Resultats de la cerca - D Pongratz

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  1. 1
    Skeletal muscle sonography: a correlative study of echogenicity and morphology

    Skeletal muscle sonography: a correlative study of echogenicity and morphology per Kerstin Reimers, C. D. Reimers, Stephan N. Wagner, I. Paetzke, D. Pongratz

    Publicat 1993
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  2. 2
    Molecular basis of AMP deaminase deficiency in skeletal muscle.

    Molecular basis of AMP deaminase deficiency in skeletal muscle. per Takayuki Morisaki, Matthias Groß, Hiroko Morisaki, D. Pongratz, N. Zöllner, E W Holmes

    Publicat 1992
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  3. 3
    A defective Intramolecular Autoactivation Cascade May Cause the Reduced Kinase Activity of the Skeletal Muscle Insulin Receptor from Patients with Non-insulin-dependent Diabetes Mellitus

    A defective Intramolecular Autoactivation Cascade May Cause the Reduced Kinase Activity of the Skeletal Muscle Insulin Receptor from Patients with Non-insulin-dependent Diabetes Me... per B. Obermaier–Kusser, Morris F. White, D. Pongratz, Zhe Su, B Ermel, C Mühlbacher, Hans-Ulrich Häring

    Publicat 1989
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  4. 4
    Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis.

    Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis. per Norbert Goebels, Dorothea Michaelis, Mélanie Engelhardt, Susanne Huber, Axel Bender, D. Pongratz, M. A. Johnson, Hartmut Wekerle, Jürg Tschopp, Dieter E. Jenne, Reinhard Hohlfeld

    Publicat 1996
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  5. 5
    Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA<sup>ser(UCN)</sup> gene

    Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA<sup>ser(UCN)</sup> gene per Michaela Jaksch, Thomas Klopstock, G Kurlemann, Marion Dörner, Sabine Hofmann, Stephanie Kleinle, Stefan Hegemann, M Weissert, Josef Müller‐Höcker, D. Pongratz, Klus‐Dieter Gerbitz

    Publicat 1998
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  6. 6
    FKRP (826C&gt;A) frequently causes limb-girdle muscular dystrophy in German patients

    FKRP (826C&gt;A) frequently causes limb-girdle muscular dystrophy in German patients per Maggie C. Walter, Jens A. Petersen, Rolf Stucka, Dirk Fischer, Rolf Schröder, Matthias Vorgerd, Anja Schroers, Herbert Schreiber, C. Oliver Hanemann, U Knirsch, Angela Rosenbohm, Angela Huebner, Nina Barišić, Rita Horváth, Sámuel Komoly, Peter Reilich, Wolfgang Müller‐Felber, D Pongratz, Juliane S. Müller, Ennes A. Auerswald, Hanns Lochmüller

    Publicat 2004
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