Results 111 to 120 of about 36,976 (279)
Heterozygous Beta-Thalassemia in Association with Hereditary Elliptocytosis: A Family Study [PDF]
, 1965 Pasquale E. Perillie, Amoz I. Chernoff
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Plastic bronchitis in beta thalassemia minor
Lung India, 2013 Plastic bronchitis is a rare pulmonary disorder associated with various conditions like cystic fibrosis, asthma, pulmonary infection and characterized by formation and expectoration of cast which assumes the shape of the bronchial tree. We report a case of a 33-year-old woman with beta thalassemia minor who developed plastic bronchitis.
Jyotsna M Joshi +2 more
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Absence of beta mRNA in beta0-thalassemia in Kurdish Jews [PDF]
, 1978 Francesco Ramirez +5 more
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The compound state: Hb S/beta-thalassemia
Revista Brasileira de Hematologia e Hemoterapia, 2015 The polymerization of deoxygenated Hb S (sickling) is theprimary event in the molecular pathogenesis of SCD. How-ever, this event is highly dependent on the intracellular Hbcomposition; in other words, it is dependent on the concen-tration of Hb S, and type and concentration of the other typesof Hb.
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An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta- thalassemia [PDF]
, 1987 JC Diaz-Chico +5 more
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The levels of nitric oxide in beta-thalassemia minor
Turkish Journal of Hematology, 2008 OBJECTIVE: The aim of this study was to investigate the relationship between NO (nitric oxide) and beta-thalassemia minor. METHODS: A total of 60 patients with beta-thalassemia minor (30 M, 30 F) were included in the study. The control group consisted of
Yalçın Başaran +3 more
doaj
Pulmonary hypertension in adolescents with sickle cell disease [PDF]
, 2016 Sickle cell disease consists of a group of disorders that have a similar mutation in at least one of the beta-globin chains of hemoglobin. This results in a change of the hemoglobin to sickle shaped cells when in the deoxygenated state.
Akinyemi, Katherine
core +1 more source
beta 0 thalassemia, a nonsense mutation in man. [PDF]
, 1979 Judy C. Chang, Y Kan
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Beta-thalassemia: from genotype to phenotype
Haematologica, 2011 Beta-thalassemias are heterogeneous autosomal recessive hereditary anemias characterized by reduced or absent β globin chain synthesis. The resulting relative excess of unbound α globin chains precipitate in erythroid precursors in the bone marrow, leading to their premature death and, hence ...
DANJOU, FABRICE +2 more
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Lipid membrane peroxidation in beta-thalassemia major [PDF]
, 1976 EA Rachmilewitz, SB Shohet, BH Lubin
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