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Artigo de periodico
Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationale (2014)
Gioli-Pereira, Luciana; Bernardez-Pereira, Sabrina; Marcondes-Braga, Fabiana Goulart; Spina, Joceli Mabel Rocha; Silva, Rafael Muniz Miranda da; Ferreira, Noely Evangelista; Bacal, Fernando; Fernandes, Fábio; Mansur, Alfredo José; Krieger, José Eduardo; Pereira, Alexandre Costa
Source: BMC cardiovascular disorders. Unidade: FM
Subjects: GENOMAS, GENÉTICA, DOENÇAS CARDIOVASCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIOLI-PEREIRA, Luciana et al. Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationale. BMC cardiovascular disorders, v. 14, n. 32, p. 5 2014, 2014Tradução . . Disponível em: https://doi.org/10.1186/1471-2261-14-32. Acesso em: 06 nov. 2024.
APA
Gioli-Pereira, L., Bernardez-Pereira, S., Marcondes-Braga, F. G., Spina, J. M. R., Silva, R. M. M. da, Ferreira, N. E., et al. (2014). Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationale. BMC cardiovascular disorders, 14( 32), 5 2014. doi:10.1186/1471-2261-14-32
NLM
Gioli-Pereira L, Bernardez-Pereira S, Marcondes-Braga FG, Spina JMR, Silva RMM da, Ferreira NE, Bacal F, Fernandes F, Mansur AJ, Krieger JE, Pereira AC. Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationale [Internet]. BMC cardiovascular disorders. 2014 ; 14( 32): 5 2014.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2261-14-32
Vancouver
Gioli-Pereira L, Bernardez-Pereira S, Marcondes-Braga FG, Spina JMR, Silva RMM da, Ferreira NE, Bacal F, Fernandes F, Mansur AJ, Krieger JE, Pereira AC. Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationale [Internet]. BMC cardiovascular disorders. 2014 ; 14( 32): 5 2014.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2261-14-32
Artigo de periodico
Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 (2012)
Gioli-Pereira, Luciana; Santos, Paulo Caleb Junior L; Ferreira, Noely Evangelista; Hueb, Whady A; Krieger, José Eduardo; Pereira, Alexandre C
Source: BMC Cardiovascular Disorders. Unidade: FM
Subjects: CORONARIOPATIA (EPIDEMIOLOGIA;MORTALIDADE;GENÉTICA), POLIMORFISMO, CROMOSSOMOS (PATOLOGIA), DOENÇAS CARDIOVASCULARES (EPIDEMIOLOGIA;MORTALIDADE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIOLI-PEREIRA, Luciana et al. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21. BMC Cardiovascular Disorders, v. 12, p. 7 , 2012Tradução . . Disponível em: https://doi.org/10.1186/1471-2261-12-61. Acesso em: 06 nov. 2024.
APA
Gioli-Pereira, L., Santos, P. C. J. L., Ferreira, N. E., Hueb, W. A., Krieger, J. E., & Pereira, A. C. (2012). Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21. BMC Cardiovascular Disorders, 12, 7 . doi:10.1186/1471-2261-12-61
NLM
Gioli-Pereira L, Santos PCJL, Ferreira NE, Hueb WA, Krieger JE, Pereira AC. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 [Internet]. BMC Cardiovascular Disorders. 2012 ; 12 7 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2261-12-61
Vancouver
Gioli-Pereira L, Santos PCJL, Ferreira NE, Hueb WA, Krieger JE, Pereira AC. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 [Internet]. BMC Cardiovascular Disorders. 2012 ; 12 7 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/1471-2261-12-61
Artigo de periodico
NKX2.5 mutations in patients with non-syndromic congenital heart disease (2010)
Gioli-Pereira, Luciana; Pereira, Alexandre Costa; Mesquita, Sônia M.; Xavier-Neto, José; Lopes, Antônio Augusto; Krieger, José Eduardo
Source: International Journal of Cardiology. Unidade: FM
Subjects: COÔNIAS, CARDIOPATIAS CONGÊNITAS (GENÉTICA), MUTAÇÃO GENÊTICA, GENES (ANÁLISE), REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIOLI-PEREIRA, Luciana et al. NKX2.5 mutations in patients with non-syndromic congenital heart disease. International Journal of Cardiology, v. 138, n. 3, p. 261-265, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ijcard.2008.08.035. Acesso em: 06 nov. 2024.
APA
Gioli-Pereira, L., Pereira, A. C., Mesquita, S. M., Xavier-Neto, J., Lopes, A. A., & Krieger, J. E. (2010). NKX2.5 mutations in patients with non-syndromic congenital heart disease. International Journal of Cardiology, 138( 3), 261-265. doi:10.1016/j.ijcard.2008.08.035
NLM
Gioli-Pereira L, Pereira AC, Mesquita SM, Xavier-Neto J, Lopes AA, Krieger JE. NKX2.5 mutations in patients with non-syndromic congenital heart disease [Internet]. International Journal of Cardiology. 2010 ; 138( 3): 261-265.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijcard.2008.08.035
Vancouver
Gioli-Pereira L, Pereira AC, Mesquita SM, Xavier-Neto J, Lopes AA, Krieger JE. NKX2.5 mutations in patients with non-syndromic congenital heart disease [Internet]. International Journal of Cardiology. 2010 ; 138( 3): 261-265.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijcard.2008.08.035

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