Purification, amplification and characterization of a population of human erythroid progenitors von FREYSSINIER, J. M, LECOQ-LAFON, C, AMSELLEM, S, PICARD, F, DUCROCQ, R, MAYEUX, P, LACOMBE, C, FICHELSON, S

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Atypical sickle cell syndromes: A report on two cases von BOUZID, K, ODIEVRE, M.-H, ITHIER, G, BENKERROU, M, COUQUE, N, ELION, J, DUCROCQ, R

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Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease von Odievre, Marie-Helene, Bony, Viviane, Benkerrou, Malika, Lapoumeroulie, Claudine, Alberti, Corinne, Ducrocq, Rolande, Jacqz-Aigrain, Evelyne, Elion, Jacques, Cartron, Jean-Pierre

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Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease von DE MONTALEMBERT, M, BELLOY, M, MAIER-REDELSPERGER, M, ELION, J, LABIE, D, GIROT, R, BERNAUDIN, F, GOURAUD, F, CAPDEVILLE, R, MARDINI, R, PHILIPPE, N, JAIS, J. P, BARDAKDJIAN, J, DUCROCQ, R

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Neonatal screening for sickle cell disease in France von Bardakdjian-Michau, J, Bahuau, M, Hurtrel, D, Godart, C, Riou, J, Mathis, M, Goossens, M

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Strategy linking several analytical methods of neonatal screening for sickle cell disease von Ducrocq, R, Pascaud, O, Bévier, A, Finet, C, Benkerrou, M, Elion, J

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Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia von BADER-MEUNIER, Brigitte, VERLHAC, Suzanne, BARUCHEL, Andre, BENKERROU, Malika, ELMALEH-BERGES, Monique, ITHIER, Ghislaine, SELLAMI, Fatiha, FAID, Sonia, MISSUD, Florence, DUCROCQ, Rolande, ALBERTI, Corinne, ZACCARIA, Isabelle

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A novel sickle cell mutation by yet another origin in Africa : the Cameroon type von LAPOUMEROULIE, C, DUNDA, O, DUCROCQ, R, TRABUCHET, G, MONY-LOBE, M, BODO, J. M, CARNEVALE, P, LABIE, D, ELION, J, KRISHNAMOORTHY, R

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L’annonce du diagnostic de syndrome drépanocytaire majeur chez un nouveau-né von Niakaté, A., Cavazza, F., Perrin, A., Brousse, V., Bardakdjian, J., Ducrocq, R., de Montalembert, M.

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Molecular Basis of β-Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutation von JASSIM, N., MERGHOUB, T., PASCAUD, O., AL MUKHARRAQ, H., DUCROCQ, R., LABIE, D., ELION, J., KRISHNAMOORTHY, R., AL ARRAYED, S.

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The role of the G6PD A-376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the Seerer population of Senegal von DE ARAUJO, Caria, MIGOT-NABIAS, Florence, GUITARD, Juliette, PELLEAU, Stéphane, VULLIAMY, Tom, DUCROCA, Rolande

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Announcing the diagnosis of sickle cell disease in a newborn to the parents von Niakaté, A, Cavazza, F, Perrin, A, Brousse, V, Bardakdjian, J, Ducrocq, R, de Montalembert, M

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Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea von Lapoumeroulie, C, Benkerrou, M, Odievre, MH, Ducrocq, R, Brun, M, Elion, J

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Historique de l'implantation des pharmacies mutualistes en Seine-Maritime: le point de vue d'un pharmacien d'officine von DUCROCQ, R

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Perfusion Chromatography Allows an Order of Magnitude Faster Measurement of the Gγ:Aγ Ratio in Patients With an Increased Level of Fetal Hemoglobin von Wajcman, H., Galacteros, F., Ducrocq, R.

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Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals von Merghoub, T, Maier-Redelsperger, M, Labie, D, Perichon, B, Feingold, N, Dibenedetto, S P, Schiliro, G, Samperi, P, Ducrocq, R, Elion, J, Krishnamoorthy, R

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Gamma Chain Heterogeneity: Determination of Hb F Composition by Perfusion Chromatography von Papassotiriou, I., Ducrocq, R., Préhu, C., Bardakdjian-Michau, J., Wajcman, H.

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Acute clinical events in 299 homozygous sickle cell patients living in France von Neonato, Maria Grazia, Guilloud-Bataille, Monique, Beauvais, Pierre, Bégué, Pierre, Belloy, Marie, Benkerrou, Malika, Ducrocq, Rolande, Maier-Redelsperger, Micheline, De Montalembert, Mariane, Quinet, Béatrice, Elion, Jacques, Feingold, Josué, Girot, Robert

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Determination of Hb F Levels: The Routine Methods von Préhu, C., Ducrocq, R., Godart, C., Riou, J., Galactéros, F.

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Compound heterozygosity Hb S/Hb Hope (β136Gly→Asp): a pitfall in the newborn screening for sickle cell disease von Ducrocq, R, Bévier, A, Leneveu, A, Maier-Redelsperger, M, Bardakdjian-Michau, J, Badens, C, Elion, J

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