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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Precision of CAPILLARYS 2 for the Detection of Hemoglobin Variants Based on Their Migration Positions von Riou, Jean, Szuberski, Jessica, Godart, Christian, Wajcman, Henri, Oliveira, Jennifer L, Hoyer, James D, Bardakdjian-Michau, Josiane

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A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an α2 globin gene variant (Hb Conakry) von Cohen‐Solal, Michel, Préhu, Claude, Wajcman, Henri, Poyart, Claude, Bardakdjian‐Michau, Josiane, Kister, Jean, Promé, Danielle, Valentin, Colette, BAchir, Dora, Galactéros, Frédéric

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Hemoglobins in Togolese Newborns: Hb S, Hb C, Hb Bart's, and α‐Globin Gene Status von Segbena, Akueté Yvon, Prehu, Claude, Wajcman, Henri, Bardakdjian‐Michau, Josiane, Messie, Kodjovi, Feteke, Lochina, Vovor, Anne, David, Mireille, Feingold, Josué, Galacteros, Frédéric

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Two New Hemoglobin Variants with Increased Oxygen Affinity: Hb Nantes [β34(B16)Val → Leu] and Hb Vexin [β116(G18)His → Leu] von Wajcman, Henri, Bardakdjian-Michau, Josiane, Riou, Jean, Préhu, Claude, Kister, Jean, Baudin-Creuza, Véronique, Promé, Danielle, Richelme-David, Suzy, Luc Harousseau, Jean, Galactéros, Frédéric

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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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Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD von Trudel, M., Saadane, N., Garel, M.C., Bardakdjian‐Michau, J., Blouquit, Y., Guerquin‐Kern, J.L., Rouyer‐Fessard, P., Vidaud, D., Pachnis, A., Roméo, P.H.

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DECREASED MORBIDITY IN HOMOZYGOUS SICKLE CELL DISEASE DETECTED AT BIRTH von Bardakdjian-Michau, Josiane, Guilloud-Bataille, Monique, Maier-Redelsperger, Micheline, Elion, Jacques, Girot, Robert, Feingold, Josué, Galactéros, Frédéric, Montalembert, Mariane de

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Le dépistage néonatal de la drépanocytose en France: Drépanocytose von BARDAKDJIAN-MICHAU, Josiane

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Haemoglobin J‐Biskra: a new mildly unstable α1 gene variant with a deletion of eight residues (α50–57, α51–58 or α52–59) including the distal histidine von Wajcman, Henri, Dahmane, Malika, Préhu, Claude, Costes, Bruno, Promé, Danielle, Arous, Nicole, Bardakdjian‐Michau, Josiane, Riou, Jean, Ayache, Kadour Cherif, Godart, Christian, Galactéros, Frédéric

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Hb TSUKUMI [β117(G19)His →Tyr] FOUND IN A MOROCCAN WOMAN von North, Marie L., Duwig, Isabelle, Riou, Jean, Promé, Danielle, Yapo, Angué P., Kister, Jean, Bardakdjian-Michau, Josiane, Cazenave, Jean P., Wajcman, Henri

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Sickle Cell Disease in a Patient with Sickle Cell Trait and Compound Heterozygosity for Hemoglobin S and Hemoglobin Quebec–Chori von Witkowska, H. Ewa, Lubin, Bertram H, Beuzard, Yves, Baruchel, Sylvain, Esseltine, Dixie W, Vichinsky, Elliott P, Kleman, Klara M, Bardakdjian-Michau, Josiane, Pinkoski, Linda, Cahn, Sarah, Roitman, Esther, Green, Brian N, Falick, Arnold M, Shackleton, Cedric H.L

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A NEW Gγ CHAIN VARIANT: Hb F-COIGNIERES [γ75(E19)Ile → Val] von Wajcman, Henri, Yapo, Angoué P., Riou, Jean, Promé, Danielle, Richelme-David, Suzy, Hurtrel, Didier, Bardakdjian-Michau, Josiane

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Brief Report: Sickle Cell Disease in a Patient with Sickle Cell Trait and Compound Heterozygosity for Hemoglobin S and Hemoglobin Quebec-Chori von Witkowska, H Ewa, Lubin, Bertram H, Beuzard, Yves, Baruchel, Sylvain, Esseltine, Dixie W, Vichinsky, Elliott P, Kleman, Klara M, Bardakdjian-Michau, Josiane, Pinkoski, Linda, Cahn, Sarah, Roitman, Esther, Green, Brian N, Falick, Arnold M, Shackleton, Cedric HL

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Le dépistage néonatal ciblé de la drépanocytose en France métropolitaine : raisons et résultats von BENKERROU, Malika

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