about
Validity and reliability testing of the Chinese (mainland) version of the 39-item Parkinson's Disease Questionnaire (PDQ-39).Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literature.Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.Abnormal baseline brain activity in Parkinson's disease with and without REM sleep behavior disorder: A resting-state functional MRI study.A clinical study of the coronal plane deformity in Parkinson disease.Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.Influence of regional iron on the motor impairments of Parkinson's disease: A quantitative susceptibility mapping study.Regionally progressive accumulation of iron in Parkinson's disease as measured by quantitative susceptibility mapping.Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.L-3-n-Butylphthalide Protects HSPB8 K141N Mutation-Induced Oxidative Stress by Modulating the Mitochondrial Apoptotic and Nrf2 Pathways.Greater loss of white matter integrity in postural instability and gait difficulty subtype of Parkinson's disease.Huntington's Disease presenting with chorea of the ears.[Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update].Prevalence and clinical correlation of dysphagia in Parkinson disease: a study on Chinese patients.Cortical abnormalities in Parkinson's disease patients and relationship to depression: A surface-based morphometry study.Altered brain network centrality in depressed Parkinson's disease patients.Abnormal amygdala function in Parkinson's disease patients and its relationship to depression.Different patterns of gray matter density in early- and middle-late-onset Parkinson's disease: a voxel-based morphometry study.Disrupted white matter integrity in depressed versus non-depressed Parkinson's disease patients: a tract-based spatial statistics study.[Analysis of clinical phenotype and CGH1 gene mutations in a family affected with dopa-responsive dystonia].Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.[Familial cortical myoclonic tremor with epilepsy in a pedigree].Dramatic response to pyridoxine in a girl with absence epilepsy with ataxia caused by a de novo CACNA1A mutation.Genetic analysis of the TMEM230 gene in Chinese patients with familial Parkinson disease.Cervical spinal cord compression caused by X-linked hypophosphatemic rickets with a novel PHEX mutation.A Novel Homozygous Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic ParaplegiaLRP10 in autosomal-dominant Parkinson's diseaseEvaluation of MYORG mutations as a novel cause of primary familial brain calcification[Clinical, pathological and genetic studies in a Chinese Charcot-Marie-Tooth disease type 2 family]Spinal muscular atrophy combined with sporadic olivopontocerebellar atrophyFamilial recurrent Bell's palsyMutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in ChinaStudy of methylation levels of parkin gene promoter in Parkinson's disease patientsSerum urate and the risk of Parkinson's disease: results from a meta-analysisNovel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysisGenetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegiaHomozygous p.D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism: further evidence of a fourth phenotype of PLA2G6-associated neurodegeneration[Genetic and clinical analysis in a Parkinson's disease family caused by expansion of SCA2]
P50
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P50
description
researcher ORCID ID=0000-0001-6951-7698
@en
name
Wei Luo
@ast
Wei Luo
@en
Wei Luo
@nl
type
label
Wei Luo
@ast
Wei Luo
@en
Wei Luo
@nl
prefLabel
Wei Luo
@ast
Wei Luo
@en
Wei Luo
@nl
P106
P31
P496
0000-0001-6951-7698