Vielhaber S - Search Results

1

Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP.

Schreiber S, Oldag A, Kornblum C, Kollewe K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S. Schreiber S, et al. Among authors: vielhaber s. Muscle Nerve. 2013 Mar;47(3):385-95. doi: 10.1002/mus.23681. Epub 2013 Feb 4. Muscle Nerve. 2013. PMID: 23381770

2

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis.

Wiedemann FR, Winkler K, Kuznetsov AV, Bartels C, Vielhaber S, Feistner H, Kunz WS. Wiedemann FR, et al. Among authors: vielhaber s. J Neurol Sci. 1998;156(1):65-72. doi: 10.1016/s0022-510x(98)00008-2. J Neurol Sci. 1998. PMID: 9559989

3

Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita.

Vielhaber S, Feistner H, Schneider W, Weis J, Kunz WS. Vielhaber S, et al. Pediatr Neurol. 2000 Jan;22(1):53-6. doi: 10.1016/s0887-8994(99)00097-1. Pediatr Neurol. 2000. PMID: 10669207

4

Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples.

Wiedemann FR, Vielhaber S, Schröder R, Elger CE, Kunz WS. Wiedemann FR, et al. Among authors: vielhaber s. Anal Biochem. 2000 Mar 1;279(1):55-60. doi: 10.1006/abio.1999.4434. Anal Biochem. 2000. PMID: 10683230

5

Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy.

Kirches E, Winkler K, Vielhaber S, Michael M, Warich-Kirches M, von Bossanyi P, Plate I, Kunz WS, Szibor R, Feistner H, Dietzmann K. Kirches E, et al. Among authors: vielhaber s. Pathobiology. 1999 Jul-Aug;67(4):214-8. doi: 10.1159/000028075. Pathobiology. 1999. PMID: 10738184

6

Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle.

Vielhaber S, Kudin A, Schröder R, Elger CE, Kunz WS. Vielhaber S, et al. Biochem Soc Trans. 2000 Feb;28(2):159-64. doi: 10.1042/bst0280159. Biochem Soc Trans. 2000. PMID: 10816119

7

Frontal-executive dysfunction in early onset cerebellar ataxia of Holmes' type.

Vielhaber S, Ebert AD, Feistner H, Herrmann M. Vielhaber S, et al. Clin Neurol Neurosurg. 2000 Jun;102(2):102-5. doi: 10.1016/s0303-8467(00)00068-8. Clin Neurol Neurosurg. 2000. PMID: 10817897

8

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis.

Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Vielhaber S, et al. Brain. 2000 Jul;123 ( Pt 7):1339-48. doi: 10.1093/brain/123.7.1339. Brain. 2000. PMID: 10869047 Clinical Trial.

9

New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle.

Schröder R, Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS. Schröder R, et al. Among authors: vielhaber s. J Neuropathol Exp Neurol. 2000 May;59(5):353-60. doi: 10.1093/jnen/59.5.353. J Neuropathol Exp Neurol. 2000. PMID: 10888364

10

Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum.

Vielhaber S, Schröder R, Winkler K, Weis S, Sailer M, Feistner H, Heinze HJ, Schröder JM, Kunz WS. Vielhaber S, et al. J Neuropathol Exp Neurol. 2001 Nov;60(11):1032-40. doi: 10.1093/jnen/60.11.1032. J Neuropathol Exp Neurol. 2001. PMID: 11706933

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