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Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.
Sun YM, Gan LH, Peng F, Zhou XY, Chen QS, Liu FT, Tang YL, Wu P, Lu JY, Ge JJ, Yen TC, Zuo CT, Song B, Wu JJ, Wang J. Sun YM, et al. Among authors: zhou xy. Parkinsonism Relat Disord. 2023 Jun;111:105441. doi: 10.1016/j.parkreldis.2023.105441. Epub 2023 May 12. Parkinsonism Relat Disord. 2023. PMID: 37201327
Uncovering distinct progression patterns of tau deposition in progressive supranuclear palsy using [18F]Florzolotau PET imaging and subtype/stage inference algorithm.
Hong J, Lu J, Liu F, Wang M, Li X, Clement C, Lopes L, Brendel M, Rominger A, Yen TC, Guan Y, Tian M, Wang J, Zuo C, Shi K; Progressive Supranuclear Palsy Neuroimage Initiative (PSPNI). Hong J, et al. EBioMedicine. 2023 Nov;97:104835. doi: 10.1016/j.ebiom.2023.104835. Epub 2023 Oct 14. EBioMedicine. 2023. PMID: 37839135 Free PMC article.
1,313 results