Detalhe da pesquisa
1.
A novel tyrosine hydroxylase variant in a group of Chinese patients with dopa-responsive dystonia.
Int J Neurosci
; 127(8): 694-700, 2017 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-27619486
2.
Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.
Am J Med Genet B Neuropsychiatr Genet
; 168(7): 595-9, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26130016
3.
Mills' syndrome is a unique entity of upper motor neuron disease with N-shaped progression: Three case reports.
World J Clin Cases
; 10(19): 6664-6671, 2022 Jul 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35979278
4.
[Silver syndrome: report of a family with 5 cases].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(4): 500, 2013 Aug.
Artigo
Chinês
| MEDLINE | ID: mdl-23926023
5.
Congenital anomaly of the posterior arch of the atlas: a rare risk factor for posterior circulation stroke.
J Neurointerv Surg
; 9(7): e27, 2017 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-28082448
6.
Congenital anomaly of the posterior arch of the atlas: a rare risk factor for posterior circulation stroke.
BMJ Case Rep
; 20172017 Jan 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28052941
7.
Genetic profile of Chinese patients with Charcot-Marie-Tooth disease.
Chin Med J (Engl)
; 133(21): 2633-2634, 2020 Nov 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32941234
8.
Validity and reliability testing of the Chinese (mainland) version of the 39-item Parkinson's Disease Questionnaire (PDQ-39).
J Zhejiang Univ Sci B
; 11(7): 531-8, 2010 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-20593519