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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.

Parkinsonism Relat Disord · 2023-05-12

DOI: 10.1016/j.parkreldis.2023.105441PMID: 37201327

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Longitudinal Synaptic Loss in Primary Tauopathies: An In Vivo [<sup>11</sup> C]UCB-J Positron Emission Tomography Study.

Holland N, Jones PS, Savulich G, Naessens M, Malpetti M, Whiteside DJ, Street D, Swann P, Hong YT, Fryer TD, Rittman T, Mulroy E, Aigbirhio FI, Bhatia KP, O'Brien JT, Rowe JB.

Mov Disord · 2023-05-12

DOI: 10.1002/mds.29421PMID: 37171832

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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