Bilaketaren emaitzak - Melanie Schranz

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  1. 1
    Ferroportin disease: A systematic meta-analysis of clinical and molecular findings

    Ferroportin disease: A systematic meta-analysis of clinical and molecular findings nork Roman Mayr, Andreas Janecke, Melanie Schranz, William J. Griffiths, Wolfgang Vogel, Antonello Pietrangelo, Heinz Zoller

    Argitaratua 2010
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  2. 2
    Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation

    Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation nork Armin Finkenstedt, Elisabeth Wolf, Elmar Höfner, Bethina Isasi Gasser, Sylvia Bösch, Rania Bakry, Marc Creus, Christian Kremser, Michael Schocke, Milan Theurl, Patrizia Moser, Melanie Schranz, Guenther K. Bonn, Werner Poewe, Wolfgang Vogel, Andreas Janecke, Heinz Zoller

    Argitaratua 2010
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  3. 3
    Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea

    Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea nork Peter Heinz‐Erian, Thomas Müller, Birgit Krabichler, Melanie Schranz, Christian Becker, Franz Rüschendorf, Peter Nürnberg, Bernard C. Rossier, Mihailo Vujic, I W Booth, Christer Holmberg, Cisca Wijmenga, Giedre Grigelioniené, C. M. F. Kneepkens, Štefan Rosipal, Martin Mistrík, Matthias Kappler, L. Michaud, Ludwig-Christoph Dóczy, Victoria Mok Siu, Marie Krantz, Heinz Zoller, Gerd Utermann, Andreas Janecke

    Argitaratua 2009
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