Search Results - Strigl-Pill, Nicola

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  1. 1
    36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy

    36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy by Regnery, Caroline, Kornblum, Cornelia, Hanisch, Frank, Vielhaber, Stefan, Strigl-Pill, Nicola, Grunert, Birgit, Müller-Felber, Wolfgang, Glocker, Franz Xaver, Spranger, Matthias, Deschauer, Marcus, Mengel, Eugen, Schoser, Benedikt

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  2. 2
    Toward deconstructing the phenotype of late-onset Pompe disease

    Toward deconstructing the phenotype of late-onset Pompe disease by Schüller, Angela, Wenninger, Stephan, Strigl-Pill, Nicola, Schoser, Benedikt

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  3. 3
    Toward Deconstructing the Phenotype of Late-Onset Pompe Disease: Advancements in Pompe Disease

    Toward Deconstructing the Phenotype of Late-Onset Pompe Disease: Advancements in Pompe Disease by SCHULLER, Angela, WENNINGER, Stephan, STRIGL-PILL, Nicola, SCHOSER, Benedikt

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  4. 4
    Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy

    Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy by Reilich, Peter, Schramm, Nicolai, Schoser, Benedikt, Schneiderat, Peter, Strigl-Pill, Nicola, Müller-Höcker, Josef, Kress, Wolfram, Ferbert, Andreas, Rudnik-Schöneborn, Sabine, Noth, Johannes, Lochmüller, Hanns, Weis, Joachim, Walter, Maggie C.

    Published in Journal of neurology
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