Detalhe da pesquisa
1.
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy Study.
Mov Disord
; 37(9): 1807-1816, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36054272
2.
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.
Brain
; 143(1): 222-233, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31819945
3.
UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(6): e54, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33779694
4.
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(3): e25, 2021 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33793763
5.
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
Brain
; 133(Pt 12): 3510-8, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21106500
6.
[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 27(5): 501-5, 2010 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-20931525
7.
Different iron deposition patterns in akinetic/rigid-dominant and tremor-dominant Parkinson's disease.
Clin Neurol Neurosurg
; 198: 106181, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33022525
8.
Mutation analysis of CAPN1 in Chinese populations with spastic paraplegia and related neurodegenerative diseases.
J Neurol Sci
; 411: 116691, 2020 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31982778
9.
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Transl Neurodegener
; 9(1): 31, 2020 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32746945
10.
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
Mov Disord
; 24(13): 2007-11, 2009 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19672991
11.
[Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 26(4): 406-9, 2009 Aug.
Artigo
em Zh
| MEDLINE | ID: mdl-20017304
12.
[Effects of moxibustion on the structure and function of blood brain barrier in Alzheimer's disease model rats].
Zhongguo Ying Yong Sheng Li Xue Za Zhi
; 35(5): 443-446, 2019 Sep.
Artigo
em Zh
| MEDLINE | ID: mdl-31894678
13.
Safety and efficacy of valproic acid treatment in SCA3/MJD patients.
Parkinsonism Relat Disord
; 26: 55-61, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26997655
14.
SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.
PLoS One
; 8(1): e54214, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382880
15.
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders.
Neurobiol Aging
; 34(10): 2442.e11-7, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23726790
16.
Simple and sensitive determination of sparfloxacin in pharmaceuticals and biological samples by immunoassay.
J Pharm Anal
; 2(3): 214-219, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29403745
17.
Lower serum UA levels in Parkinson's disease patients in the Chinese population.
Neurosci Lett
; 514(2): 152-5, 2012 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22405811