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Increased susceptibility of microcytic red blood cells to in vitro oxidative stress
Abstract: Oxidative damage to erythrocytes in thalassaemia has been related to generation of free radicals by an excess of denaturated α‐ or β‐globin chains, intracellular iron overload and lowExpand
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Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
delta beta-Thalassemia and hereditary persistence of fetal hemoglobin (HPFH) are inherited disorders characterized by the persistent synthesis of fetal hemoglobin (HbF) during adult life. The SpanishExpand
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Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
delta beta-Thalassemia and hereditary persistence of fetal hemoglobin (HPFH) are inherited disorders characterized by the persistent synthesis of fetal hemoglobin (HbF) during adult life. The SpanishExpand
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