Detalhe da pesquisa
1.
Deferasirox in patients with iron overload secondary to hereditary hemochromatosis: results of a 1-yr Phase 2 study.
Eur J Haematol
; 95(6): 545-50, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25684349
2.
General aspects of muscle glucose uptake.
An Acad Bras Cienc
; 87(1): 351-68, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25761221
3.
The MYLIP p.N342S polymorphism is associated with response to lipid-lowering therapy in Brazilian patients with familial hypercholesterolemia.
Pharmacogenet Genomics
; 24(11): 548-55, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25171759
4.
Effectiveness of coadministration of varenicline, bupropion, and serotonin reuptake inhibitors in a smoking cessation program in the real-life setting.
Nicotine Tob Res
; 15(6): 1146-50, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23128516
5.
MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population.
Lipids Health Dis
; 11: 83, 2012 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-22741812
6.
Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
Int J Mol Sci
; 13(2): 1497-1511, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22408404
7.
Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
Blood Cells Mol Dis
; 46(4): 302-7, 2011 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21411349
8.
CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population.
BMC Med Genet
; 12: 13, 2011 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21247447
9.
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 Med Genet
; 12: 136, 2011 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21992719
10.
HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
Blood Cells Mol Dis
; 45(4): 302-7, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20843714
11.
APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population.
Lipids Health Dis
; 9: 128, 2010 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21059196
12.
Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.
Clin Pharmacol Ther
; 107(6): 1420-1433, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31869433
13.
Genotype-guided warfarin therapy: current status.
Pharmacogenomics
; 19(7): 667-685, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29701078
14.
Association Between ABCB1 Polymorphism and Stable Warfarin Dose Requirements in Brazilian Patients.
Front Pharmacol
; 9: 542, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875668
15.
Two new mutations in the HIF2A gene associated with erythrocytosis.
Am J Hematol
; 87(4): 439-42, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22367913
16.
Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox.
World J Clin Cases
; 5(10): 381-383, 2017 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29085829
17.
MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients.
Int J Cardiol Heart Vasc
; 14: 1-5, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28616555
18.
CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy.
Front Genet
; 6: 46, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25774163
19.
BDKRB2 +9/-9 polymorphism is associated with higher risk for diabetes mellitus in the Brazilian general population.
Exp Diabetes Res
; 2012: 480251, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23243416
20.
Thioredoxin interacting protein genetic variation is associated with diabetes and hypertension in the Brazilian general population.
Atherosclerosis
; 221(1): 131-6, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22236479