Browsing by Author "Gonçalves, Marilda de Souza"
Now showing items 146-165 of 182
-
Priapismo na doença falciforme: associação entre polimorfismos genéticos e biomarcadores laboratoriais
Figueiredo, Camylla Vilas Boas | Date Issued: 2019INTRODUÇÃO: A doença falciforme (DF) é constituída por um grupo de doenças hematológicas que têm em comum a presença da hemoglobina variante S (HbS), sendo a anemia falciforme (AF) a forma mais grave da doença, e a ... -
Renal hemosiderosis complicating sickle cell anemia
Calazans, Leonardo M et al. | Date Issued: 2012 -
Risk factors for Toxocara spp. seroprevalence and its association withatopy and asthma phenotypes in school-age children in a small town and semi-rural areas of Northeast Brazil
Silva, Márcia B et al. | Date Issued: 2016 -
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 -
Short communication: phylodynamics analysis of the human immunodeficiency virus type 1 envelope gene in mother and child pairs
Santos, Luciane Amorim et al. | Date Issued: 2015 -
Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2018 -
Sickle cell anemia: delayed diagnosis in Bahia, Brazil-a largely Afro-descendant population
Zanette, Angela Maria Dias et al. | Date Issued: 2011 -
Sickle cell disease retinopathy: characterization among pediatric and teenage patients from northeastern Brazil
Oliveira, Dayse Cury de Almeida et al. | Date Issued: 2014 -
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 ... -
Soroprevalência de anticorpos anti-toxocara SPPEM Município do Recôncavo Baiano
Silva, Márcia Barbosa da et al. | Date Issued: 2013 -
Suscetibilidade de clones isolados da cepa colombiana do Trypanosoma cruzi ao tratamento com Benzonidazol. Avaliação da reação em cadeia da polimerase (PCR) como teste de cura
Camandaroba, Edson Luiz Paes et al. | Date Issued: 2000 -
TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia
Santiago, Rayra Pereira et al. | Date Issued: 2020 -
The association of infection and clinical severity in sickle cell anaemia patients.
Moura Neto, José Pereira de et al. | Date Issued: 2011 -
The Ay-195 (C®G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro
Schreiber, R et al. | Date Issued: 2001 -
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 ... -
The host genetic diversity in malaria infection
Mendonça, Vitor Rosa Ramos de et al. | Date Issued: 2012 -
The leftward deletion 4.2 KB alpha-thalassemia in two sickle cell anemia siblings
Takahashi, Daniele et al. | Date Issued: 2010A presença da deleção –α thal 3.7Kb está associada com melhor prognóstico de pacientes que possuem anemia falciforme (AF), contudo não existem estudos na literatura a respeito da associação da –α thal 4.2Kb com a evolução ...