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Journal of Neuromuscular Diseases|May 31, 2021
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth NeuropathyElisabeth Schorling, Katja C Senn, Simone Thiele, et al.Journal of Child Neurology|April 3, 2009
Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic optionCelina von Stülpnagel, Peter Reilich, Andreas Straube, et al.Neuromuscular Disorders : NMD|May 30, 2006
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophyJuliane S Müller, Henriett Piko, Benedikt G H Schoser, et al.Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.Muscle & Nerve|February 3, 2004
Muscle pathology in 57 patients with myotonic dystrophy type 2Benedikt G H Schoser, Christiane Schneider-Gold, Wolfram Kress, et al.Journal of Neurology|February 11, 2010
Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathyPeter Reilich, Nicolai Schramm, Benedikt Schoser, et al.Orphanet Journal of Rare Diseases|February 15, 2013
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trialMaggie C Walter, Peter Reilich, Simone Thiele, et al.Journal of Neurology|July 31, 2024
Diagnostic accuracy and confounders of vagus nerve ultrasound in amyotrophic lateral sclerosis-a single-center case series and pooled individual patient data meta-analysisKatharina J Müller, Moritz L Schmidbauer, Sonja Schönecker, et al.Neuromuscular Disorders : NMD|May 28, 2008
Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathiesKatharina Strach, Torsten Sommer, Christian Grohé, et al.Neurological Research and Practice|December 15, 2022
ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scaleAndré Maier, Matthias Boentert, Peter Reilich, et al.Pageof 5