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Oxidative stress and antioxidant status in beta-thalassemia heterozygotes
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2013)
Background:Several studies have evaluated the oxidant and antioxidant status of thalassemia patients but most focused mainly on the severe and intermediate states of the disease. Moreover, the oxidative status has not been ...
Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population
(2011-11-16)
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has reduced expression in adults, ranging from 0 to 1% of total hemoglobin. Increased levels of Hb F are due to mutations in ...
Influence of δβ-thalassemia or regulatory elements in individuals with increased fetal Hb levels in the São Paulo northwest population
(2011-11-16)
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has reduced expression in adults, ranging from 0 to 1% of total hemoglobin. Increased levels of Hb F are due to mutations in ...
Genetic analysis of beta-thalassemia major and beta-thalassemia intermedia in Brazil
(Marcel Dekker IncNew YorkEUA, 1998)
Hemoglobin Interlaken in combination with beta thalassemia trait
(PAGEPress®, 2013-01)
We report a rare a1 globin gene variant (Hb Interlaken) found in a 63-year-old woman of Italian ancestry living in Buenos Aires Province, Argentina. The variant, a missense mutation at cd15 (GGT → GAT) causing a Gly →Asp ...
Measurement of reticulocyte and red blood cell indices in patients with iron deficiency anemia and beta-thalassemia minor
(Walter De Gruyter & CoBerlinAlemanha, 2005)