LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography

Por Santos, Paulo CJL, Bueno, Carolina T, Lemos, Pedro A, Krieger, José E, Pereira, Alexandre C
Publicado em 2014

Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease

Por Gioli-Pereira, Luciana, Santos, Paulo CJL, Sugaya, Luisa S, Ferreira, Noely E, Krieger, José Eduardo, Pereira, Alexandre C, Hueb, Whady A
Publicado em 2013

The MYLIP p.N342S polymorphism is associated with response to lipid-lowering therapy in Brazilian patients with familial hypercholesterolemia

Por Santos, Paulo C.J.L., Morgan, Aline C., Jannes, Cinthia E., Krieger, José E., Santos, Raul D., Pereira, Alexandre C.
Publicado em 2014

SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high...

Por Santos, Paulo CJL, Soares, Renata AG, Nascimento, Raimundo M, Machado-Coelho, George LL, Mill, José G, Krieger, José E, Pereira, Alexandre C
Publicado em 2011

<it>APOE </it>polymorphism is associated with lipid profile, but not with arterial stiffness in the general population

Por Mill José G, Cunha Roberto S, Santos Paulo CJL, Ferreira Noely E, Freitas Silvia RS, Alvim Rafael O, Krieger José E, Pereira Alexandre C
Publicado em 2010-11-01

APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population

Por Alvim, Rafael O, Freitas, Silvia RS, Ferreira, Noely E, Santos, Paulo CJL, Cunha, Roberto S, Mill, José G, Krieger, José E, Pereira, Alexandre C
Publicado em 2010

CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population

Por Santos, Paulo CJL, Soares, Renata AG, Santos, Diogo BG, Nascimento, Raimundo M, Coelho, George LLM, Nicolau, José C, Mill, José G, Krieger, José E, Pereira, Alexandre C
Publicado em 2011

Two new mutations in the HIF2A gene associated with erythrocytosis()

Por Percy, Melanie J., Chung, Yu Jin, Harrison, Claire, Mercieca, Jane, Hoffbrand, A. Victor, Dinardo, Carla L., Santos, Paulo C.J.L., Fonseca, Guilherme H.H., Gualandro, Sandra F.M., Pereira, Alexandre C., Lappin, Terence R.J., McMullin, Mary Frances, Lee, Frank S.
Publicado em 2012