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Results: 1-8 |
Results: 8
Glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice
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
Homozygous glucose-6-phosphate dehydrogenase deficiency and propacetamol-induced hemolysis
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
A new case of hemoglobin Chesapeake
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
Neonatal screening of sickle cell disease in metropolitan France
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
Two new (G)gamma chain variants: Hb F-Clamart [gamma 17(A14)Lys -> Asn] and Hb F-Ouled Rabah [gamma 19(B1)Asn -> Lys]
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
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
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
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
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
Prevention of hereditary hemoglobin disorders.
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 |