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Matthias Vorgerd
Matthias Vorgerd
Neurologie
Verified email at bergmannsheil.de
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Year
Nesprin-1 and-2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity
Q Zhang, C Bethmann, NF Worth, JD Davies, C Wasner, A Feuer, ...
Human molecular genetics 16 (23), 2816-2833, 2007
5942007
Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
G Bonne, E Mercuri, A Muchir, A Urtizberea, HM Becane, D Recan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2000
5582000
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
3412000
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
3212005
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
2472001
Creatine for treating muscle disorders
RA Kley, MA Tarnopolsky, M Vorgerd
Cochrane Database of Systematic Reviews, 2013
2442013
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
2302008
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
2182005
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
2102010
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
1812000
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
1602014
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
1592007
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
1521997
Filamin C-related myopathies: pathology and mechanisms
DO Fürst, LG Goldfarb, RA Kley, M Vorgerd, M Olivé, PFM van der Ven
Acta neuropathologica 125, 33-46, 2013
1332013
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
1292014
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
1202002
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
1162004
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
1092013
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P
MC Walter, P Reilich, A Huebner, D Fischer, R Schröder, M Vorgerd, ...
Brain 130 (6), 1485-1496, 2007
1082007
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
1042003
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