Elger CE - Search Results

1

Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.

Kudin AP, Baron G, Zsurka G, Hampel KG, Elger CE, Grote A, Weber Y, Lerche H, Thiele H, Nürnberg P, Schulz H, Ruppert AK, Sander T, Cheng Q, Arnér ES, Schomburg L, Seeher S, Fradejas-Villar N, Schweizer U, Kunz WS. Kudin AP, et al. Among authors: elger ce. Free Radic Biol Med. 2017 May;106:270-277. doi: 10.1016/j.freeradbiomed.2017.02.040. Epub 2017 Feb 21. Free Radic Biol Med. 2017. PMID: 28232204

2

Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice.

Kunz WS, Kuznetsov AV, Clark JF, Tracey I, Elger CE. Kunz WS, et al. Among authors: elger ce. J Neurochem. 1999 Apr;72(4):1580-5. doi: 10.1046/j.1471-4159.1999.721580.x. J Neurochem. 1999. PMID: 10098864 Free article.

3

Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats.

Kunz WS, Goussakov IV, Beck H, Elger CE. Kunz WS, et al. Among authors: elger ce. Brain Res. 1999 May 1;826(2):236-42. doi: 10.1016/s0006-8993(99)01279-2. Brain Res. 1999. PMID: 10224301

4

Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis.

Vielhaber S, Winkler K, Kirches E, Kunz D, Büchner M, Feistner H, Elger CE, Ludolph AC, Riepe MW, Kunz WS. Vielhaber S, et al. Among authors: elger ce. J Neurol Sci. 1999 Oct 31;169(1-2):133-9. doi: 10.1016/s0022-510x(99)00236-1. J Neurol Sci. 1999. PMID: 10540022

5

Quantitative investigation of mitochondrial function in single rat hippocampal slices: a novel application of high-resolution respirometry and laser-excited fluorescence spectroscopy.

Kudin A, Vielhaber S, Beck H, Elger CE, Kunz WS. Kudin A, et al. Among authors: elger ce. Brain Res Brain Res Protoc. 1999 Dec;4(3):329-34. doi: 10.1016/s1385-299x(99)00037-9. Brain Res Brain Res Protoc. 1999. PMID: 10592342

6

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

7

Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Lentze MJ, Propping P, Elger CE, Heils A. Haug K, et al. Among authors: elger ce. Epilepsy Res. 2000 Apr;39(2):127-32. doi: 10.1016/s0920-1211(99)00116-3. Epilepsy Res. 2000. PMID: 10759301

8

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: elger ce. Biochem Soc Trans. 2000 Feb;28(2):159-64. doi: 10.1042/bst0280159. Biochem Soc Trans. 2000. PMID: 10816119

9

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. Among authors: elger ce. Brain. 2000 Jul;123 ( Pt 7):1339-48. doi: 10.1093/brain/123.7.1339. Brain. 2000. PMID: 10869047 Clinical Trial.

10

Flux control of cytochrome c oxidase in human skeletal muscle.

Kunz WS, Kudin A, Vielhaber S, Elger CE, Attardi G, Villani G. Kunz WS, et al. Among authors: elger ce. J Biol Chem. 2000 Sep 8;275(36):27741-5. doi: 10.1074/jbc.M004833200. J Biol Chem. 2000. PMID: 10869362 Free article.

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