Rezultati pretrage - Heldt, Katrin

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  1. 1
    Precision treatment of Singleton Merten syndrome with ruxolitinib: a case report

    Precision treatment of Singleton Merten syndrome with ruxolitinib: a case report od Broser, Philip, von Mengershausen, Ursula, Heldt, Katrin, Bartholdi, Deborah, Braun, Dominique, Wolf, Christine, Lee-Kirsch, Min Ae

    Izdano 2022
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  2. 2
    Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency

    Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency od Santosa, David, Donner, Markus G., vom Dahl, Stephan, Fleisch, Markus, Hoehn, Thomas, Mayatepek, Ertan, Heldt, Katrin, Niehues, Tim, Häussinger, Dieter

    Izdano 2017
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