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Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Molecular therapies in muscular dystrophies]Maggie C Walter, Peter ReilichJournal of Neuromuscular Diseases|March 8, 2021
Effect of Discontinuation of Nusinersen Treatment in Long-Standing SMA3Miriam Hiebeler, Angela Abicht, Peter Reilich, et al.Scientific Reports|January 5, 2023
Time to diagnosis of Duchenne muscular dystrophy in Austria and GermanyMiriam Hiebeler, Simone Thiele, Peter Reilich, et al.Neuromuscular Disorders : NMD|April 18, 2019
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian familyElena Ikenberg, Peter Reilich, Angela Abicht, et al.European Radiology|July 24, 2008
Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body MRI protocolNicolai Schramm, Christine Born, Sabine Weckbach, et al.Neuromuscular Disorders : NMD|October 27, 2021
Congenital myopathy and epidermolysis bullosa due to PLEC variantMaggie C Walter, Peter Reilich, Sabine Krause, et al.Orphanet Journal of Rare Diseases|May 6, 2016
Disease burden of spinal muscular atrophy in GermanyConstanze Klug, Olivia Schreiber-Katz, Simone Thiele, et al.Orphanet Journal of Rare Diseases|December 19, 2014
Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in GermanyOlivia Schreiber-Katz, Constanze Klug, Simone Thiele, et al.Neuromuscular Disorders : NMD|July 2, 2017
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patientElena Ikenberg, Ivan Karin, Birgit Ertl-Wagner, et al.Neuromuscular Disorders : NMD|February 23, 2010
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathyPeter Reilich, Benedikt Schoser, Nicolai Schramm, et al.Pageof 17