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Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect.
Niemann S, Joos H, Meyer T, Vielhaber S, Reuner U, Gleichmann M, Dengler R, Müller U. Niemann S, et al. Among authors: vielhaber s. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1186-8. doi: 10.1136/jnnp.2003.028324. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258228 Free PMC article.
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
Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP.
Schreiber S, Oldag A, Kornblum C, Kollewe K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S. Schreiber S, et al. Among authors: vielhaber s. Muscle Nerve. 2013 Mar;47(3):385-95. doi: 10.1002/mus.23681. Epub 2013 Feb 4. Muscle Nerve. 2013. PMID: 23381770
184 results