Vielhaber S - Search Results

1

Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy.

Winter Y, Schepelmann K, Spottke AE, Claus D, Grothe C, Schröder R, Heuss D, Vielhaber S, Tackenberg B, Mylius V, Reese JP, Kiefer R, Schrank B, Oertel WH, Dodel R. Winter Y, et al. Among authors: vielhaber s. J Neurol. 2010 Sep;257(9):1473-81. doi: 10.1007/s00415-010-5549-9. Epub 2010 Apr 10. J Neurol. 2010. PMID: 20383521

2

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

3

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.

4

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

5

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

6

Effect of creatine supplementation on metabolite levels in ALS motor cortices.

Vielhaber S, Kaufmann J, Kanowski M, Sailer M, Feistner H, Tempelmann C, Elger CE, Heinze HJ, Kunz WS. Vielhaber S, et al. Exp Neurol. 2001 Dec;172(2):377-82. doi: 10.1006/exnr.2001.7797. Exp Neurol. 2001. PMID: 11716561

7

Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.

Schröder R, Kunz WS, Rouan F, Pfendner E, Tolksdorf K, Kappes-Horn K, Altenschmidt-Mehring M, Knoblich R, van der Ven PF, Reimann J, Fürst DO, Blümcke I, Vielhaber S, Zillikens D, Eming S, Klockgether T, Uitto J, Wiche G, Rolfs A. Schröder R, et al. Among authors: vielhaber s. J Neuropathol Exp Neurol. 2002 Jun;61(6):520-30. doi: 10.1093/jnen/61.6.520. J Neuropathol Exp Neurol. 2002. PMID: 12071635

8

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.

Vielhaber S, Varlamov DA, Kudina TA, Schröder R, Kappes-Horn K, Elger CE, Seibel M, Seibel P, Kunz WS. Vielhaber S, et al. J Neuropathol Exp Neurol. 2002 Oct;61(10):885-95. doi: 10.1093/jnen/61.10.885. J Neuropathol Exp Neurol. 2002. PMID: 12387454

9

Mitochondrial dysfunction in myofibrillar myopathy.

Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Reimann J, et al. Among authors: vielhaber s. Neuropathol Appl Neurobiol. 2003 Feb;29(1):45-51. doi: 10.1046/j.1365-2990.2003.00428.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581339

10

Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle?

Vielhaber S, Kudin A, Winkler K, Wiedemann F, Schröder R, Feistner H, Heinze HJ, Elger CE, Kunz WS. Vielhaber S, et al. Ann Neurol. 2003 May;53(5):686-7; author reply 687-8. doi: 10.1002/ana.10564. Ann Neurol. 2003. PMID: 12731009 No abstract available.

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