Beta-thalassemia
![Hb C [beta6(A3)Glu>Lys] and IVS II - 654 (C>T) beta thalassemia interaction in Brazil.](data:image/gif;base64,R0lGODlhAQABAIAAAP///wAAACH5BAEAAAAALAAAAAABAAEAAAICRAEAOw==)
Hb C [beta6(A3)Glu>Lys] and IVS II - 654 (C>T) beta thalassemia interaction in Brazil.
... Thalassemias are a heterogeneous group of inherited disorders characterized by a microcytic hypochromic anemia and an imbalancein thesynthesisof theglobin- chains. Hb C is the second most frequently variant of hemoglobin ...
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HAEMOGLOBIN E/ BETA - THALASSEMIA: A CASE REPORT FROM UPPER ASSAM, INDIA
... INTRODUCTION: Hb E/beta-thalassemia (E/β thalassemia) is the commonest form of severe thalassemia in many Asian countries. It has become an increasingly severe public health problem in upper ...
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Repositório Institucional da UFPA: Oxidative stress and antioxidant status in beta-thalassemia heterozygotes
... of thalassemia mutations on the TBARS and TEAC values, samples were subdivided according to ...for beta-thalassemia, 18 (37%) carried the CD39 mutation, 23 (47%) carried the IVS-I-110 mutation, one ...
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The profile of beta thalassemia obtained by data mining analysis in a database.
... heterozygous beta thalassemia reflect the formation of different ...heterozygous beta-thalassemia of the Brazilian population, we aimed at establishing parameters to direct the diagnosis of ...
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Serum ferritin levels in beta thalassemia carrier.
... de beta talassemia foi baseado em hemo- grama (Pentras 120 Retic-Horiba ABX), na quantificação das Hb A2 e Hb Fetal por HPLC (Bio-Rad) e na análise morfo- lógica de sangue ...
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Rev. Bras. Hematol. Hemoter. vol.38 número4
... with beta-thalassemia major includes chronic transfusion therapy, iron chelation, splenec- tomy, allogeneic hematopoietic stem cell transplantation and support ...
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J. Bras. Patol. Med. Lab. vol.53 número6
... Introduction: Beta-thalassemia is caused by a deicient synthesis of the ß-chain of hemoglobin, which leads to a chronic, microcytic and hypochromic ...of thalassemia, and their frequencies may vary ...
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Rev. Bras. Hematol. Hemoter. vol.34 número6
... S/Beta thalassemia adults who had taken HU for 2 to 3 ...S/Beta thalassemia due to microcytosis and hypochromia of the thalassemic cell population, which varies according to the beta ...
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Rev. Bras. Hematol. Hemoter. vol.30 número4
... Immigrants from many parts of the world settled in Paraná State in Brazil, contributing to the diversified genetic patrimony of its population. This characteristic led us to investigate, for the first time, the incidence ...
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Thalassemia screening in Brazil: results for 20 years
... Thalassemic syndromes more frequently affect people in the southern and southeastern regions, especially because of the racial characteristics of these populations. Many hemoglobin variants have been described in Brazil, ...
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Rev. Bras. Hematol. Hemoter. vol.33 número6
... The XmnI polymorphism was observed in 36.5% of heterozygous beta-thalassemia patients and in 41.4% of control subjects. There was no statistically significant difference between the two groups (p-value = ...
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Rev. Bras. Hematol. Hemoter. vol.35 número6
... 2. Livrea MA, Tesoriere L, Pintaudi AM, Calabrese A, Maggio A, Freisleben HJ, et al. Oxidative stress and antioxidant status in beta-thalassemia major: iron overload and depletion of lipid-soluble ...
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Rev. Bras. Hematol. Hemoter. vol.35 número6
... in beta-thalassemia carriers compared with the control group (independent t-test; p-value < ...for beta-thalassemia had TBARS values above the reference ...
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Sao Paulo Med. J. vol.130 número4
... Six out of the 30 patients were clinically symptomatic and pre- sented anemia, jaundice, pallor and weaknesses. The patients’ peripheral smears showed microcytic hypochromic red cells with few target cells. A mild degree ...
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Rev. Bras. Hematol. Hemoter. vol.39 número2
... and beta-thalassemia minor adults, but no significant dif- ference was observed in the thiobarbituric acid reactive species levels and FoxO3 gene expression (p-value ...of beta-thalassemia ...
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Rev. Bras. Hematol. Hemoter. vol.37 número3
... 10. Boletini E, Svobodova M, Divoky V, Baysal E, Curuk MA, Dimovski AJ, et al. Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations. Hum ...
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Uma nova classe de distribuições generalizadas.
... , (3.2) sendo que x > 0, a > 0, b > 0, σ > 0, −∞ < c < +∞, −∞ < µ < +∞, φ(·) é a fdp normal padrão e Φ(·) é fd normal padrão. Caso, c = 0, tem-se o modelo beta log-normal, para a = b = 1 e ...
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Arq. Bras. Cardiol. vol.94 número6
... The beta-blockers appeared as a great advance in cardiology for the treatment of HF; however, the drug response varies according to each patient, as several factors are associated, such as the genetic ...
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Eletrencefalograma quantitativo e topográfico (mapeamento cerebral): estudo do padrão normal para uma população adulta.
... atividade beta em: beta frontal, que é muito comum, muito rápida, sem relação com outros ritmos fisiológicos; beta central, que pode se originar do ritmo “mu”, aparecendo misturada a ele; beta ...
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EXTENDED-SPECTRUM BETA-LACTAMASE PRODUCTION AMONG AMPICILLIN-RESISTANT ESCHERICHIA COLI STRAINS FROM CHICKEN IN ENUGU STATE, NIGERIA Chah, K.F.1 ; Oboegbulem, S.I.2
... In the present study a greater proportion of the ESBL- producers were detected with cefotaxime alone versus cefotaxime/clavulanate discs than with ceftazidime versus ceftazidime/clavulanate discs. This finding is ...
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