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Artigo de periodico
MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients (2017)
Horita, Melanie; Bueno, Carolina Tosin; Horimoto, Andrea R.; Lemos, Pedro A.; Morandini-Filho, Antonio A.; Krieger, José E.; Santos, Paulo C. J. L.; Pereira, Alexandre C.
Source: International Journal of Cardiology. Heart & Vasculature. Unidade: FM
Subjects: DOENÇAS CARDIOVASCULARES, BRASILEIROS, HOMOCISTEÍNA, VITAMINAS, DOENÇAS CONGÊNITAS
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ABNT
HORITA, Melanie et al. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients. International Journal of Cardiology. Heart & Vasculature, v. 14, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ijcha.2016.11.004. Acesso em: 06 nov. 2024.
APA
Horita, M., Bueno, C. T., Horimoto, A. R., Lemos, P. A., Morandini-Filho, A. A., Krieger, J. E., et al. (2017). MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients. International Journal of Cardiology. Heart & Vasculature, 14, 1-5. doi:10.1016/j.ijcha.2016.11.004
NLM
Horita M, Bueno CT, Horimoto AR, Lemos PA, Morandini-Filho AA, Krieger JE, Santos PCJL, Pereira AC. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients [Internet]. International Journal of Cardiology. Heart & Vasculature. 2017 ; 14 1-5.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijcha.2016.11.004
Vancouver
Horita M, Bueno CT, Horimoto AR, Lemos PA, Morandini-Filho AA, Krieger JE, Santos PCJL, Pereira AC. MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients [Internet]. International Journal of Cardiology. Heart & Vasculature. 2017 ; 14 1-5.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijcha.2016.11.004
Artigo de periodico
CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy (2015)
Santos, Juliana Rocha; Tomaz, Paulo Roberto Xavier; Issa, Jaqueline Scholz; Abe, Tania Ogawa; Krieger, Jose Eduardo; Pereira, Alexandre Costa; Santos, Paulo C. J. L.
Source: Frontiers in Genetics. Unidade: FM
Subjects: TABAGISMO, FÁRMACOS, FUMO, POLIMORFISMO, ABANDONO DO HÁBITO DE FUMAR
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ABNT
SANTOS, Juliana Rocha et al. CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy. Frontiers in Genetics, v. 6, p. 1-7, 2015Tradução . . Disponível em: https://doi.org/10.3389/fgene.2015.00046. Acesso em: 06 nov. 2024.
APA
Santos, J. R., Tomaz, P. R. X., Issa, J. S., Abe, T. O., Krieger, J. E., Pereira, A. C., & Santos, P. C. J. L. (2015). CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy. Frontiers in Genetics, 6, 1-7. doi:10.3389/fgene.2015.00046
NLM
Santos JR, Tomaz PRX, Issa JS, Abe TO, Krieger JE, Pereira AC, Santos PCJL. CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy [Internet]. Frontiers in Genetics. 2015 ; 6 1-7.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3389/fgene.2015.00046
Vancouver
Santos JR, Tomaz PRX, Issa JS, Abe TO, Krieger JE, Pereira AC, Santos PCJL. CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy [Internet]. Frontiers in Genetics. 2015 ; 6 1-7.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3389/fgene.2015.00046
Artigo de periodico
LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography (2014)
Santos, Paulo C. J. L.; Bueno, Carolina T.; Lemos, Pedro A.; Krieger, José E.; Pereira, Alexandre C.
Source: Lipids in Health and Disease. Unidade: FM
Subjects: POLIMORFISMO, ANGIOGRAFIA, DOENÇAS CARDIOVASCULARES, FATORES DE RISCO
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ABNT
SANTOS, Paulo C. J. L. et al. LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography. Lipids in Health and Disease, v. 13, p. 7 , 2014Tradução . . Disponível em: http://www.lipidworld.com/content/13/1/74. Acesso em: 06 nov. 2024.
