検索結果 - Gundula Notheis

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  1. 1
    Common Variable Immunodeficiency Disorders in Children: Delayed Diagnosis Despite Typical Clinical Presentation

    Common Variable Immunodeficiency Disorders in Children: Delayed Diagnosis Despite Typical Clinical Presentation 著者: Simon Urschel, Lale Kayikci, Uwe Wintergerst, Gundula Notheis, Annette Jansson, Bernd H. Belohradsky

    出版事項 2009
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  2. 2
    Antiviral efficacy, tolerability and pharmacokinetics of efavirenz in an unselected cohort of HIV-infected children

    Antiviral efficacy, tolerability and pharmacokinetics of efavirenz in an unselected cohort of HIV-infected children 著者: Uwe Wintergerst, Florian Hoffmann, Annette Jansson, Gundula Notheis, K Huß, Michael Kurowski, Dylan Burger

    出版事項 2008
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  3. 3
    ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia

    ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia 著者: Christie‐Ann McCarl, Capucine Pïcard, Sara Khalil, Takumi Kawasaki, Jens Röther, Alexander Papolos, Jeffery L. Kutok, Claire Hivroz, F Ledeist, Katrin Plogmann, Stephan Ehl, Gundula Notheis, Michael H. Albert, Bernd H. Belohradsky, Janbernd Kirschner, Anjana Rao, Alain Fischer, Stefan Feske

    出版事項 2009
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    Artigo
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  4. 4
    The German national registry for primary immunodeficiencies (PID)

    The German national registry for primary immunodeficiencies (PID) 著者: Benjamin Gathmann, Sigune Goldacker, Marion Klima, B. H. Belohradsky, Gundula Notheis, Stephan Ehl, Henrike Ritterbusch, Ulrich Baumann, Almut Meyer‐Bahlburg, T Witte, R. E. Schmidt, Michael Borte, Stephan Borte, R. Linde, Ralf Schubert, K. Bienemann, H.‐J. Laws, Gregor Dueckers, Joachim Roesler, Tobias Rothoeft, Renate Krüger, E. Scharbatke, Katja Masjosthusmann, JC Wasmuth, Olga Moser, Peter K. Kaiser, U. Gross‐Wieltsch, Carl Friedrich Classen, Gerd Horneff, Veronika Reiser, Nadine Binder, Salhab el Helou, Christoph Klein, Bodo Grimbacher, Gerhard Kindle

    出版事項 2013
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  5. 5
    X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

    X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease 著者: Claire Booth, Kimberly Gilmour, Paul Veys, Andrew R. Gennery, Mary Slatter, Helen Chapel, Paul T. Heath, Colin G. Steward, Owen Smith, A. O’Meara, Hilary Kerrigan, Nizar Mahlaoui, Marina Cavazzana, Alain Fischer, Despina Moshous, Stéphane Blanche, Jana Pachlopnik Schmid, Sylvain Latour, Geneviève de Saint Basile, Michael H. Albert, Gundula Notheis, Nikolaus Rieber, Brigitte Strahm, Henrike Ritterbusch, Arjan C. Lankester, Nico G. Hartwig, Isabelle Meyts, Alessandro Plebani, Annarosa Soresina, Andrea Finocchi, Claudio Pignata, Emilia Cirillo, Sonia Bonanomi, Christina Peters, Krzysztof Kałwak, Srdjan Pašić, Petr Sedláček, Janez Jazbec, Hirokazu Kanegane, Kim E. Nichols, I. Celine Hanson, Neena Kapoor, Élie Haddad, Morton J. Cowan, Sharon Choo, Joanne Smart, Peter D. Arkwright, H. Bobby Gaspar

    出版事項 2010
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