Thalassemia
Mostrando 13-24 de 330 artigos, teses e dissertações.
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13. Immobile Tricuspid Valve: Incidental Finding in a Case of Terminal Cardiomyopathy Due to Thalassemia Major
Arq. Bras. Cardiol.. Publicado em: 10/10/2019
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14. Prevalência de hemoglobinopatias na população adulta brasileira: Pesquisa Nacional de Saúde 2014-2015
RESUMO: Objetivo: Descrever a prevalência das hemoglobinopatias da população adulta brasileira, segundo exames laboratoriais da Pesquisa Nacional de Saúde. Métodos: Estudo descritivo realizado com os dados laboratoriais da Pesquisa Nacional de Saúde coletados entre os anos de 2014 e 2015. A pesquisa de hemoglobinopatias foi feita pelo método da cr
Rev. bras. epidemiol.. Publicado em: 07/10/2019
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15. Characterization of thalassemia major and diabetes mellitus patients at a reference center in Brazil
ABSTRACT Objective: This is a quantitative transversal study that aimed to analyze the sociodemographic and clinical characteristics of thalassemia major patients with and without diabetes mellitus. Method: The cohort consisted of 31 thalassemia major patients from a reference center of treatment in Brazil in 2016. The data were obtained from an interview
Hematol., Transfus. Cell Ther.. Publicado em: 10/06/2019
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16. Echocardiografic abnormalities in patients with sickle cell/β-thalassemia do not depend on the β-thalassemia phenotype
ABSTRACT Objectives and methods: We evaluated possible relationships between echocardiographic findings and clinical and laboratory parameters, in a cohort of Brazilian patients diagnosed with sickle cell/β-thalassemia, to better understand the cardiac involvement in this disease. Results: Left atrial (LA) and left ventricular (LV) dilation were found in
Hematol., Transfus. Cell Ther.. Publicado em: 10/06/2019
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17. Hepatitis E virus prevalence in Egyptian children with transfusion-dependent thalassemia
ABSTRACT Hepatitis E virus (HEV) infection is one of the major public health problems in developing countries. HEV can cause chronic infections in immunocompromised individuals e.g. thalassemic patients with increased risk of morbidity and mortality. In addition there is possibility of HEV transmission through blood transfusion. Therefore, the present study
Braz J Infect Dis. Publicado em: 20/05/2019
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18. Intraocular pressure in subjects with beta-thalassemia minor
RESUMO Objetivo: Beta-talassemia menor é uma doença hereditária comum no sangue em países mediterrâneos como a Turquia e está associada à resistência à insulina. A resistência à insulina por sua vez, pode estar associada à pressão intraocular excessivamente alta e, portanto à cegueira induzida pela pressão intraocular. Este estudo teve como o
Arq. Bras. Oftalmol.. Publicado em: 25/02/2019
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19. Prevalence of anemia in schools of the metropolitan region of Curitiba, Brazil
ABSTRACT Background: Anemia during childhood is one of the biggest public health problems worldwide, including Brazil. Insufficient or abnormal production of hemoglobin, loss of iron and excessive destruction of red blood cells are the most common causes of anemia. Among the reasons of anemia, iron deficiency accounts for 50% of anemia cases in developing c
Hematol., Transfus. Cell Ther.. Publicado em: 2018-06
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20. Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease
ABSTRACT Cerebrovascular disease, particularly stroke, is one of the most severe clinical complications associated with sickle cell disease and is a significant cause of morbidity in both children and adults. Over the past two decades, considerable advances have been made in the understanding of its natural history and enabled early identification and treatm
Hematol., Transfus. Cell Ther.. Publicado em: 2018-06
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21. Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India
Hematol., Transfus. Cell Ther.. Publicado em: 2018-03
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22. Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients
Abstract Alpha-thalassemias are among the most common genetic diseases in the world. They are characterized by hypochromic and microcytic anemia and great clinical variability, ranging from a practically asymptomatic phenotype to severe anemia, which can lead to intrauterine or early neonatal death. Deletions affecting the α-globin genes, located on chromos
Genet. Mol. Biol.. Publicado em: 02/10/2017
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23. Assessment of the Matos & Carvalho index for distinguishing thalassemia from iron deficiency anemia
Rev. Bras. Hematol. Hemoter.. Publicado em: 2017-09
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24. Foxo3 gene expression and oxidative status in beta-thalassemia minor subjects
ABSTRACT Background: Oxidative stress may aggravate symptoms of hemolytic anemias such as beta-thalassemia. FoxO3 activation results in resistance to oxidative stress in fibroblasts and neuronal cell cultures. Objective: The purpose of this research was to study FoxO3 gene expression and oxidative status in beta-thalassemia minor individuals. Methods: Six
Rev. Bras. Hematol. Hemoter.. Publicado em: 2017-06