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Ideggyogyaszati Szemle|May 12, 2005
[Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family]Rita Horváth, Maggie C Walter, Hanns Lochmüller, et al.Neuromuscular Disorders : NMD|March 30, 2010
Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian familyAndrea Stober, Angelo Aleo, Valerio Kuhl, et al.Der Nervenarzt|November 20, 2020
[Expert recommendation: treatment of nonambulatory patients with Duchenne muscular dystrophy]Guenther Bernert, Andreas Hahn, Cornelia Köhler, et al.Fortschritte Der Neurologie-Psychiatrie|December 18, 2019
[Spinal Muscular Atrophy - expert recommendations for the use of nusinersen in adult patients]Tim Hagenacker, Andreas Hermann, Christoph Kamm, et al.Ophthalmology|July 6, 2004
Ocular features of the congenital cataracts facial dysmorphism neuropathy syndromeAndrea Müllner-Eidenböck, Elisabeth Moser, Nina Klebermass, et al.Journal of Neuromuscular Diseases|July 10, 2023
Closing the Gap - Detection of 5q-Spinal Muscular Atrophy by Short-Read Next-Generation Sequencing and Unexpected Results in a Diagnostic Patient CohortStephanie Kleinle, Veronika Scholz, Anna Benet-Pagés, et al.BMC Musculoskeletal Disorders|January 18, 2013
A new web-based method for automated analysis of muscle histologyCordula Pertl, Markus Eblenkamp, Anja Pertl, et al.Neurology|September 5, 2014
Long-term follow-up in patients with CCFDN syndromeMaggie C Walter, Günther Bernert, Uta Zimmermann, et al.The Cochrane Database of Systematic Reviews|June 5, 2022
Treatment for inclusion body myositisMichael R Rose, Katherine Jones, Kevin Leong, et al.Journal of Neurology|July 20, 2004
The long-term outcome of anti-Jo-1-positive inflammatory myopathiesMichael Späth, Mira Schröder, Beate Schlotter-Weigel, et al.Pageof 17