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Oxidative stress in patients with Friedreich ataxia JB Schulz, T Dehmer, L Schols, H Mende, C Hardt, M Vorgerd, K Burk, ... Neurology 55 (11), 1719-1721, 2000 | 345 | 2000 |
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy M Vorgerd, PFM Van der Ven, V Bruchertseifer, T Löwe, RA Kley, ... The American Journal of Human Genetics 77 (2), 297-304, 2005 | 340 | 2005 |
Creatine for treating muscle disorders RA Kley, MA Tarnopolsky, M Vorgerd Cochrane Database of Systematic Reviews, 2013 | 260 | 2013 |
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease RC Betz, BGH Schoser, D Kasper, K Ricker, A Ramírez, V Stein, ... Nature genetics 28 (3), 218-219, 2001 | 253 | 2001 |
Distinct muscle imaging patterns in myofibrillar myopathies D Fischer, RA Kley, K Strach, C Meyer, T Sommer, K Eger, A Rolfs, ... Neurology 71 (10), 758-765, 2008 | 245 | 2008 |
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease C Saft, J Zange, J Andrich, K Müller, K Lindenberg, B Landwehrmeyer, ... Movement disorders: official journal of the Movement Disorder Society 20 (6 …, 2005 | 232 | 2005 |
De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy B Klauke, S Kossmann, A Gaertner, K Brand, I Stork, A Brodehl, ... Human molecular genetics 19 (23), 4595-4607, 2010 | 220 | 2010 |
Effects of follicular versus luteal phase-based strength training in young women E Sung, A Han, T Hinrichs, M Vorgerd, C Manchado, P Platen Springerplus 3, 1-10, 2014 | 199 | 2014 |
Creatine therapy in myophosphorylase deficiency (McArdle disease): a placebo-controlled crossover trial M Vorgerd, T Grehl, M Jäger, K Müller, G Freitag, T Patzold, N Bruns, ... Archives of Neurology 57 (7), 956-963, 2000 | 191 | 2000 |
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients RA Kley, Y Hellenbroich, PFM Van der Ven, DO Fürst, A Huebner, ... Brain 130 (12), 3250-3264, 2007 | 168 | 2007 |
Spinocerebellar ataxia type 2: genotype and phenotype in German kindreds L Schöls, S Gispert, M Vorgerd, AMM Vieira-Saecker, P Blanke, ... Archives of neurology 54 (9), 1073-1080, 1997 | 160 | 1997 |
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Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial J Diaz-Manera, PS Kishnani, H Kushlaf, S Ladha, T Mozaffar, V Straub, ... The Lancet Neurology 20 (12), 1012-1026, 2021 | 140 | 2021 |
Human myocytes are protected from titin aggregation-induced stiffening by small heat shock proteins S Kötter, A Unger, N Hamdani, P Lang, M Vorgerd, L Nagel-Steger, ... Journal of Cell Biology 204 (2), 187-202, 2014 | 135 | 2014 |
Effect of high-dose creatine therapy on symptoms of exercise intolerance in McArdle disease: double-blind, placebo-controlled crossover study M Vorgerd, J Zange, R Kley, T Grehl, A Hüsing, M Jäger, K Müller, ... Archives of neurology 59 (1), 97-101, 2002 | 124 | 2002 |
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial MC Walter, P Reilich, S Thiele, J Schessl, H Schreiber, K Reiners, ... Orphanet Journal of Rare Diseases 8, 1-15, 2013 | 118 | 2013 |
The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy S Züchner, M Vorgerd, E Sindern, JM Schröder Neuromuscular Disorders 14 (2), 147-157, 2004 | 118 | 2004 |
Consequences of a novel caveolin‐3 mutation in a large German family D Fischer, A Schroers, I Blümcke, H Urbach, K Zerres, W Mortier, ... Annals of Neurology: Official Journal of the American Neurological …, 2003 | 112 | 2003 |