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Lipid dysfunction and pathogenesis of multiple system atrophy.
Bleasel JM, Wong JH, Halliday GM, Kim WS. Bleasel JM, et al. Among authors: kim ws. Acta Neuropathol Commun. 2014 Feb 7;2:15. doi: 10.1186/2051-5960-2-15. Acta Neuropathol Commun. 2014. PMID: 24502382 Free PMC article. Review.
Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperone.
Lee JS, Kanai K, Suzuki M, Kim WS, Yoo HS, Fu Y, Kim DK, Jung BC, Choi M, Oh KW, Li Y, Nakatani M, Nakazato T, Sekimoto S, Funayama M, Yoshino H, Kubo SI, Nishioka K, Sakai R, Ueyama M, Mochizuki H, Lee HJ, Sardi SP, Halliday GM, Nagai Y, Lee PH, Hattori N, Lee SJ. Lee JS, et al. Among authors: kim dk, kim ws. Brain. 2019 Sep 1;142(9):2845-2859. doi: 10.1093/brain/awz205. Brain. 2019. PMID: 31312839
Cross-examining candidate genes implicated in multiple system atrophy.
Katzeff JS, Phan K, Purushothuman S, Halliday GM, Kim WS. Katzeff JS, et al. Among authors: kim ws. Acta Neuropathol Commun. 2019 Jul 24;7(1):117. doi: 10.1186/s40478-019-0769-4. Acta Neuropathol Commun. 2019. PMID: 31340844 Free PMC article. Review.
2,845 results