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Alexandre C Pereira

Showing results (31-40 of 348) with videos related to

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Journal of Negative Results in Biomedicine|January 13, 2012
A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathyDiogo G Biagi, José G Mill, Alfredo J Mansur, et al.
BMC Medical Genetics|September 22, 2010
Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian familiesSuely R Giolo, Alexandre C Pereira, Mariza de Andrade, et al.
Journal of Diabetes and Its Complications|March 10, 2009
Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese BraziliansMarcio F Vendramini, Alexandre C Pereira, Sandra R Ferreira, et al.
Thrombosis Research|January 13, 2006
Association between platelet P2Y12 haplotype and risk of cardiovascular events in chronic coronary diseaseIsolmar T Schettert, Alexandre C Pereira, Neuza H Lopes, et al.
Journal of Nephrology|July 29, 2006
NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosisEduardo J B Monteiro, Alexandre C Pereira, Aparecido B Pereira, et al.
BMC Medical Genetics|April 24, 2008
Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart StudyCamila M de Oliveira, Alexandre C Pereira, Mariza de Andrade, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|November 7, 2012
Effectiveness of coadministration of varenicline, bupropion, and serotonin reuptake inhibitors in a smoking cessation program in the real-life settingJaqueline S Issa, Tania Ogawa Abe, Simone Moura, et al.
Genetic Epidemiology|January 14, 2014
Using item response theory to model multiple phenotypes and their joint heritability in family dataTiago M Fragoso, Suely R Giolo, Alexandre C Pereira, et al.
Plos One|February 2, 2011
Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery diseaseAndré Gustavo P Sousa, Neuza H Lopes, Whady A Hueb, et al.
Arquivos Brasileiros De Cardiologia|September 10, 2002
Arterial hypertension in a child with Williams-Beuren syndrome (7q11.23 chromosomal deletion)Cristina de Sylos, Alexandre C Pereira, Estela Azeka, et al.
Pageof 35

Showing results (31-40 of 348) with videos related to

Sort By:
Pageof 35
Journal of Negative Results in Biomedicine|January 13, 2012
A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathyDiogo G Biagi, José G Mill, Alfredo J Mansur, et al.
BMC Medical Genetics|September 22, 2010
Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian familiesSuely R Giolo, Alexandre C Pereira, Mariza de Andrade, et al.
Journal of Diabetes and Its Complications|March 10, 2009
Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese BraziliansMarcio F Vendramini, Alexandre C Pereira, Sandra R Ferreira, et al.
Thrombosis Research|January 13, 2006
Association between platelet P2Y12 haplotype and risk of cardiovascular events in chronic coronary diseaseIsolmar T Schettert, Alexandre C Pereira, Neuza H Lopes, et al.
Journal of Nephrology|July 29, 2006
NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosisEduardo J B Monteiro, Alexandre C Pereira, Aparecido B Pereira, et al.
BMC Medical Genetics|April 24, 2008
Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart StudyCamila M de Oliveira, Alexandre C Pereira, Mariza de Andrade, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|November 7, 2012
Effectiveness of coadministration of varenicline, bupropion, and serotonin reuptake inhibitors in a smoking cessation program in the real-life settingJaqueline S Issa, Tania Ogawa Abe, Simone Moura, et al.
Genetic Epidemiology|January 14, 2014
Using item response theory to model multiple phenotypes and their joint heritability in family dataTiago M Fragoso, Suely R Giolo, Alexandre C Pereira, et al.
Plos One|February 2, 2011
Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery diseaseAndré Gustavo P Sousa, Neuza H Lopes, Whady A Hueb, et al.
Arquivos Brasileiros De Cardiologia|September 10, 2002
Arterial hypertension in a child with Williams-Beuren syndrome (7q11.23 chromosomal deletion)Cristina de Sylos, Alexandre C Pereira, Estela Azeka, et al.
Pageof 35