APA
Santos, P. C. J. L., Bueno, C. T., Lemos, P. A., Krieger, J. E., & Pereira, A. C. (2014). LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography. Lipids in Health and Disease, 13, 7 . doi:10.1186/1476-511X-13-74
NLM
Santos PCJL, Bueno CT, Lemos PA, Krieger JE, Pereira AC. LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography [Internet]. Lipids in Health and Disease. 2014 ; 13 7 .[citado 2024 nov. 06 ] Available from: http://www.lipidworld.com/content/13/1/74
Vancouver
Santos PCJL, Bueno CT, Lemos PA, Krieger JE, Pereira AC. LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography [Internet]. Lipids in Health and Disease. 2014 ; 13 7 .[citado 2024 nov. 06 ] Available from: http://www.lipidworld.com/content/13/1/74
Artigo de periodico
BDKRB2 +9/−9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population (2012)
Alvim, Rafael de Oliveira; Santos, Paulo C. J. L.; Nascimento, Raimundo M.; Coelho, George L. L. M.; Mill, José G.; Krieger, José E.; Pereira, Alexandre C.
Source: Experimental Diabetes Research. Unidade: FM
Subjects: DIABETES MELLITUS (GENÉTICA;EPIDEMIOLOGIA), POLIMORFISMO, FATORES DE RISCO, ANTROPOMETRIA (MEDIDAS), GENÓTIPOS, BRASIL
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ABNT
ALVIM, Rafael de Oliveira et al. BDKRB2 +9/−9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population. Experimental Diabetes Research, v. 2012, p. 4 , 2012Tradução . . Disponível em: https://doi.org/10.1155/2012/480251. Acesso em: 06 nov. 2024.
APA
Alvim, R. de O., Santos, P. C. J. L., Nascimento, R. M., Coelho, G. L. L. M., Mill, J. G., Krieger, J. E., & Pereira, A. C. (2012). BDKRB2 +9/−9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population. Experimental Diabetes Research, 2012, 4 . doi:10.1155/2012/480251
NLM
Alvim R de O, Santos PCJL, Nascimento RM, Coelho GLLM, Mill JG, Krieger JE, Pereira AC. BDKRB2 +9/−9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population [Internet]. Experimental Diabetes Research. 2012 ; 2012 4 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1155/2012/480251
Vancouver
Alvim R de O, Santos PCJL, Nascimento RM, Coelho GLLM, Mill JG, Krieger JE, Pereira AC. BDKRB2 +9/−9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population [Internet]. Experimental Diabetes Research. 2012 ; 2012 4 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1155/2012/480251
Artigo de periodico
Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis (2012)
Santos, Paulo C. J. L.; Krieger, Jose E.; Pereira, Alexandre C.
Source: International Journal of Molecular Sciences. Unidade: FM
Subjects: HEMOCROMATOSE (GENÉTICA;DIAGNÓSTICO), DOENÇAS HEREDITÁRIAS (GENÉTICA;DIAGNÓSTICO), FERRO (EFEITOS ADVERSOS), BIOLOGIA MOLECULAR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo C. J. L. e KRIEGER, Jose E. e PEREIRA, Alexandre C. Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis. International Journal of Molecular Sciences, v. 13, n. 2, p. 1497-1511, 2012Tradução . . Disponível em: https://doi.org/10.3390/ijms13021497. Acesso em: 06 nov. 2024.
APA
Santos, P. C. J. L., Krieger, J. E., & Pereira, A. C. (2012). Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis. International Journal of Molecular Sciences, 13( 2), 1497-1511. doi:10.3390/ijms13021497
NLM
Santos PCJL, Krieger JE, Pereira AC. Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis [Internet]. International Journal of Molecular Sciences. 2012 ; 13( 2): 1497-1511.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/ijms13021497
Vancouver
Santos PCJL, Krieger JE, Pereira AC. Molecular Diagnostic and Pathogenesis of Hereditary Hemochromatosis [Internet]. International Journal of Molecular Sciences. 2012 ; 13( 2): 1497-1511.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/ijms13021497
Artigo de periodico
CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population (2011)
Santos, Paulo C. J. L.; Soares, Renata A. G.; Santos, Diogo B. G.; Krieger, José E.; Nicolau, José C.; Nascimento, Raimundo M.; Coelho, George L. L. M.; Mill, José G.; Pereira, Alexandre C.
