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:
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