Fetal Hemoglobin
Mostrando 1-12 de 197 artigos, teses e dissertações.
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1. Epidemiology and risk factors of transfusion transmitted infections in thalassemia major: a multicenter study in Pakistan
ABSTRACT Background: Blood transfusion-transmitted infections in individuals suffering from beta-thalassemia have been reported in Pakistan, but the information on their sociodemographic and clinical determinants is lacking. This study aims to describe the prevalence, as well as the factors, contributing in blood transfusion-transmitted infections. Method:
Hematol., Transfus. Cell Ther.. Publicado em: 25/11/2019
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2. Pregnancy in Women with Complex Congenital Heart Disease. A Constant Challenge
Resumo Fundamento: A contínua habilidade na conduta das cardiopatias congênitas complexas (CCC) tem permitido o alcance da idade fértil. Contudo, a heterogeneidade das lesões cardíacas na idade adulta limita a estimativa do prognóstico da gravidez. Objetivo: Estudar a evolução materno-fetal das gestantes portadoras de CCC e analisar as variáveis p
Arq. Bras. Cardiol.. Publicado em: 03/10/2019
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3. BLOOD CELLS PROFILE IN UMBILICAL CORD OF LATE PRETERM AND TERM NEWBORNS
RESUMO Objetivo: Descrever o perfil hematológico em sangue de cordão de recém-nascidos pré-termo tardio e a termo e comparar parâmetros hematimétricos segundo sexo, adequação peso idade gestacional e tipo de parto. Métodos: Estudo transversal com recém-nascidos pré-termo tardio e a termo, em maternidade de nível secundário. Excluíram-se ges
Rev. paul. pediatr.. Publicado em: 19/06/2019
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4. Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
ABSTRACT Objective: The aim of this study was to evaluate the relationship between inflammatory cytokines, placental weight, glycated hemoglobin and adverse perinatal outcomes (APOs) in women with gestational diabetes mellitus (GDM). Subjects and methods: This was a prospective, longitudinal and observational study conducted from April 2004 to November 200
Arch. Endocrinol. Metab.. Publicado em: 2019-01
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5. Effect of hydroxyurea (HU) on gelatinization mechanism of type I collagen suspensions
ABSTRACT Mutant hemoglobins thermodynamic phase transitions (HbS, HbC, etc.) have been the causes of serious hemoglobinopathies that have been affecting mankind since the dawn of human race. HbS polymerization is the best known of these transitions and the original cause of sickle cell anemia. Hydroxyurea (HU, NH2CONHOH) is widely used as the main drug admin
Matéria (Rio J.). Publicado em: 06/12/2018
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6. Clinical and laboratory profile of patients with sickle cell anemia
Abstract Objective: This study aimed to describe and analyze clinical and laboratory characteristics of patients with sickle cell anemia treated at the Hemominas Foundation, in Divinópolis, Brazil. Furthermore, this study aimed to compare the clinical and laboratory outcomes of the group of patients treated with hydroxyurea with those patients that were no
Rev. Bras. Hematol. Hemoter.. Publicado em: 2017-03
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7. Fetal hemoglobin and hemolysis markers in sickle cell anemia
Rev. Bras. Hematol. Hemoter.. Publicado em: 2015-06
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8. Pattern of hemolysis parameters and association with fetal hemoglobin in sickle cell anemia patients in steady state
Objective: This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomarkers in sickle cell anemia patients. Methods: Fifty adult sickle cell anemia patients were included in the study. All patients were taking hydroxyurea for at least six months and were followed at the outpatient clinic of a hospital in Fortaleza, Ceará, Braz
Rev. Bras. Hematol. Hemoter.. Publicado em: 2015-06
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9. Plasma levels and placental expression of vaspin in pregnant women with diabetes mellitus
The present study aimed to investigate visceral adipose tissue-specific serpin (vaspin) concentrations in serum and term placentas and relate these values to insulin resistance and lipid parameters in women with gestational diabetes mellitus (GDM). A total of 30 GDM subjects and 27 age-matched pregnant women with normal glucose tolerance (NGT, control) were
Braz J Med Biol Res. Publicado em: 20/01/2015
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10. Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia
Objectives: To analyze the frequency of βS-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia. Method: The frequency of βS-globin haplotypes and alpha-thalassemia and any association with clinical and laboratorial manifestations were determined in 117 si
Rev. Bras. Hematol. Hemoter.. Publicado em: 2014-10
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11. Influence of ?S-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia
Background: Sickle cell anemia is a chronic inflammatory disease characterized by an increased production of proinflammatory cytokines including tumor necrosis factor-alpha. Hydroxyurea, by decreasing the polymerization of hemoglobin, reduces inflammatory states. The effect of the genetic polymorphisms of sickle cell patients on tumor necrosis factor-alpha
Rev. Bras. Hematol. Hemoter.. Publicado em: 2014-04
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12. Análise de polimorfismos em genes envolvidos no estresse oxidativo e associação com a severidade da doença em pacientes com anemia falciforme = : Analysis of polymorphisms in genes involved in oxidative stress and association with the severity of the disease in patients with sickle cell disease / Analysis of polymorphisms in genes involved in oxidative stress and association with the severity of the disease in patients with sickle cell disease
Embora a anemia falciforme (AF) resulte da homozigosidade de uma única mutação, no codon 6 do locus da ?-globina, fenotipicamente, essa doença é muito heterogênea, de modo que diferentes pacientes podem apresentar evoluções clínicas significativamente distintas. As complicações nestes pacientes normalmente são decorrentes de acometimento vascular
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 21/08/2012