Detalhe da pesquisa
1.
Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.
Parkinsonism Relat Disord
; 111: 105441, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37201327
2.
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China.
NPJ Parkinsons Dis
; 9(1): 76, 2023 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37198191
3.
Deletion of Dcf1 Reduces Amyloid-ß Aggregation and Mitigates Memory Deficits.
J Alzheimers Dis
; 81(3): 1181-1194, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33896839