Detalhe da pesquisa
1.
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
2.
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis.
BMC Med
; 20(1): 209, 2022 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35754054
3.
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
4.
Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases.
BMC Med
; 19(1): 27, 2021 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33541344
5.
Camptocormia in patients with multiple system atrophy at different disease durations: frequency and related factors.
BMC Neurol
; 21(1): 181, 2021 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33910524
6.
Coding mutations in NUS1 contribute to Parkinson's disease.
Proc Natl Acad Sci U S A
; 115(45): 11567-11572, 2018 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30348779
7.
Altered oligomeric states in pathogenic ALS2 variants associated with juvenile motor neuron diseases cause loss of ALS2-mediated endosomal function.
J Biol Chem
; 293(44): 17135-17153, 2018 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30224357
8.
Genome-wide association study of Parkinson's disease in East Asians.
Hum Mol Genet
; 26(1): 226-232, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28011712
9.
Functional links between SQSTM1 and ALS2 in the pathogenesis of ALS: cumulative impact on the protection against mutant SOD1-mediated motor dysfunction in mice.
Hum Mol Genet
; 25(15): 3321-3340, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27439389
10.
Impact of sleep-related breathing disorder on motor and non-motor symptoms in multiple system atrophy.
Sleep Breath
; 22(4): 981-987, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29380098
11.
Enrichment of rare variants of BIN1 but not APOE genes in Chinese patients with Parkinson's disease.
J Intern Med
; 291(5): 698-701, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34982487
12.
White matter microstructure damage in tremor-dominant Parkinson's disease patients.
Neuroradiology
; 59(7): 691-698, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28540401
13.
C9ORF72 repeat expansions in Chinese patients with Parkinson's disease and multiple system atrophy.
J Neural Transm (Vienna)
; 123(11): 1341-1345, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27473499
14.
Assessment of a multiple biomarker panel for diagnosis of amyotrophic lateral sclerosis.
BMC Neurol
; 16: 173, 2016 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27634542
15.
A novel nonsense mutation in the TYMP gene causing MNGIE with multiple intracranial hemorrhages on brain MRI.
Neurol Sci
; 42(5): 2119-2122, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33210226
16.
Association analysis of the GRN rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis.
Int J Neurosci
; 126(10): 947-54, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26303052
17.
The trajectory of disturbed resting-state cerebral function in Parkinson's disease at different Hoehn and Yahr stages.
Hum Brain Mapp
; 36(8): 3104-16, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25959682
18.
Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.
Neurol Sci
; 36(10): 1903-6, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26058955
19.
Impact of Frontal Lobe Function and Behavioral Changes on Health-Related Quality of Life in Patients with Parkinson's Disease: A Cross-Sectional Study from Southwest China.
Eur Neurol
; 74(3-4): 147-53, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26417992
20.
The serum lipid profile of Parkinson's disease patients: a study from China.
Int J Neurosci
; 125(11): 838-44, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25340257