Schröder R - Search Results

1

Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism.

Zsurka G, Schröder R, Kornblum C, Rudolph J, Wiesner RJ, Elger CE, Kunz WS. Zsurka G, et al. Among authors: schroder r. J Med Genet. 2004 Dec;41(12):e124. doi: 10.1136/jmg.2004.022566. J Med Genet. 2004. PMID: 15591266 Free PMC article. No abstract available.

2

[Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)].

Kornblum C, Kunz WS, Klockgether T, Roggenkämper P, Schröder R. Kornblum C, et al. Among authors: schroder r. Klin Monbl Augenheilkd. 2004 Dec;221(12):1057-61. doi: 10.1055/s-2004-813830. Klin Monbl Augenheilkd. 2004. PMID: 15599814 German.

3

Metabolic consequences of a novel missense mutation of the mtDNA CO I gene.

Varlamov DA, Kudin AP, Vielhaber S, Schröder R, Sassen R, Becker A, Kunz D, Haug K, Rebstock J, Heils A, Elger CE, Kunz WS. Varlamov DA, et al. Among authors: schroder r. Hum Mol Genet. 2002 Aug 1;11(16):1797-805. doi: 10.1093/hmg/11.16.1797. Hum Mol Genet. 2002. PMID: 12140182

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. 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

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. Among authors: schroder r. Biochem Soc Trans. 2000 Feb;28(2):159-64. doi: 10.1042/bst0280159. Biochem Soc Trans. 2000. PMID: 10816119

6

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. Among authors: schroder r. J Neuropathol Exp Neurol. 2002 Oct;61(10):885-95. doi: 10.1093/jnen/61.10.885. J Neuropathol Exp Neurol. 2002. PMID: 12387454

7

Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Bosbach S, Kornblum C, Schröder R, Wagner M. Bosbach S, et al. Among authors: schroder r. Brain. 2003 May;126(Pt 5):1231-40. doi: 10.1093/brain/awg101. Brain. 2003. PMID: 12690061

8

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. Among authors: schroder r. 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.

9

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: schroder r. Anal Biochem. 2000 Mar 1;279(1):55-60. doi: 10.1006/abio.1999.4434. Anal Biochem. 2000. PMID: 10683230

10

[The interesting case No. 32. Secondary cricopharyngeal achalasia in underlying mitochondrial myopathy].

Broicher R, Kornblum C, Schröder R, Walther E. Broicher R, et al. Among authors: schroder r. Laryngorhinootologie. 2000 Mar;79(3):190-2. doi: 10.1055/s-2000-292. Laryngorhinootologie. 2000. PMID: 10763179 German. No abstract available.

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