筛选条件 共查询到199条结果
排序方式
Increased Accumulation of alpha-Synuclein in Inflamed Appendices of Parkinson's Disease Patients

期刊: MOVEMENT DISORDERS, 2021; 36 (8)

Background The accumulation of alpha-synuclein (alpha-Syn) aggregates that leads to the onset of Parkinson's disease (PD) has been postulated to begin......

Higher Concentration of Plasma Glial Fibrillary Acidic Protein in Wilson Disease Patients With Neurological Manifestations

期刊: MOVEMENT DISORDERS, 2021; 36 (6)

Background Wilson disease is a rare, disabling, neurological genetic disease. Biomarkers of brain damage are less well developed. Objective The aim of......

Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource

期刊: MOVEMENT DISORDERS, 2021; 36 (8)

Background Whole-genome sequencing data are available from several large studies across a variety of diseases and traits. However, massive storage and......

Dynamics of Top-Down Control and Motor Networks in Parkinson's Disease

期刊: MOVEMENT DISORDERS, ; ()

Background: Motor symptoms in Parkinson's disease (PD) patients might be related to high-level task-control deficits. We aimed at investigating the dy......

Involvement of Autophagy in Levodopa-Induced Dyskinesia

期刊: MOVEMENT DISORDERS, ; ()

Background Autophagy is intensively studied in cancer, metabolic and neurodegenerative diseases, but little is known about its role in pathological co......

Lateralized Effect of Thalamic Deep Brain Stimulation Location on Verbal Abstraction

期刊: MOVEMENT DISORDERS, ; ()

Background Regionalized thalamic activity has been implicated in language function, and yet the effect of thalamic deep brain stimulation (DBS) on lan......

Decreased Penetrance of Parkinson's Disease in Elderly Carriers of Glucocerebrosidase Gene L444P/R Mutations: A Community-Based 10-Year Longitudinal Study

期刊: MOVEMENT DISORDERS, 2020; 35 (4)

Background Heterozygous mutations in the glucocerebrosidase gene (GBA) have been shown to be an important genetic risk factor for Parkinson's disease ......

MYORG mutation heterozygosity is associated with brain calcification

期刊: MOVEMENT DISORDERS, 2020; 35 (4)

Background Biallelic mutations in the MYORG gene were first identified as the cause of recessively inherited primary familial brain calcification. Int......

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

期刊: MOVEMENT DISORDERS, 2020; 35 (8)

Background Paroxysmal kinesigenic dyskinesia is a spectrum of involuntary dyskinetic disorders with high clinical and genetic heterogeneity. Mutations......

Magnetic Resonance Imaging and Neurofilament Light in the Differentiation of Parkinsonism

期刊: MOVEMENT DISORDERS, 2020; 35 (8)

Objective Accurate diagnosis is particularly challenging in Parkinson's disease (PD), multiple system atrophy (MSAp), and progressive supranuclear pal......

共199条页码: 1/14页15条/页