Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome von Deutsch, Samuel, Rideau, Alexandra, Bochaton-Piallat, Marie-Luce, Merla, Giuseppe, Geinoz, Antoine, Gabbiani, Giulio, Schwede, Torsten, Matthes, Thomas, Antonarakis, Stylianos E., Beris, Photis

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Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosis von Rideau, Alexandra, Mangeat, Bastien, Matthes, Thomas, Trono, Didier, Beris, Photis

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Molecular Mechanism of Hepcidin Deficiency in a Patient with Juvenile Hemochromatosis von Rideau, Alexandra, Mangeat, Bastien, Matthes, Thomas, Trono, Didier, Beris, Photis

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Development of a Model for the Study of PU.1 Function in Primary Human Hematopoietic Cells von Durual, Stephane, Rideau, Alexandra, Wiznerowics, Maciej, Ruault, Sylvie, Beris, Photis, Piguet, Vincent, Matthes, Thomas

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GATA-1 Overexpression Does Not Restore Deficient Erythropoiesis in Myelodysplastic Syndromes von Rideau, Alexandra, Durual, Stephane, Wiznerowics, Maciej, Ruault, Sylvie, Piguet, Vincent, Beris, Photis, Matthes, Thomas

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Case report: Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion von Matthes, Thomas, Rustin, Pierre, Trachsel, Hedwige, Darbellay, Regis, Costaridou, S, Xaidara, A, Rideau, Alexandra, Beris, Photis

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Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion von Matthes, Thomas, Rustin, Pierre, Trachsel, Hedwige, Darbellay, Régis, Costaridou, S., Xaidara, A., Rideau, Alexandra, Beris, Photis

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Aspl424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/fechtner syndrome von DEUTSCH, Samuel, RIDEAU, Alexandra, BOCHATON-PIALLAT, Marie-Luce, MERIA, Giuseppe, GEINOZ, Antoine, GABBIANI, Giulio, SCHWEDE, Torsten, MATTHES, Thomas, ANTONARAKIS, Stylianos E, BERIS, Photis

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Pathologie moléculaire de l'anémie sidéroblastique von KONDRAYEV, Alexander, RIDEAU, Alexandra, SAMII, Kaveh, MATTHES, Thomas, CABROL, Christine, KOVACSOVICS, Tibor, BERIS, Photis

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Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosis von Rideau, Alexandra, Mangeat, Bastien, Matthes, Thomas, Trono, Didier, Beris, Photis

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Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion von Matthes, Thomas, Rustin, Pierre, Trachsel, Hedwige, Darbellay, Régis, Costaridou, S., Xaidara, A., Rideau, Alexandra, Beris, Photis

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La poésie délivrée von Benini, Romain, Bobillot, Jean-Pierre, Bootz, Philippe, Boudon, Jacques-Olivier, Brissette, Pascal, Carinos, Emmanuelle, Cohen, Nadja, Darriulat, Philippe, Demartini, Anne-Emmanuelle, Denis, Benoît, Hammou, Karim, Héron, Pierre-Marie, Hirschi, Stéphane, Jalabert, Romain, Legoy, Corinne, Leterrier, Sophie-Anne, Linarès, Serge, Marchal, Hugues, Nachtergael, Magali, Nadaud, Éric, Pardo, Céline, Pillet, Élisabeth, Pistone, Pascal, Rideau, Gaël, Saemmer, Alexandra, Saint-Amand, Denis, Stead, Evanghélia, Suter, Patrick, Szendy, Peter, Vaillant, Alain, Vivès, Vincent, Vorger, Camille, Wisniewski, Marine, Zubiate, Jean-Pierre

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Varia von Audran, Karine, Belissa, Marc, Bergounioux, Paul, Bianchi, Serge, Chappey, Jean-Luc, Clay, Stephen, Crépin, Annie, Gainot, Bernard, Goujard, Philippe, Guilhaumou, Jacques, Halpern, Jean-Claude, Hyard, Alexandra, Monnier, Raymonde, Rideau, Gaël, Saunier, Éric, Weber, Jacques

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