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:
Bardakjian, J
Benkerrou, M
Bernaudin, F
Briard, ML
Ducrocq, R
Lambilliotte, A
Lena-Russo, D
de Montalembert, M
Thuret, I
Begue, P
Elion, J
Galacteros, F
Citation: J. Bardakjian et al., Neonatal screening of sickle cell disease in metropolitan France, ARCH PED, 7(12), 2000, pp. 1261-1263
Authors:
Wajcman, H
Borensztajn, K
Riou, J
Prome, D
Hurtrel, D
Bardakdjian, J
Lena-Russo, D
Amouroux, I
Ducrocq, R
Citation: H. Wajcman et al., Two new (G)gamma chain variants: Hb F-Clamart [gamma 17(A14)Lys -> Asn] and Hb F-Ouled Rabah [gamma 19(B1)Asn -> Lys], HEMOGLOBIN, 24(1), 2000, pp. 45-52
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