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Results: 1-16 |
Results: 16
Hb Douala [alpha 3(A1)Ser -> Phe]: A new alpha 1 gene mutation in a Cameroonian woman heterozygous for Hb S and a 3.7 kb deletional alpha-thalassemia
Authors: Prehu, C Hanichi, A Yapo, AP Claparols, C Prome, D Riou, J Wajcman, H
Citation: C. Prehu et al., Hb Douala [alpha 3(A1)Ser -> Phe]: A new alpha 1 gene mutation in a Cameroonian woman heterozygous for Hb S and a 3.7 kb deletional alpha-thalassemia, HEMOGLOBIN, 25(3), 2001, pp. 323-329
Abnormal hemoglobins: Laboratory methods
Authors: Wajcman, H Prehu, C Bardakdjian-Michau, J Prome, D Riou, J Godart, C Mathis, M Hurtrel, D Galacteros, F
Citation: H. Wajcman et al., Abnormal hemoglobins: Laboratory methods, HEMOGLOBIN, 25(2), 2001, pp. 169-181
Hb Mont Saint Aignan [beta 128(H6)Ala -> Pro]: A new unstable variant leading to chronic microcytic anemia
Authors: Wajcman, H Lahary, A Prome, D Kister, J Riou, J Godart, C Prehu, C Traeger-Synodinos, J Papassotiriou, I Galacteros, F
Citation: H. Wajcman et al., Hb Mont Saint Aignan [beta 128(H6)Ala -> Pro]: A new unstable variant leading to chronic microcytic anemia, HEMOGLOBIN, 25(1), 2001, pp. 57-65
HbF in the adult: could its composition discriminate normal from abnormal foetal globin gene expression?
Authors: Wajcman, H Galacteros, F Hanichi, A Yapo, A Prehu, C
Citation: H. Wajcman et al., HbF in the adult: could its composition discriminate normal from abnormal foetal globin gene expression?, CR AC S III, 323(11), 2000, pp. 975-981
Hb nikaia [alpha 20(B1)His -> Asp]: A new variant of the alpha 2 gene
Authors: Prehu, C Godart, C Riou, J Soummer, AM Prome, D Galacteros, F Wajcman, H
Citation: C. Prehu et al., Hb nikaia [alpha 20(B1)His -> Asp]: A new variant of the alpha 2 gene, HEMOGLOBIN, 24(4), 2000, pp. 305-309
Sickle cell anemia and beta-globin gene cluster haplotypes in Colombia
Authors: Cuellar-Ambrosi, F Mondragon, MC Figueroa, M Prehu, C Galacteros, F Ruiz-Linares, A
Citation: F. Cuellar-ambrosi et al., Sickle cell anemia and beta-globin gene cluster haplotypes in Colombia, HEMOGLOBIN, 24(3), 2000, pp. 221-225
Hb diamant [alpha 119(H2)Pro -> Leu]: a new variant with a modification atthe alpha 1 beta 1 interface
Authors: Prehu, C Riou, J Godart, C Bost, M Barro, C Prome, D Kistel, J Galacteros, F Wajcman, H
Citation: C. Prehu et al., Hb diamant [alpha 119(H2)Pro -> Leu]: a new variant with a modification atthe alpha 1 beta 1 interface, HEMOGLOBIN, 24(3), 2000, pp. 249-252
Two new variants with the same substitution at position beta 122: Hb Bushey [beta 122(GH5)Phe -> Leu] and Hb Casablanca [beta 65(E9)Lys -> Met;beta 122(GH5)Phe -> Leu]
Authors: Wajcman, H Drupt, F Henthorn, JS Kister, J Prehu, C Riou, J Prome, D Galacteros, F
Citation: H. Wajcman et al., Two new variants with the same substitution at position beta 122: Hb Bushey [beta 122(GH5)Phe -> Leu] and Hb Casablanca [beta 65(E9)Lys -> Met;beta 122(GH5)Phe -> Leu], HEMOGLOBIN, 24(2), 2000, pp. 125-132
Molecular genetics of glucose-6-phosphate dehydrogenase deficiency in a population of newborns from Ivory Coast
Authors: Coulibaly, FH Koffi, G Toure, HA Bouanga, JC Allangba, O Tolo, A Sawadogo, D Sanogo, I Konate, S Prehu, C Sangare, A Galacteros, F
Citation: Fh. Coulibaly et al., Molecular genetics of glucose-6-phosphate dehydrogenase deficiency in a population of newborns from Ivory Coast, CLIN BIOCH, 33(5), 2000, pp. 411-413
Hb Roubaix [alpha 55(E4)Val -> Leu]: a new neutral hemoglobin variant involving the alpha 1 gene
Authors: Prehu, C Bost, M Barro, C Prome, D Riou, J Godart, C Kister, J Galacteros, F Wajcman, H
Citation: C. Prehu et al., Hb Roubaix [alpha 55(E4)Val -> Leu]: a new neutral hemoglobin variant involving the alpha 1 gene, HEMOGLOBIN, 23(4), 1999, pp. 361-365
Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb antananarivo [alpha 1(NA1)Val -> Gly] and Hb Barbizon [beta 144(HCl)Lys -> Met]
Authors: Kister, J Prehu, C Riou, J Godart, C Bardakdjian, J Prome, D Galacteros, F Wajcman, H
Citation: J. Kister et al., Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb antananarivo [alpha 1(NA1)Val -> Gly] and Hb Barbizon [beta 144(HCl)Lys -> Met], HEMOGLOBIN, 23(1), 1999, pp. 21-32
Genetic and hematological studies in a group of 114 adult patients with SCsickle cell disease (vol 59, pg 15, 1998)
Authors: Lee, K Prehu, C Merault, G Keclard, L Roudot-Thoraval, F Bachir, D Wajcman, H Denis, L Galacteros, F
Citation: K. Lee et al., Genetic and hematological studies in a group of 114 adult patients with SCsickle cell disease (vol 59, pg 15, 1998), AM J HEMAT, 62(2), 1999, pp. 126-126
Determination of Hb F levels: The routine methods
Authors: Prehu, C Ducrocq, R Godart, C Riou, J Galacteros, F
Citation: C. Prehu et al., Determination of Hb F levels: The routine methods, HEMOGLOBIN, 22(5-6), 1998, pp. 459-467
Gamma chain heterogeneity: Determination of Hb F composition by perfusion chromatography
Authors: Papassotiriou, I Ducrocq, R Prehu, C Bardakdjian-Michau, J Wajcman, H
Citation: I. Papassotiriou et al., Gamma chain heterogeneity: Determination of Hb F composition by perfusion chromatography, HEMOGLOBIN, 22(5-6), 1998, pp. 469-481
Hb Tende [beta 124(H2)Pro -> Leu]: A new variant with a moderate increase in oxygen affinity
Authors: Wajcman, H Kister, J Prehu, C Riou, J Godart, C Bardakdjian, J Soummer, AM Prome, D Galacteros, F
Citation: H. Wajcman et al., Hb Tende [beta 124(H2)Pro -> Leu]: A new variant with a moderate increase in oxygen affinity, HEMOGLOBIN, 22(5-6), 1998, pp. 517-523
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha 2 globin gene variant (Hb Conakry)
Authors: Cohen-Solal, M Prehu, C Wajcman, H Poyart, C Bardakdjian-Michau, J Kister, J Prome, D Valentin, C Bachir, D Galacteros, F
Citation: M. Cohen-solal et al., A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha 2 globin gene variant (Hb Conakry), BR J HAEM, 103(4), 1998, pp. 950-956
Risultati: 1-16 |