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1.
Genotype-phenotype characteristics and baseline natural history of Chinese myelin protein zero gene related neuropathy patients.
Eur J Neurol
; 30(4): 1069-1079, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36692866
2.
Clinical and genetic features of Charcot-Marie-Tooth disease patients with IGHMBP2 mutations.
Neuromuscul Disord
; 32(7): 564-571, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35660062
3.
Establishment and practice of the collaborative innovation system of the national clinical research center for geriatric disorders / 中华医院管理杂志
Chinese Journal of Hospital Administration
; (12): 482-485, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-958816
4.
Advances in the TAF1 gene / 中华神经科杂志
Chinese Journal of Neurology
; (12): 967-972, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-911823
5.
Research progress on the association between Parkinson′s disease and inflammatory bowel disease in genetics and gut microbiota / 中华神经科杂志
Chinese Journal of Neurology
; (12): 734-742, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-911786
6.
Research advances in clinical scales for essential tremor / 中华老年医学杂志
Chinese Journal of Geriatrics
; (12): 1458-1462, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-911038
7.
Research advances in the treatment of essential tremor / 中华神经科杂志
Chinese Journal of Neurology
; (12): 404-408, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-885436
8.
Research progress of somatosensory involvement in amyotrophic lateral sclerosis / 中华神经科杂志
Chinese Journal of Neurology
; (12): 296-302, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-885420
9.
Effect of CAG repeats on the age at onset of patients with spinocerebellar ataxia type 2 in China / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 793-799, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-907709
10.
The phenotypic and genetic spectrum of colony-stimulating factor 1 receptor gene-related leukoencephalopathy in China / 中华神经科杂志
Chinese Journal of Neurology
; (12): 1109-1118, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-911843
11.
Pay attention to repeat expansion mutation related neurogenetic diseases / 中华神经科杂志
Chinese Journal of Neurology
; (12): 161-165, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870793
12.
Advances in research on myoclonus-dystonia syndrome / 中华神经科杂志
Chinese Journal of Neurology
; (12): 552-558, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870848
13.
Mechanism of re-emergent tremor in Parkinson′s disease / 中华神经科杂志
Chinese Journal of Neurology
; (12): 544-547, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870841
14.
Clinical, pathologic and genetic analysis of 3 families with dystrophinopathy / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 1499-1502, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-864254
15.
Expert consensus on the management strategy of patients with hereditary ataxia during prevention and control of novel coronavirus pneumonia epidemic / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 359-366, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-828323
16.
Genetic and clinical features of sorbitol dehydrogenase gene-related Charcot-Marie-Tooth disease in Chinese population / 中华神经科杂志
Chinese Journal of Neurology
; (12): 882-887, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-870910
17.
A review on evaluating application of abnormal iron deposition in brain on diagnosis and differential diagnosis of Parkinson's disease / 中华老年医学杂志
Chinese Journal of Geriatrics
; (12): 594-600, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-745566
18.
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
19.
The electrophysiological characteristics of the four most common genotypes of Charcot-Marie-Tooth disease / 中华神经科杂志
Chinese Journal of Neurology
; (12): 26-33, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-734885
20.
Attach importance to the comorbidities of Parkinson's disease / 中国医师杂志
Journal of Chinese Physician
; (12): 1-5, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-705767