Resultados da busca - Mathieu Jablonski

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  1. 1
    Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome

    Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome por Fádi Fakhouri, Mathieu Jablonski, J. Lepercq, Jacques Blouin, Alexandra Benachi, Maryvonne Hourmant, Yves Pirson, Antoine Dürrbach, Jean‐Pierre Grünfeld, Bertrand Knebelmann, Véronique Frémeaux‐Bacchi

    Publicado em 2008
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  2. 2
    Autoreactive IgE Is Prevalent in Systemic Lupus Erythematosus and Is Associated with Increased Disease Activity and Nephritis

    Autoreactive IgE Is Prevalent in Systemic Lupus Erythematosus and Is Associated with Increased Disease Activity and Nephritis por Bárbara Dema, Christophe Pellefigues, Sarfaraz Hasni, Nathalie Gault, Chao Jiang, Tiffany K. Ricks, Michael Bonelli, Jörg Scheffel, Karim Sacré, Mathieu Jablonski, Delphine Gobert, T. Papo, Éric Daugas, Gabor G. Illei, Nicolas Charles, Juan Rivera

    Publicado em 2014
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  3. 3
    Renal Involvement in Cystic Fibrosis

    Renal Involvement in Cystic Fibrosis por Yasmina Yahiaoui, Mathieu Jablonski, D. Hubert, Helen Mosnier-Pudar, Laure-HeCombining Acute AccentleCombining Grave Accentne NoeCombining Diaeresisl, M. Stern, Dominique Grenet, Jean-Pierre GruCombining Diaeresisnfeld, Dominique Chauveau, Fádi Fakhouri

    Publicado em 2009
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  4. 4
    Immunoglobulin E plays an immunoregulatory role in lupus

    Immunoglobulin E plays an immunoregulatory role in lupus por Bárbara Dema, Nicolas Charles, Christophe Pellefigues, Tiffany K. Ricks, Ryo Suzuki, Chao Jiang, Jörg Scheffel, Sarfaraz Hasni, Victoria Hoffman, Mathieu Jablonski, Karim Sacré, Delphine Gobert, T. Papo, Éric Daugas, Steve P. Crampton, Silvia Bolland, Juan Rivera

    Publicado em 2014
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  5. 5
    Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign?

    Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign? por Maria Chiara Marinozzi, L Vergoz, Tania Rybkine, Stéphanie Ngo, Serena Bettoni, Anastas Pashov, Mathieu Cayla, Fanny Tabarin, Mathieu Jablonski, Christophe Hue, Richard J. Smith, Marina Noris, Lise Halbwachs‐Mecarelli, Roberta Donadelli, Véronique Frémeaux‐Bacchi, Lubka T. Roumenina

    Publicado em 2014
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  6. 6
    Gluten exacerbates IgA nephropathy in humanized mice through gliadin–CD89 interaction

    Gluten exacerbates IgA nephropathy in humanized mice through gliadin–CD89 interaction por Christina Papista, Sebastian M. Lechner, Sanae Ben Mkaddem, Marie-Bénédicte LeStang, Lilia Abbad, Julie Bex-Coudrat, Évangéline Pillebout, Jonathan Chemouny, Mathieu Jablonski, Martin Flamant, Éric Daugas, François Vrtovsnik, Minas Yiangou, Laureline Berthelot, Renato C. Monteiro

    Publicado em 2015
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  7. 7
    Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome

    Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome por Frank Bienaimé, Marie‐Agnès Dragon‐Durey, Catherine H. Régnier, Sara C. Nilsson, W. H. Kwan, Jacques Blouin, Mathieu Jablonski, Nicolas Renault, Marie‐Anne Rameix‐Welti, Chantal Loirat, Catherine Sautès‐Fridman, Bruno O. Villoutreix, Anna M. Blom, Véronique Frémeaux‐Bacchi

    Publicado em 2009
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  8. 8
    Prostaglandin D2 amplifies lupus disease through basophil accumulation in lymphoid organs

    Prostaglandin D2 amplifies lupus disease through basophil accumulation in lymphoid organs por Christophe Pellefigues, Bárbara Dema, Yasmine Lamri, Fanny Saidoune, Nathalie Chavarot, Charlotte Lohéac, Emeline Pacreau, Michaël Dussiot, Caroline Bidault, Florian Marquet, Mathieu Jablonski, Jonathan Chemouny, F. Jouan, Antoine Dossier, Marie‐Paule Chauveheid, Delphine Gobert, T. Papo, Hajime Karasuyama, Karim Sacré, Éric Daugas, Nicolas Charles

    Publicado em 2018
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  9. 9
    Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

    Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome por Lubka T. Roumenina, Mathieu Jablonski, Christophe Hue, Jacques Blouin, Jordan D. Dimitrov, Marie‐Agnès Dragon‐Durey, Mathieu Cayla, Wolf H. Fridman, Marie-Alice Macher, David Ribes, L Moulonguet, Lionel Rostaing, Simon C. Satchell, Peter W. Mathieson, Catherine Sautès‐Fridman, Chantal Loirat, Catherine H. Régnier, Lise Halbwachs‐Mecarelli, Véronique Frémeaux‐Bacchi

    Publicado em 2009
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