AAAAAA

   
Results: 1-16 |
Results: 16
Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum
Authors: Vielhaber, S Schroder, R Winkler, K Weis, S Sailer, M Feistner, H Heinze, HJ Schroder, JM Kunz, WS
Citation: S. Vielhaber et al., Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum, J NE EXP NE, 60(11), 2001, pp. 1032-1040
Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activity
Authors: Schwarz, CS Evert, BO Seyfried, J Schaupp, M Kunz, WS Vielhaber, S Klockgether, T Wullner, U
Citation: Cs. Schwarz et al., Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activity, BIOC BIOP R, 280(4), 2001, pp. 1021-1027
Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures
Authors: Muller, HD Vielhaber, S Brunn, A Schroder, JM
Citation: Hd. Muller et al., Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures, ACT NEUROP, 102(1), 2001, pp. 27-35
Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita
Authors: Vielhaber, S Feistner, H Schneider, W Weis, J Kunz, WS
Citation: S. Vielhaber et al., Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita, PED NEUROL, 22(1), 2000, pp. 53-56
Mitochondrial complex I deficiency in the epileptic focus of patients withtemporal lobe epilepsy
Authors: Kunz, WS Kudin, AP Vielhaber, S Blumcke, I Zuschratter, W Schramm, J Beck, H Elger, CE
Citation: Ws. Kunz et al., Mitochondrial complex I deficiency in the epileptic focus of patients withtemporal lobe epilepsy, ANN NEUROL, 48(5), 2000, pp. 766-773
Frontal-executive dysfunction in early onset cerebellar ataxia of Holmes' type
Authors: Vielhaber, S Ebert, AD Feistner, H Herrmann, M
Citation: S. Vielhaber et al., Frontal-executive dysfunction in early onset cerebellar ataxia of Holmes' type, CLIN NEUROL, 102(2), 2000, pp. 102-105
Muscle fibres: applications for the study of the metabolic consequences ofenzyme deficiencies in skeletal muscle
Authors: Vielhaber, S Kudin, A Schroder, R Elger, CE Kunz, WS
Citation: S. Vielhaber et al., Muscle fibres: applications for the study of the metabolic consequences ofenzyme deficiencies in skeletal muscle, BIOCH SOC T, 28, 2000, pp. 159-164
New insights into the metabolic consequences of large-scale mtDNA deletions: A quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle
Authors: Schroder, R Vielhaber, S Wiedemann, FR Kornblum, C Papassotiropoulos, A Broich, P Zierz, S Elger, CE Reichmann, H Seibel, P Klockgether, T Kunz, WS
Citation: R. Schroder et al., New insights into the metabolic consequences of large-scale mtDNA deletions: A quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle, J NE EXP NE, 59(5), 2000, pp. 353-360
Flux control of cytochrome c oxidase in human skeletal muscle
Authors: Kunz, WS Kudin, A Vielhaber, S Elger, CE Attardi, G Villani, G
Citation: Ws. Kunz et al., Flux control of cytochrome c oxidase in human skeletal muscle, J BIOL CHEM, 275(36), 2000, pp. 27741-27745
Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
Authors: Vielhaber, S Kunz, D Winkler, K Wiedemann, FR Kirches, E Feistner, H Heinze, HJ Elger, CE Schubert, W Kunz, WS
Citation: S. Vielhaber et al., Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis, BRAIN, 123, 2000, pp. 1339-1348
Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples
Authors: Wiedemann, FR Vielhaber, S Schroder, R Elger, CE Kunz, WS
Citation: Fr. Wiedemann et al., Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples, ANALYT BIOC, 279(1), 2000, pp. 55-60
The quantification of motor units in carpal tunnel syndrome by motor unit estimation
Authors: Gonschorek, AS Awiszus, F Vielhaber, S Feistner, H
Citation: As. Gonschorek et al., The quantification of motor units in carpal tunnel syndrome by motor unit estimation, KLIN NEUROP, 30(1), 1999, pp. 22-25
Effects of the amplitude threshold on the separability of neuropathic and myopathic from normal EMG using parameters of the turns amplitude analysis
Authors: Strempel, J Vielhaber, S Tschernitschek, H Hinrichs, H Awiszus, F Feistner, H
Citation: J. Strempel et al., Effects of the amplitude threshold on the separability of neuropathic and myopathic from normal EMG using parameters of the turns amplitude analysis, CLIN NEU, 110(6), 1999, pp. 1139-1143
Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy
Authors: Kirches, E Winkler, K Vielhaber, S Michael, M Warich-Kirches, M von Bossanyi, P Plate, I Kunz, WS Szibor, R Feistner, H Dietzmann, K
Citation: E. Kirches et al., Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy, PATHOBIOLOG, 67(4), 1999, pp. 214-218
Differential diagnosis of proximal muscular weakness: Osteomalacial myopathy
Authors: Vielhaber, S Riedemann, C Pottag, G Klose, S Kekow, J Schroder, JM Sailer, M Feistner, H
Citation: S. Vielhaber et al., Differential diagnosis of proximal muscular weakness: Osteomalacial myopathy, AKT NEUROL, 26(5), 1999, pp. 236-239
Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis
Authors: Vielhaber, S Winkler, K Kirches, E Kunz, D Buchner, M Feistner, H Elger, CE Ludolph, AC Riepe, MW Kunz, WS
Citation: S. Vielhaber et al., Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis, J NEUR SCI, 169(1-2), 1999, pp. 133-139
Risultati: 1-16 |