Lista de obras -

Association between interferon lambda 3 rs12979860 polymorphism and clinical outcome in dengue virus-infected children

artículo científico publicado en 2020

Association of Catalase and Glutathione Peroxidase 1 Polymorphisms with Chronic Hepatitis C Outcome

artículo científico publicado en 2016

Association of the MBL2 gene EXON1 polymorphism and vasoocclusive crisis in patients with sickle cell anemia.

artículo científico publicado en 2009

Association of variant alleles of MBL2 gene with vasoocclusive crisis in children with sickle cell anemia.

artículo científico publicado en 2010

Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia

artículo científico publicado en 2017

Does physical exercise influence in the development of neuroeschistosomiasis?

artículo científico publicado en 2019

Expression of microRNAs (133b and 138) and Correlation with Echocardiographic Parameters in Patients with Alcoholic Cardiomyopathy

artículo científico publicado en 2020

Genetic variation in PTX3 and plasma levels associated with hepatocellular carcinoma in patients with HCV.

artículo científico publicado en 2015

High tumor necrosis factor-α/interleukin-10 ratio is associated with hepatocellular carcinoma in patients with chronic hepatitis C.

artículo científico publicado en 2013

IL17A Polymorphism Is Not Associated with Human T-Lymphotropic Virus 1-Associated Myelopathy/Tropical Spastic Paraparesis

artículo científico publicado en 2017

Lack of association between the Duffy antigen receptor for chemokines (DARC) expression and clinical outcome of children with sickle cell anemia.

artículo científico publicado en 2015

Low IL10 serum levels as key factor for predicting the sustained virological response to IFNα/ribavirin in Brazilian patients with HCV carrying IL28B CT/TT genotype.

artículo científico publicado en 2014

Mannose-binding lectin 2 (MBL2) gene polymorphisms do not influence frequency of infections in chronic lymphocytic leukemia patients

artículo científico publicado en 2014

Mannose-binding lectin serum levels in patients with leprosy are influenced by age and MBL2 genotypes

artículo científico publicado en 2011

Molecular profile of mannan-binding lectin in hepatitis C patients with MBL gene polymorphisms by a modified mannan-coated nitrocellulose assay

article

Myeloperoxidase gene polymorphism predicts fibrosis severity in women with hepatitis C.

artículo científico publicado en 2014

Plasma myeloperoxidase levels correlate with hepatocellular carcinoma in chronic hepatitis C.

artículo científico publicado en 2012

Polymorphisms of CYP2C92, CYP2C93 and VKORC1 genes related to time in therapeutic range in patients with atrial fibrillation using warfarin

scientific article published on 02 August 2019

Structural polymorphism of the mannose-binding lectin 2 (MBL2 ) gene in HCV-infected patients with a serological marker for thyroid autoimmunity.

artículo científico publicado en 2009

Two sides of a coin: GG genotype of C7 provides protection against fibrosis severity while showing a higher risk for hepatocellular carcinoma in patients with hepatitis C

artículo científico publicado en 2018

Lista de obras de

Association between interferon lambda 3 rs12979860 polymorphism and clinical outcome in dengue virus-infected children

Association of Catalase and Glutathione Peroxidase 1 Polymorphisms with Chronic Hepatitis C Outcome

Association of the MBL2 gene EXON1 polymorphism and vasoocclusive crisis in patients with sickle cell anemia.

Association of variant alleles of MBL2 gene with vasoocclusive crisis in children with sickle cell anemia.

Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia

Does physical exercise influence in the development of neuroeschistosomiasis?

Expression of microRNAs (133b and 138) and Correlation with Echocardiographic Parameters in Patients with Alcoholic Cardiomyopathy

Genetic variation in PTX3 and plasma levels associated with hepatocellular carcinoma in patients with HCV.

High tumor necrosis factor-α/interleukin-10 ratio is associated with hepatocellular carcinoma in patients with chronic hepatitis C.

IL17A Polymorphism Is Not Associated with Human T-Lymphotropic Virus 1-Associated Myelopathy/Tropical Spastic Paraparesis

Lack of association between the Duffy antigen receptor for chemokines (DARC) expression and clinical outcome of children with sickle cell anemia.

Low IL10 serum levels as key factor for predicting the sustained virological response to IFNα/ribavirin in Brazilian patients with HCV carrying IL28B CT/TT genotype.

Mannose-binding lectin 2 (MBL2) gene polymorphisms do not influence frequency of infections in chronic lymphocytic leukemia patients

Mannose-binding lectin serum levels in patients with leprosy are influenced by age and MBL2 genotypes

Molecular profile of mannan-binding lectin in hepatitis C patients with MBL gene polymorphisms by a modified mannan-coated nitrocellulose assay

Myeloperoxidase gene polymorphism predicts fibrosis severity in women with hepatitis C.

Plasma myeloperoxidase levels correlate with hepatocellular carcinoma in chronic hepatitis C.

Polymorphisms of CYP2C9*2, CYP2C9*3 and VKORC1 genes related to time in therapeutic range in patients with atrial fibrillation using warfarin

Structural polymorphism of the mannose-binding lectin 2 (MBL2 ) gene in HCV-infected patients with a serological marker for thyroid autoimmunity.

Two sides of a coin: GG genotype of C7 provides protection against fibrosis severity while showing a higher risk for hepatocellular carcinoma in patients with hepatitis C

Polymorphisms of CYP2C92, CYP2C93 and VKORC1 genes related to time in therapeutic range in patients with atrial fibrillation using warfarin