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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation.
Mackenzie IR, Ansorge O, Strong M, Bilbao J, Zinman L, Ang LC, Baker M, Stewart H, Eisen A, Rademakers R, Neumann M. Mackenzie IR, et al. Among authors: ang lc. Acta Neuropathol. 2011 Jul;122(1):87-98. doi: 10.1007/s00401-011-0838-7. Epub 2011 May 21. Acta Neuropathol. 2011. PMID: 21604077 Free PMC article.
Everything Old is New Again.
Florendo-Cumbermack A, Selchen D, Morrow SA, Sharma M, Steven D, Ang LC, Casserly C, Burneo J, Kremenchutzky M, Hammond R. Florendo-Cumbermack A, et al. Among authors: ang lc. Can J Neurol Sci. 2016 Jan;43(1):213-8. doi: 10.1017/cjn.2015.309. Can J Neurol Sci. 2016. PMID: 27182570 No abstract available.
Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype.
Volkening K, Farhan SMK, Kao J, Leystra-Lantz C, Ang LC, McIntyre A, Wang J, Hegele RA, Strong MJ. Volkening K, et al. Among authors: ang lc. Mol Cell Biochem. 2021 Jul;476(7):2633-2650. doi: 10.1007/s11010-021-04103-7. Epub 2021 Mar 4. Mol Cell Biochem. 2021. PMID: 33661429 Free PMC article.
185 results