Kunz WS - Search Results

1

Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging?

Zsurka G, Peeva V, Kotlyar A, Kunz WS. Zsurka G, et al. Among authors: kunz ws. Genes (Basel). 2018 Mar 21;9(4):175. doi: 10.3390/genes9040175. Genes (Basel). 2018. PMID: 29561808 Free PMC article. Review.

2

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: kunz ws. 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.

3

Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation.

Boes M, Bauer J, Urbach H, Elger CE, Frank S, Baron M, Zsurka G, Kunz WS, Kornblum C. Boes M, et al. Among authors: kunz ws. Seizure. 2009 Apr;18(3):232-4. doi: 10.1016/j.seizure.2008.08.003. Epub 2008 Sep 9. Seizure. 2009. PMID: 18783964 Free article.

4

Mitochondrial involvement in temporal lobe epilepsy.

Kudin AP, Zsurka G, Elger CE, Kunz WS. Kudin AP, et al. Among authors: kunz ws. Exp Neurol. 2009 Aug;218(2):326-32. doi: 10.1016/j.expneurol.2009.02.014. Epub 2009 Mar 5. Exp Neurol. 2009. PMID: 19268667 Review.

5

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene.

Zsurka G, Hampel KG, Nelson I, Jardel C, Mirandola SR, Sassen R, Kornblum C, Marcorelles P, Lavoué S, Lombès A, Kunz WS. Zsurka G, et al. Among authors: kunz ws. Neurology. 2010 Feb 9;74(6):507-12. doi: 10.1212/WNL.0b013e3181cef7ab. Neurology. 2010. PMID: 20142618

6

Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans.

Zsurka G, Kudina T, Peeva V, Hallmann K, Elger CE, Khrapko K, Kunz WS. Zsurka G, et al. Among authors: kunz ws. BMC Evol Biol. 2010 Sep 2;10:270. doi: 10.1186/1471-2148-10-270. BMC Evol Biol. 2010. PMID: 20813043 Free PMC article.

7

Mitochondrial dysfunction in neurological disorders with epileptic phenotypes.

Zsurka G, Kunz WS. Zsurka G, et al. Among authors: kunz ws. J Bioenerg Biomembr. 2010 Dec;42(6):443-8. doi: 10.1007/s10863-010-9314-7. J Bioenerg Biomembr. 2010. PMID: 21069442 Review.

8

Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion.

Vielhaber S, Debska-Vielhaber G, Peeva V, Schoeler S, Kudin AP, Minin I, Schreiber S, Dengler R, Kollewe K, Zuschratter W, Kornblum C, Zsurka G, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Acta Neuropathol. 2013 Feb;125(2):245-56. doi: 10.1007/s00401-012-1036-y. Epub 2012 Aug 28. Acta Neuropathol. 2013. PMID: 22926664

9

Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease.

Kornblum C, Nicholls TJ, Haack TB, Schöler S, Peeva V, Danhauser K, Hallmann K, Zsurka G, Rorbach J, Iuso A, Wieland T, Sciacco M, Ronchi D, Comi GP, Moggio M, Quinzii CM, DiMauro S, Calvo SE, Mootha VK, Klopstock T, Strom TM, Meitinger T, Minczuk M, Kunz WS, Prokisch H. Kornblum C, et al. Among authors: kunz ws. Nat Genet. 2013 Feb;45(2):214-9. doi: 10.1038/ng.2501. Epub 2013 Jan 13. Nat Genet. 2013. PMID: 23313956 Free PMC article.

10

Mitochondrial involvement in neurodegenerative diseases.

Zsurka G, Kunz WS. Zsurka G, et al. Among authors: kunz ws. IUBMB Life. 2013 Mar;65(3):263-72. doi: 10.1002/iub.1126. Epub 2013 Jan 22. IUBMB Life. 2013. PMID: 23341346 Free article. Review.

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