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Results: 1-8 |
Results: 8

Authors: Badens, C Leclaire, M Collomb, J Auquier, P Soyer, P Michel, G Mattei, JF Lena-Russo, D
Citation: C. Badens et al., Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice, PRESSE MED, 30(11), 2001, pp. 524-526

Authors: Oliver, M Coton, T Badens, C Dehan, C Lena-Russo, D Moalic, JL
Citation: M. Oliver et al., Homozygous glucose-6-phosphate dehydrogenase deficiency and propacetamol-induced hemolysis, HAEMATOLOG, 86(9), 2001, pp. 987-988

Authors: Granel, B Serratrice, J Badens, C Lena-Russo, D Disdier, P Weiller, PJ
Citation: B. Granel et al., A new case of hemoglobin Chesapeake, HAEMATOLOG, 86(1), 2001, pp. 105-105

Authors: Badens, C
Citation: C. Badens, Prevention of hemoglobinopathies in non-endemic countries., B S PATH EX, 94(2), 2001, pp. 98-100

Authors: Aguilar-Martinez, P Schved, JF Badens, C Thuret, I Michel, G Neonato, MG Peltier, JY Girot, R Pissard, S Galacteros, F Bachir, D Rose, C Picot, MC Denamur, E Elion, J
Citation: P. Aguilar-martinez et al., Iron overload in thalassaemias and genetic haemochromatosis, EUR J HAEMA, 64(4), 2000, pp. 279-280

Authors: Badens, C Jassim, N Martini, N Mattei, JF Elion, J Lena-Russo, D
Citation: C. Badens et al., Characterization of a new polymorphism, IVS-I-108 (T -> C), and a new beta-thalassemia mutation,-27 (A -> T), discovered in the course of a prenatal diagnosis, HEMOGLOBIN, 23(4), 1999, pp. 339-344

Authors: Badens, C Lena-Russo, D Lacan, P Francina, A Prome, D Riou, J Geoffroy, M Ayavou, T Kister, J Galacteros, F Wajcman, H
Citation: C. Badens et al., Hb Toulon [alpha 77(EF6)Pro -> His]: a new variant due to a mutation in the alpha 2 gene found during measurement of glycated hemoglobin, HEMOGLOBIN, 23(4), 1999, pp. 367-371

Authors: Badens, C Mattei, JF Lena-Russo, D
Citation: C. Badens et al., Prevention of hereditary hemoglobin disorders., ANN PEDIAT, 46(1), 1999, pp. 8-14
Risultati: 1-8 |