Detalhe da pesquisa
1.
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.
Am J Hum Genet
; 105(1): 166-176, 2019 07 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31178126
2.
ABCC2 rs2273697 is associated with valproic acid concentrations in patients with epilepsy on valproic acid monotherapy.
Pharmazie
; 73(5): 279-282, 2018 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29724294
3.
[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L].
Zhonghua Yi Xue Za Zhi
; 92(7): 496-8, 2012 Feb 21.
Artigo
Chinês
| MEDLINE | ID: mdl-22490975
4.
Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study.
Neural Regen Res
; 17(3): 682-689, 2022 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-34380910
5.
Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer's disease.
Front Aging Neurosci
; 14: 906519, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35966797
6.
The Protective Effects of Osteocyte-Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with Aging.
Adv Sci (Weinh)
; 9(17): e2105316, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35508803
7.
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
Brain
; 133(Pt 12): 3510-8, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21106500
8.
Improving the diagnosis of AUS/FLUS thyroid nodules using an algorithm with combination of BRAFV600E mutation analysis and ultrasound pattern-based risk stratification.
Clin Hemorheol Microcirc
; 77(3): 273-285, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33185592
9.
[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
Chinês
| MEDLINE | ID: mdl-20931525
10.
Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature.
Front Neurol
; 11: 284, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32477232
11.
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.
J Neurol Sci
; 275(1-2): 92-9, 2008 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18835492
12.
[The advances in research on phosphorylation of polyglutamine disease].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 25(4): 414-7, 2008 Aug.
Artigo
Chinês
| MEDLINE | ID: mdl-18683139
13.
Multinodule abnormalities of the tracheobronchus: bronchoscopy findings and clinical diagnosis.
Clin Respir J
; 11(4): 440-447, 2017 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-26260022
14.
Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.
J Genet
; 87(3): 283-6, 2008 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19147916
15.
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China.
Front Cell Neurosci
; 7: 164, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-24068985
16.
SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.
PLoS One
; 8(1): e54214, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-23382880
17.
Inclusion interaction of chloramphenicol and heptakis (2,6-di-O-methyl)-ß-cyclodextrin: phase solubility and spectroscopic methods.
Spectrochim Acta A Mol Biomol Spectrosc
; 83(1): 570-4, 2011 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21945123