Source: BMC Medical Genetics. Unidade: FM
Subjects: POLIMORFISMO, GRUPOS ÉTNICOS, FENÓTIPOS, POPULAÇÃO, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo C. J. L. et al. CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population. BMC Medical Genetics, v. 12, n. 13, p. (online), 2011Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-12-13. Acesso em: 06 nov. 2024.
APA
Santos, P. C. J. L., Soares, R. A. G., Santos, D. B. G., Krieger, J. E., Nicolau, J. C., Nascimento, R. M., et al. (2011). CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population. BMC Medical Genetics, 12( 13), (online). doi:10.1186/1471-2350-12-13
NLM
Santos PCJL, Soares RAG, Santos DBG, Krieger JE, Nicolau JC, Nascimento RM, Coelho GLLM, Mill JG, Pereira AC. CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population [Internet]. BMC Medical Genetics. 2011 ; 12( 13): (online).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2350-12-13
Vancouver
Santos PCJL, Soares RAG, Santos DBG, Krieger JE, Nicolau JC, Nascimento RM, Coelho GLLM, Mill JG, Pereira AC. CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population [Internet]. BMC Medical Genetics. 2011 ; 12( 13): (online).[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2350-12-13
Artigo de periodico
SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group (2011)
Santos, Paulo C. J. L.; Soares, Renata A. G.; Nascimento, Raimundo M.; Machado-Coelho, George L. L.; Mill, José G.; Krieger, José E.; Pereira, Alexandre C.
Source: BMC Medical Genetics. Unidade: FM
Subjects: POLIMORFISMO, ZONA URBANA, ÁREAS CENTRAIS, GENÓTIPOS, GRUPOS ÉTNICOS, MIOPATIAS CONGÊNITAS ESTRUTURAIS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo C. J. L. et al. SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group. BMC Medical Genetics, v. 12, n. 136, p. 1-6, 2011Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-12-136. Acesso em: 06 nov. 2024.
APA
Santos, P. C. J. L., Soares, R. A. G., Nascimento, R. M., Machado-Coelho, G. L. L., Mill, J. G., Krieger, J. E., & Pereira, A. C. (2011). SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group. BMC Medical Genetics, 12( 136), 1-6. doi:10.1186/1471-2350-12-136
NLM
Santos PCJL, Soares RAG, Nascimento RM, Machado-Coelho GLL, Mill JG, Krieger JE, Pereira AC. SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group [Internet]. BMC Medical Genetics. 2011 ; 12( 136): 1-6.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2350-12-136
Vancouver
Santos PCJL, Soares RAG, Nascimento RM, Machado-Coelho GLL, Mill JG, Krieger JE, Pereira AC. SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group [Internet]. BMC Medical Genetics. 2011 ; 12( 136): 1-6.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2350-12-136
Artigo de periodico
APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population (2010)
Alvim, Rafael O.; Freitas, Silvia R. S.; Santos, Paulo C. J. L.; Cunha, Roberto S.; Mill, José G.; Krieger, José Eduardo; Pereira, Alexandre C.
Source: Lipids in Health and Disease. Unidade: FM
Subjects: POLIMORFISMO, GENÓTIPOS, ESTRESSE PSICOLÓGICO, GLICOPROTEÍNAS, APOLIPOPROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVIM, Rafael O. et al. APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population. Lipids in Health and Disease, v. 9, n. 128, 2010Tradução . . Disponível em: https://doi.org/10.1186/1476-511x-9-128. Acesso em: 06 nov. 2024.
APA
Alvim, R. O., Freitas, S. R. S., Santos, P. C. J. L., Cunha, R. S., Mill, J. G., Krieger, J. E., & Pereira, A. C. (2010). APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population. Lipids in Health and Disease, 9( 128). doi:10.1186/1476-511x-9-128
NLM
Alvim RO, Freitas SRS, Santos PCJL, Cunha RS, Mill JG, Krieger JE, Pereira AC. APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population [Internet]. Lipids in Health and Disease. 2010 ; 9( 128):[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1476-511x-9-128
Vancouver
Alvim RO, Freitas SRS, Santos PCJL, Cunha RS, Mill JG, Krieger JE, Pereira AC. APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population [Internet]. Lipids in Health and Disease. 2010 ; 9( 128):[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1476-511x-9-128

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