Search Results - LE MOËL, Gisèle

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  1. 1
    Proposal for a new set of classification criteria for adult-onset still disease

    Proposal for a new set of classification criteria for adult-onset still disease by Fautrel, Bruno, Zing, Emmanuel, Golmard, Jean-Louis, Le Moel, Giselle, Bissery, Anne, Rioux, Christophe, Rozenberg, Sylvie, Piette, Jean-Charles, Bourgeois, Pierre

    Published in Medicine (Baltimore)
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  2. 2
    Hypovitaminosis C in hospitalized patients

    Hypovitaminosis C in hospitalized patients by Fain, Olivier, Pariés, Jacques, Jacquart, Benoı̂t, Le Moël, Giséle, Kettaneh, Adrien, Stirnemann, Jérôme, Héron, Célia, Sitbon, Muriel, Taleb, Chérifa, Letellier, Edouard, Bétari, Bouchra, Gattegno, Liliane, Thomas, Michel

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  3. 3
    Percentage of glycosylated serum ferritin remains low throughout the course of adult onset Still's disease

    Percentage of glycosylated serum ferritin remains low throughout the course of adult onset Still's disease by Vignes, Stéphane, Le Moël, Gisèle, Fautrel, Bruno, Wechsler, Bertrand, Godeau, Pierre, Piette, Jean-Charles

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  4. 4
    Diagnostic value of ferritin and glycosylated ferritin in adult onset Still's disease

    Diagnostic value of ferritin and glycosylated ferritin in adult onset Still's disease by FAUTREL, Bruno, LE MOËL, Gisèle, BOURGEOIS, Pierre, SAINT-MARCOUX, Bernadette, TAUPIN, Pierre, VIGNES, Stéphane, ROZENBERG, Sylvie, KOEGER, Anne-Claude, MEYER, Olivier, GUILLEVIN, Loïc, PIETTE, Jean-Charles

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  5. 5
    High ferritin and low glycosylated ferritin may also be a marker of excessive macrophage activation

    High ferritin and low glycosylated ferritin may also be a marker of excessive macrophage activation by LAMBOTTE, Olivier, CACOUB, Patrice, COSTEDOAT, Nathalie, LE MOEL, Gisele, AMOURA, Zahir, PIETTE, Jean-Charles

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  6. 6
    The plasma homocysteine/creatinine ratio can be used to study the implication of (C677T) MTHFR genetic variants in homocysteine homeostasis

    The plasma homocysteine/creatinine ratio can be used to study the implication of (C677T) MTHFR genetic variants in homocysteine homeostasis by Cuer, M, Barrot, S, Jaureguy, F, Manéné, D, Durand, G, Le Moël, G

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