Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia von Daoud, B. Ben, Mosbehi, I., Préhu, C., Chaouachi, D., Hafsia, R., Abbes, S.

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A New Silent β Chain Variant: Hb Hounslow [β80(EF4)Asn→Tyr] von Préhu, C, Riou, J, Henthorn, J, Wajcman, H

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Cation-exchange HPLC evaluated for presumptive identification of hemoglobin variants von Riou, Jean, Godart, Christian, Hurtrel, Didier, Mathis, Mireille, Bimet, Catherine, Bardakdjian-Michau, Josiane, Prehu, Claude, Wajcman, Henri, Galacteros, Frederic

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ABNORMAL HEMOGLOBINS: LABORATORY METHODS von Wajcman, Henri, Préhu, Claude, Bardakdjian-Michau, Josiane, Promé, Danielle, Riou, Jean, Godart, Christian, Mathis, Mireille, Hurtrel, Didier, Galactéros, Frederic

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Sickle Cell Anemia and β-Globin Gene Cluster Haplotypes in Colombia von Cuéllar-Ambrosi, F., Mondragón, M. C., Figueroa, M., Préhu, C., Galactéros, F., Ruiz-Linares, A.

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Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease von Lee, K., Préhu, C., Mérault, G., Kéclard, L., Roudot‐Thoraval, F., Bachir, D., Wajcman, H., Denis, L., Galactéros, F.

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

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Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia von Bendaoud, B., Hosni, I., Mosbahi, I., Hafsia, R., Prehu, C., Abbes, S.

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Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb antananarivo [α1(NA1)Val→Gly] and Hb barbizon [β144(HC1)Lys→Met] von Kister, J., Préhu, C., Riou, J., Godart, C., Bardakdjian, J., Promé, D., Galactéros, F., Wajcman, H.

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A study of 36 unrelated cases with pure erythrocytosis revealed three new mutations in the erythropoietin receptor gene von Al-Sheikh, Maha, Mazurier, Elodie, Gardie, Betty, Casadevall, Nicole, Galacteros, Frederic, Goossens, Michel, Wajcman, Henri, Prehu, Claude, Ugo, Valerie

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Hb Diamant [α119(H2)Pro→Leu]: A New Variant with a Modification at the α1β1 Interface von Préhu, C., Riou, J., Godart, C., Bost, M., Barro, C., Promé, D., Kister, J., Galactéros, F., Wajcman, H.

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Hemoglobin Phnom Penh [α117Phe(H1)-Ile-α118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the α1-globin gene von Wajcman, H., Préhu, M.O., Préhu, C., Blouquit, Y., Promé, D., Galactéros, F.

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Hb Nikaia [α20(Bl)His→Asp]: a New Variant of the α2 Gene von Préhu, C., Godart, C., Riou, J., Soummer, A. M., Promé, D., Galactéros, F., Wajcman, H.

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Two new α Chain variants found during glycated hemoglobin screening: HB Tatras [α7(A5)LYS→ASN] and HB Lisbon [aL23(B4)GLU→ASP] von Wajcman, H., Bost, M., Blouquit, Y., Préhu, C., Riou, J., Galacteros, F.

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Glucose-6-Phosphate Dehydrogenase Deficiency and Homozygous Sickle Cell Disease in Congo von Bouanga, Jean Claude, Mouélé, René, Préhu, Claude, Wajcman, Henri, Feingold, Josué, Galactéros, Frédéric

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A New Silent [beta] Chain Variant: Hb Hounslow [[beta]80(EF4)Asn->Tyr] von Préhu, C, Riou, J, Henthorn, J, Wajcman, H

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Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA von Wajcman, Henri, Lahary, Agnés, Promé, Danielle, Kister, Jean, Riou, Jean, Godart, Christian, Préhu, Claude, Traeger-Synodinos, Jan, Papassotiriou, Ioannis, Galactéros, Frederic

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Unexpected high frequency of P46L TNFRSF1A allele in sub-Saharan West African populations von TCHERNITCHKO, Dimitri, CHIMINQGI, Mihelaiti, GALACTEROS, Frédéric, PREHU, Claude, SEGBENA, Yvon, COULIBALY, Hamidou, REBAYA, Nadia, LORIC, Sylvain

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Les atteintes rénales, les ulcères cutanés et le priapisme sont associés à un pourcentage élevé de globules rouges denses au cours de la drépanocytose von Bartolucci, P., Brugnara, C., Teixeira-Pinto, A., Pissard, S., Moradkhani, K., Jouault, H., Prehu, C., Galacteros, F.

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