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Numerical deficits in a single case of basal ganglia dysfunction.
Zamarian L, Bodner T, Revkin SK, Benke T, Boesch S, Donnemiller E, Delazer M. Zamarian L, et al. Among authors: boesch s. Neurocase. 2009 Oct;15(5):390-404. doi: 10.1080/13554790902849156. Epub 2009 Apr 16. Neurocase. 2009. PMID: 19370479
Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a cathepsin D variant p.A58V.
Ehling R, Nosková L, Stránecký V, Hartmannová H, Přistoupilová A, Hodaňová K, Benke T, Kovacs GG, Ströbel T, Niedermüller U, Wagner M, Nachbauer W, Janecke A, Budka H, Boesch S, Kmoch S. Ehling R, et al. Among authors: boesch s. J Neurol Sci. 2013 Mar 15;326(1-2):75-82. doi: 10.1016/j.jns.2013.01.017. Epub 2013 Feb 13. J Neurol Sci. 2013. PMID: 23415546
Erythropoietin in Friedreich ataxia.
Mariotti C, Nachbauer W, Panzeri M, Poewe W, Taroni F, Boesch S. Mariotti C, et al. Among authors: boesch s. J Neurochem. 2013 Aug;126 Suppl 1:80-7. doi: 10.1111/jnc.12301. J Neurochem. 2013. PMID: 23859343 Free article. Review.
215 results