Kunz WS - Search Results

1

Birtel J, von Landenberg C, Gliem M, Gliem C, Reimann J, Kunz WS, Herrmann P, Betz C, Caswell R, Nesbitt V, Kornblum C, Charbel Issa P. Birtel J, et al. Among authors: kunz ws. Ophthalmol Retina. 2022 Jan;6(1):65-79. doi: 10.1016/j.oret.2021.02.017. Epub 2021 Jul 10. Ophthalmol Retina. 2022. PMID: 34257060 Free article.

2

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: kunz ws. J Neuropathol Exp Neurol. 2000 May;59(5):353-60. doi: 10.1093/jnen/59.5.353. J Neuropathol Exp Neurol. 2000. PMID: 10888364

3

[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: kunz ws. Klin Monbl Augenheilkd. 2004 Dec;221(12):1057-61. doi: 10.1055/s-2004-813830. Klin Monbl Augenheilkd. 2004. PMID: 15599814 German.

4

Dopamine transporter SPECT in patients with mitochondrial disorders.

Minnerop M, Kornblum C, Joe AY, Tatsch K, Kunz WS, Klockgether T, Wüllner U, Reinhardt MJ. Minnerop M, et al. Among authors: kunz ws. J Neurol Neurosurg Psychiatry. 2005 Jan;76(1):118-20. doi: 10.1136/jnnp.2004.040220. J Neurol Neurosurg Psychiatry. 2005. PMID: 15608010 Free PMC article.

5

[Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome : interdisciplinary diagnosis and therapy].

Wabbels B, Ali N, Kunz WS, Roggenkämper P, Kornblum C. Wabbels B, et al. Among authors: kunz ws. Ophthalmologe. 2008 Jun;105(6):550-6. doi: 10.1007/s00347-007-1643-5. Ophthalmologe. 2008. PMID: 18373100 German.

6

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.

7

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

8

Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery.

Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS. Niehusmann P, et al. Among authors: kunz ws. Epilepsy Behav. 2011 Jan;20(1):38-43. doi: 10.1016/j.yebeh.2010.11.008. Epub 2010 Dec 9. Epilepsy Behav. 2011. PMID: 21145289

9

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

10

Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation.

Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C. Tschampa HJ, et al. Among authors: kunz ws. J Neurol. 2013 Apr;260(4):1071-80. doi: 10.1007/s00415-012-6763-4. Epub 2012 Nov 30. J Neurol. 2013. PMID: 23196335

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

295 results

Search Page