Browsing by Author "Moura Neto, José Pereira de"
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Bases moleculares da deficiência da dresidrogenase da glicose 6-fosfato e sua associação com hemoglobinas variantes em um grupo de recém-nascidos da cidade de Salvador-Bahia
Moura Neto, José Pereira de | Date Issued: 2004A deficiência da G6PD é uma doença hereditária ligada ao cromossomo X, caracterizada pela presença de crises hemolíticas. Investigamos as características hematológicas, eletroforéticas e moleculares da deficiência da G6PD ... -
Basic biochemical and hematological parameters of structural hemoglobin variants in the postpartum women and their respective newborn from Manaus, Amazonas, Brazil
Brito, Roberta da Silva et al. | Date Issued: 2022 -
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 -
Detection of Common Deletional of α-Thalassemia 3.7 Kb from Metropolitan Region of Manaus, Amazonas, Brazil
Cozendey, Fernanda Anselmo et al. | Date Issued: 2021 -
Diversidade fenotípica de polimorfismos na região controladora do locus(LCR) do gene da globina beta na anemia falcifore
Moura Neto, José Pereira de | Date Issued: 2010Os indivíduos com anemia falciforme (AF) possuem perfil clínico heterogêneo em função de fatores variados que contribuem para a modulação da doença, como a concentração de hemoglobina fetal (HbF), presença de haplótipos ... -
Evaluating glutathione S-transferase (GST) null genotypes (GSTT1 and GSTM1) as a potential biomarker of predisposition for developing leukopenia.
Gonçalves, Marilda de Souza et al. | Date Issued: 2010 -
G6PD deficiency in blood donors of Manaus, Amazon Region, northern Brazil
Ferreira, Natália Santos et al. | Date Issued: 2021 -
A genome survey of Moniliophthora perniciosa gives new insights into Witches' Broom Disease of cacao
Mondego, Jorge Mauricio Costa et al. | Date Issued: 2008 -
Glutathione S-transferase, catalase, and mitochondrial superoxide dismutase gene polymorphisms modulate redox potential in systemic lupus erythematosus patients from Manaus, Amazonas, Brazil
Oliveira, Marco Aurélio Almeida de et al. | Date Issued: 2021 -
GSTP1 rs1695 and rs1871042, and SOD2 rs4880 as molecular markers of lipid peroxidation in blood storage
Nascimento, Marcelo Reis do et al. | Date Issued: 2021 -
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 ... -
HTLV type 1 molecular study in Brazilian villages with African characteristics giving support to the post-Columbian introduction hypothesis.
Rego, Filipe Ferreira de Almeida et al. | Date Issued: 2008 -
Methylenetetrahydrofolate reductase polymorphisms in myeloid leukemia patients from Northeastern Brazil
Barbosa, Cynara Gomes et al. | Date Issued: 2008 -
A novel c.197T -> A variant among Brazilian neonates with glucose-6-phosphate dehydrogenase deficiency
Moura Neto, José Pereira de et al. | Date Issued: 2008 -
Outcome of B-Cell Acute Lymphoblastic Leukemia in Brazilian Children: Immunophenotypical, Hematological, and Clinical Evaluation
Cézar, Rodrigo S. et al. | Date Issued: 2015 -
Polymorphisms in the glutathione S-transferase theta and mu genes and susceptibility to myeloid leukemia in Brazilian patients
Souza, Claudio Lima et al. | Date Issued: 2008 -
Sequence change in the HS2-LCR and Gg-globin gene promoter region of sickle cell anemia patients
Adorno, Elisângela Vitória et al. | Date Issued: 2008 -
Seroprevalence and molecular epidemiology study of the HTLV-1 isolates from three villages of the São Francisco Valley, Bahia, Brazil
Rego, Filipe Ferreira de Almeida et al. | Date Issued: 2006 -
The association of infection and clinical severity in sickle cell anaemia patients.
Moura Neto, José Pereira de et al. | Date Issued: 2011 -
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 ...