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Zeitschriftenartikel
Lukas, Katharina; Gutschmidt, Kristina 
ORCID: https://orcid.org/0000-0001-9891-5919; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131 und Wenninger, Stephan ORCID: https://orcid.org/0000-0001-8407-3642
(2023):
Evaluation of myotonometry for myotonia, muscle stiffness and elasticity in neuromuscular disorders.
In: Journal of Neurology, Bd. 270, Nr. 11: S. 5398-5407
[PDF, 922kB]
ORCID: https://orcid.org/0000-0001-9891-5919; Schoser, Benedikt ORCID: https://orcid.org/0000-0002-2757-8131 und Wenninger, Stephan ORCID: https://orcid.org/0000-0001-8407-3642
(2023):
Evaluation of myotonometry for myotonia, muscle stiffness and elasticity in neuromuscular disorders.
In: Journal of Neurology, Bd. 270, Nr. 11: S. 5398-5407
[PDF, 922kB]
Wenninger, Stephan; Gutschmidt, Kristina; Wirner, Corinna; Einvag, Krisztina; Montagnese, Federica und Schoser, Benedikt
(2021):
The impact of interrupting enzyme replacement therapy in late-onset Pompe disease.
In: Journal of neurology
[PDF, 711kB]
Gutschmidt, Kristina; Musumeci, Olimpia; Diaz-Manera, Jordi; Chien, Yin-Hsiu; Knop, Karl Christian; Wenninger, Stephan; Montagnese, Federica; Pugliese, Alessia; Tavilla, Graziana; Alonso-Perez, Jorge; Hwu, Paul Wuh-Liang; Toscano, Antonio und Schoser, Benedikt
(2021):
STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfa.
In: Journal of Neurology, Bd. 268, Nr. 7: S. 2482-2492
Wenninger, Stephan; Cumming, Sarah A.; Gutschmidt, Kristina; Okkersen, Kees; Jimenez-Moreno, Aura Cecilia; Daidj, Ferroudja; Lochmüller, Hanns; Hogarth, Fiona; Knoop, Hans; Bassez, Guillaume; Monckton, Darren G.; Engelen, Baziel G. M. van und Schoser, Benedikt
(2021):
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1.
In: Neurology-Genetics, Bd. 7, Nr. 2, e572
Wenninger, Stephan; Gutschmidt, Kristina; Wirner, Corinna; Einvag, Krisztina; Montagnese, Federica und Schoser, Benedikt
(2021):
The impact of interrupting enzyme replacement therapy in late-onset Pompe disease.
In: Journal of Neurology, Bd. 268, Nr. 8: S. 2943-2950