Detalles de la búsqueda
1.
Research progress of oculomotor disorder in Parkinson's disease / 中华神经科杂志
Chinese Journal of Neurology
; (12): 143-146, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-734906
2.
Analysis of body mass index changes in Parkinson's disease and its association with disease severity / 中国医师杂志
Journal of Chinese Physician
; (12): 9-11, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705769
3.
Study on the clinical features and related factors of constipation in patients with Parkinson's disease / 中国医师杂志
Journal of Chinese Physician
; (12): 6-8, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705768
4.
The clinical characteristics and risk factors of frozen gait in Parkinson's disease / 中国医师杂志
Journal of Chinese Physician
; (12): 35-37,41, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705775
5.
Study on fatigue symptoms and related factors in Parkinson's disease patients / 中国医师杂志
Journal of Chinese Physician
; (12): 24-27, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705772
6.
Study on the clinical features and related factors of cognitive impairment in Parkinson's disease / 中国医师杂志
Journal of Chinese Physician
; (12): 12-15, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705770
7.
Progress in genetic research on essential tremor / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 767-771, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-344178
8.
Genetic analysis of P387L mutation in SLC18A2 gene in sporadic Parkinson's disease in Chinese Han population / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 825-828, 2015.
Artículo
en Inglés
| WPRIM | ID: wpr-815263
9.
L10P mutation in DJ-1 gene induced oxidative stress and mitochondrial disfunction / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 1285-1291, 2015.
Artículo
en Inglés
| WPRIM | ID: wpr-815339
10.
Expression profiles of genes in wild-type DJ-1 and A39S DJ-1 mutant cells / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 325-332, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-468163
11.
Establishment of transgenic mouse models expressing human HSP22 protein / 中华老年医学杂志
Chinese Journal of Geriatrics
; (12): 333-337, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-431187
12.
Mutation analysis of microRNA-7 gene in Chinese patients with Parkinson's disease / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 1189-1192, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-814611
13.
DJ-1 gene rearrangement mutation in patients with autosomal recessive early-onset parkinsonism using real-time PCR / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 438-444, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-814432
14.
Analyses of clinical and genetic characteristics of 179 patients with hereditary spastic paraplegia / 中华神经科杂志
Chinese Journal of Neurology
; (12): 681-685, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-386971
15.
Analysis of parkin gene mutations in Han Chinese with sporadic early-onset parkinsonism in southern China / 中华神经科杂志
Chinese Journal of Neurology
; (12): 692-696, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-386966
16.
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, 7, 8, 10, 12, 17 and dentatorubral-pallidoluysian atrophy in Chinese Han population / 中华神经科杂志
Chinese Journal of Neurology
; (12): 672-675, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-391953
17.
Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 620-625, 2009.
Artículo
en Zh
| WPRIM | ID: wpr-287364
18.
Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 511-514, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-308028
19.
Chronic nicotine induces the changes of locomotor activities in rats by increasing the mRNA levels of dopamine D1 receptor in striatum / 中国组织工程研究
Chinese Journal of Tissue Engineering Research
; (53): 189-192, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-408241
20.
Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 189-191, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-321130