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- Publications
- Influence
Increased susceptibility of microcytic red blood cells to in vitro oxidative stress
- J. L. Vives Corrons, A. Miguel-García, +5 authors M. A. Calvo
- Biology, Medicine
- European journal of haematology
- 1 November 1995
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 low… Expand
Rapid Detection of Spanish ( S @ ) O-Thalassemia Deletion by Polymerase Chain Reaction
- By J. L. Vives-Corrons, M. Pujades, A. Miguel-García, A. MigueCSosa, S. Cambiazzo
- 6
- 1
Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
- J. L. Vives-corrons, M. Pujades, A. Miguel-García, A. Miguel-Sosa, S. Cambiazzo
- Medicine
- Blood
- 1992
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 Spanish… Expand
Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
- Jl Vives-Corrons, MA Pujades, A. Miguel-García, A. Miguel-Sosa, S. Cambiazzo
- Biology
- 15 September 1992
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 Spanish… Expand