deletions. Brazilian Journal of Medical and Biological Research. 1989 ;22 675-81.[citado 2024 jun. 26 ]
Vancouver
Zago MA, Paço-Larson ML. Hemoglobin h disease caused by two gene deletions. Brazilian Journal of Medical and Biological Research. 1989 ;22 675-81.[citado 2024 jun. 26 ]
Artigo de periodico
Evaluation of spleen function in man (1989)
Zago, M A
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: MEDICINA
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ABNT
ZAGO, M A. Evaluation of spleen function in man. Brazilian Journal of Medical and Biological Research, v. 22, p. 159-69, 1989Tradução . . Acesso em: 26 jun. 2024.
APA
Zago, M. A. (1989). Evaluation of spleen function in man. Brazilian Journal of Medical and Biological Research, 22, 159-69.
NLM
Zago MA. Evaluation of spleen function in man. Brazilian Journal of Medical and Biological Research. 1989 ;22 159-69.[citado 2024 jun. 26 ]
Vancouver
Zago MA. Evaluation of spleen function in man. Brazilian Journal of Medical and Biological Research. 1989 ;22 159-69.[citado 2024 jun. 26 ]
Artigo de periodico
G-gamma levels of the hbf of patients with bone marrow failure syndromes (1987)
Zago, M A
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ANEMIA, CRIANÇAS EM IDADE PRÉ-ESCOLAR, CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO
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ABNT
ZAGO, M A. G-gamma levels of the hbf of patients with bone marrow failure syndromes. Brazilian Journal of Medical and Biological Research, v. 20, p. 363-8, 1987Tradução . . Acesso em: 26 jun. 2024.
APA
Zago, M. A. (1987). G-gamma levels of the hbf of patients with bone marrow failure syndromes. Brazilian Journal of Medical and Biological Research, 20, 363-8.
NLM
Zago MA. G-gamma levels of the hbf of patients with bone marrow failure syndromes. Brazilian Journal of Medical and Biological Research. 1987 ;20 363-8.[citado 2024 jun. 26 ]
Vancouver
Zago MA. G-gamma levels of the hbf of patients with bone marrow failure syndromes. Brazilian Journal of Medical and Biological Research. 1987 ;20 363-8.[citado 2024 jun. 26 ]

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