Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletionStefan Vielhaber, Wolfram S. Kunz, Grażyna Dębska–Vielhaber et al.|Acta Neuropathologica|2012Cited by 91
Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengersGrażyna Dębska–Vielhaber, Wolfram S. Kunz, Irina Miller et al.|Experimental Neurology|2021Cited by 28
Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical courseStefan Vielhaber, Wolfram S. Kunz, H. Feistner et al.|Journal of Clinical Neuroscience|2004Cited by 24
Defective Mitochondrial Oxidative Phosphorylation in Myopathies with Tubular Aggregates Originating from Sarcoplasmic ReticulumStefan Vielhaber, Wolfram S. Kunz, Rolf Schröder et al.|Journal of Neuropathology & Experimental Neurology|2001Cited by 22
Facioscapulohumeral muscular dystrophy with <i>Eco</i>RI/<i>Bln</i>I fragment size of more than 32 kbStefan Vielhaber, Thomas Bettecken, H. Feistner et al.|Muscle & Nerve|2002Cited by 13