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Distinction of sporadic and familial forms of ALS based on mitochondrial characteristics.
Walczak J, Dębska-Vielhaber G, Vielhaber S, Szymański J, Charzyńska A, Duszyński J, Szczepanowska J. Walczak J, et al. Among authors: vielhaber s. FASEB J. 2019 Mar;33(3):4388-4403. doi: 10.1096/fj.201801843R. Epub 2018 Dec 14. FASEB J. 2019. PMID: 30550341
These findings could be a first step in development of a new tool for predicting sporadic and familial forms of ALS and could contribute to knowledge of its pathophysiology.-Walczak, J., Debska-Vielhaber, G., Vielhaber, S., Szymanski, J., Charzynska, A., Dusz …
These findings could be a first step in development of a new tool for predicting sporadic and familial forms of ALS and could contribute to …
Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy.
Vielhaber S, Niessen HG, Debska-Vielhaber G, Kudin AP, Wellmer J, Kaufmann J, Schönfeld MA, Fendrich R, Willker W, Leibfritz D, Schramm J, Elger CE, Heinze HJ, Kunz WS. Vielhaber S, et al. Epilepsia. 2008 Jan;49(1):40-50. doi: 10.1111/j.1528-1167.2007.01280.x. Epub 2007 Sep 5. Epilepsia. 2008. PMID: 17822430 Free article.
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. Acta Neuropathol. 2013 Feb;125(2):245-56. doi: 10.1007/s00401-012-1036-y. Epub 2012 Aug 28. Acta Neuropathol. 2013. PMID: 22926664
182 results