Browsing by Author "Menezes, Joelma Figueiredo"
Now showing items 1-10 of 10
-
C677T polymorphism of the MTHFR gene and variant hemoglobins: a study in newborns from Salvador, Bahia, Brazil
Couto, Fábio David et al. | Date Issued: 2004 -
Hemoglobinopathies in newborns from Salvador, Bahia, Northeast Brazil.
Adorno, Elisângela Vitória et al. | Date Issued: 2005Hemoglobinopatias são alterações hereditárias na molécula de hemoglobina com prevalência mundial elevada. O Brasil apresenta prevalência de 0,1 a 0,3% para recém-nascidos com anemia falciforme e freqüência de 20,0 a ... -
Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease
Seixas, Magda Oliveira et al. | Date Issued: 2010 -
Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease.
Seixas, Magda Oliveira et al. | Date Issued: 2010 -
Performance of microscopy and ELISA for diagnosing Giardia duodenalis infection in different pediatric groups
Silva, Renata K N R et al. | Date Issued: 2016 -
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease
Menezes, Joelma Figueiredo et al. | Date Issued: 2023 -
Sickle cell disease sc in northeast of Brazil: a clinical and molecular characterization
Cajado, Cyntia et al. | Date Issued: 2010doença SC é muito prevalente no Brasil, principalmente na Bahia, sendo que os pacientes apresentam anemia grave, mas com menos complicações clínicas que os homozigotos SS. Os pacientes com doença de SC têm menos crises ... -
The beta-globin gene cluster haplotypes in sickle cell anemia patients from Northeast Brazil: a clinical and molecular view.
Adorno, Elisângela Vitória et al. | Date Issued: 2004 -
The beta-globin gene cluster haplotypes in sickle cell anemia patients from Northeast Brazil: a clinical and molecular view.
Adorno, Elisângela Vitória et al. | Date Issued: 2004 -
The C282Y and H63D mutations in the haemochromatosis gene among sickle cell anemia patients from the Northeast of Brazil
Menezes, Joelma Figueiredo et al. | Date Issued: 2010A Hemocromatose Hereditária (HH) é uma doença autossômica recessiva. As mutações C282Y e H63D no gene HFE têm sido associadas à HH. Objetivo: Avaliar as frequências das mutações C282Y e H63D em pacientes com anemia ...