Detalhe da pesquisa
1.
Genetic Modifiers of Age at Onset for Amyotrophic Lateral Sclerosis: A Genome-Wide Association Study.
Ann Neurol
; 94(5): 933-941, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37528491
2.
Mutation screening of SPTLC1 and SPTLC2 in amyotrophic lateral sclerosis.
Hum Genomics
; 17(1): 28, 2023 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36966328
3.
Motor progression marker for newly diagnosed drug-naïve patients with Parkinson's disease: A resting-state functional MRI study.
Hum Brain Mapp
; 44(3): 901-913, 2023 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36250699
4.
Longitudinal evolution of sleep disturbances in early multiple system atrophy: a 2-year prospective cohort study.
BMC Med
; 21(1): 454, 2023 11 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37993943
5.
Plasma glial fibrillary acidic protein as a biomarker of disease progression in Parkinson's disease: a prospective cohort study.
BMC Med
; 21(1): 420, 2023 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37932720
6.
Cross-Ethnic Variant Screening and Burden Analysis of PTPA in Parkinson's Disease.
Mov Disord
; 38(6): 1099-1104, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046398
7.
Lack of association of TP73 rare variants with amyotrophic lateral sclerosis in a Chinese cohort.
Hum Genomics
; 16(1): 63, 2022 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36451215
8.
TBK1 variants in Chinese patients with amyotrophic lateral sclerosis: Genetic analysis and clinical features.
Eur J Neurol
; 30(10): 3079-3089, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37422901
9.
Disrupted topological organization of resting-state functional brain networks in Parkinson's disease patients with glucocerebrosidase gene mutations.
Neuroradiology
; 65(2): 361-370, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36269334
10.
Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population.
J Med Genet
; 59(9): 840-849, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34544842
11.
Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis.
Neurobiol Dis
; 175: 105907, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36280108
12.
Longitudinal evolution of motor and non-motor symptoms in early-stage multiple system atrophy: a 2-year prospective cohort study.
BMC Med
; 20(1): 446, 2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36397048
13.
Neurofilament Light Chain Predicts Disease Severity and Progression in Multiple System Atrophy.
Mov Disord
; 37(2): 421-426, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34719813
14.
Genetic Determinants of Survival in Parkinson's Disease in the Asian Population.
Mov Disord
; 37(8): 1624-1633, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35616254
15.
Mutation Screening of TFG in α-Synucleinopathy and Amyotrophic Lateral Sclerosis.
Mov Disord
; 37(8): 1756-1761, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35642252
16.
Spatial-temporal pattern of propagation in amyotrophic lateral sclerosis and effect on survival: A cohort study.
Eur J Neurol
; 29(11): 3177-3186, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35996987
17.
The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.
Eur J Neurol
; 29(11): 3218-3228, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35861376
18.
Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study.
Mov Disord
; 36(9): 2077-2084, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33884653
19.
Different resting-state network disruptions in newly diagnosed drug-naïve Parkinson's disease patients with mild cognitive impairment.
BMC Neurol
; 21(1): 327, 2021 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34433445
20.
Abnormal eye movements in spinocerebellar ataxia type 3.
BMC Neurol
; 21(1): 28, 2021 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33468086