Authors: Corrons, JLV Besson, I

Citation: Jlv. Corrons et I. Besson, Red cell membrane Na+ transport systems in hereditary spherocytosis: relevance to understanding the increased Na+ permeability, ANN HEMATOL, 80(9), 2001, pp. 535-539

Authors: Corrons, JLV Pujades, A Alvarez, R Estella, J Dhermy, D

Citation: Jlv. Corrons et al., alpha I 28 Arg -> Ser (CGT -> AGT) spectrin mutation associated with severe neonatal elliptopoikilocytosis in Spain, HAEMATOLOG, 86(5), 2001, pp. 537-538

Authors: Corrons, JLV Alvarez, R Pujades, A Zarza, R Oliva, E Lasheras, G Callis, M Ribes, A Gelbart, T Beutler, E

Citation: Jlv. Corrons et al., Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinicaland molecular studies, BR J HAEM, 112(2), 2001, pp. 475-482

Authors: Pujades, A Lewis, M Salvati, AM Miwa, S Fujii, H Zarza, R Alvarez, R Rull, E Corrons, JLV

Citation: A. Pujades et al., Evaluation of the blue formazan spot test for screening glucose 6 phosphate dehydrogenase deficiency, INT J HEMAT, 69(4), 1999, pp. 234-236

Authors: Zarza, R Pujades, A Garcia, J Alvarez, R Carrera, A Estella, J Morey, M Remacha, A Perez-Lungmus, G Nomdedeu, B Sanchez, J Gastearena, J Bureo, E Corrons, JLV

Citation: R. Zarza et al., Molecular study of red cell pyruvate-kinase deficiency in 15 patients withchronic haemolytic anaemia, MED CLIN, 112(16), 1999, pp. 606-609