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Brain : a Journal of Neurology|February 3, 2009
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1Joachim Schessl, Ana L Taratuto, Caroline Sewry, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
European Journal of Neurology|February 23, 2021
Impact of the coronavirus disease 2019 pandemic on stroke teleconsultations in Germany in the first half of 2020Christoph Vollmuth, Olga Miljukov, Mazen Abu-Mugheisib, et al.
The New England Journal of Medicine|October 5, 2022
Trial of Intravenous Immune Globulin in DermatomyositisRohit Aggarwal, Christina Charles-Schoeman, Joachim Schessl, et al.
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