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Alterations in intrinsic functional networks in Parkinson’s disease patients with depression: A resting‐state functional magnetic resonance imaging study

CNS neuroscience & therapeutics, 2021-03, Vol.27 (3), p.289-298

2021

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Clinical outcomes and predictive model of platelet reactivity to clopidogrel after acute ischemic vascular events

Chinese medical journal, 2019-05, Vol.132 (9), p.1053-1062

2019

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Non-prescription cold and flu medication-induced transient myopia with uveal effusion: case report

BMC ophthalmology, 2019-06, Vol.19 (1), p.136-136, Article 136

2019

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Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism

Movement disorders, 2008-10, Vol.23 (14), p.2074-2079

2008

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Idiopathic Basal Ganglia Calcification Presented with Progressive Supranuclear Palsy-like Features

Chinese medical journal, 2016-02, Vol.129 (4), p.478-479

2016

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The putaminal abnormalities on 3.0T magnetic resonance imaging: can they separate parkinsonism-predominant multiple system atrophy from Parkinson's disease?

Acta radiologica (1987), 2015-03, Vol.56 (3), p.322-328

2015

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Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort

Neurobiology of aging, 2014-07, Vol.35 (7), p.1780.e11-1780.e12

2014

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RIT2 polymorphism is associated with Parkinson's disease in a Han Chinese population

Neurobiology of aging, 2015-03, Vol.36 (3), p.1603.e15-1603.e17

2015

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Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration

Movement disorders, 2005-07, Vol.20 (7), p.819-821

2005

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Roles of microRNAs in immunopathogenesis of non-alcoholic fatty liver disease revealed by integrated analysis of microRNA and mRNA expression profiles

Hepatobiliary & pancreatic diseases international, 2017-02, Vol.16 (1), p.65-79

2017

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The pleiotropic ABNORMAL FLOWER AND DWARF1 affects plant height, floral development and grain yield in rice

Journal of integrative plant biology, 2016-06, Vol.58 (6), p.529-539

2016

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DOPAMINE D4 RECEPTOR GENE EXON III POLYMORPHISM AND INTERINDIVIDUAL VARIATION IN RESPONSE TO CLOZAPINE

International journal of neuroscience, 2005-11, Vol.115 (11), p.1539-1547

2005

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Phytochemical investigation on Lysimachia fortunei

Zhongguo zhongyao zazhi, 2007-04, Vol.32 (7), p.596

2007

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Mutation analysis of GCH1 gene in Chinese patients with dopa responsive dystonia

Zhonghua yi xue yi chuan xue za zhi, 2007-06, Vol.24 (3), p.302

2007

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Genetic lineage tracing identifies in situ Kit-expressing cardiomyocytes

Cell research, 2016-01, Vol.26 (1), p.119-130

2016

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Abundance and Fluorescent Components of Dissolved Organic Matter Affected by Land Use in a Drinking Water Source

Huanjing kexue, 2022-04, Vol.43 (4), p.1950

2022

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Research on screening and identification of proteins interacting with ataxin-3

Zhonghua yi xue yi chuan xue za zhi, 2005-06, Vol.22 (3), p.242

2005

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Mutation detection of parkin gene by denaturing high performance liquid chromatography

Zhonghua yi xue yi chuan xue za zhi, 2007-08, Vol.24 (4), p.449

2007

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Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR

Zhong hua yi xue za zhi, 2006-06, Vol.86 (21), p.1447-1449

2006

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Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6

Zhong hua yi xue za zhi, 2005-06, Vol.85 (22), p.1538-1541

2005

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Distribution of genotype and allele frequencies of dopamine D4 receptor gene 48 bp variable number tandem repeat polymorphism in Chinese Han population in Hunan

Zhonghua yi xue yi chuan xue za zhi, 2005-08, Vol.22 (4), p.470

2005

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ASSOCIATION ANALYSIS OF SEROTONIN TRANSPORTER PROMOTER GENE POLYMORPHISM WITH ADHD AND RELATED SYMPTOMATOLOGY

International journal of neuroscience, 2005-08, Vol.115 (8), p.1183-1191

2005

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Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism

Zhonghua yi xue yi chuan xue za zhi, 2005-12, Vol.22 (6), p.641

2005

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Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism

Zhonghua yi xue yi chuan xue za zhi, 2006-02, Vol.23 (1), p.70

2006

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The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family

Chung-hua nei kʿo tsa chih, 2005-05, Vol.44 (5), p.360

2005

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Alterations in intrinsic functional networks in Parkinson’s disease patients with depression: A resting‐state functional magnetic resonance imaging study

Clinical outcomes and predictive model of platelet reactivity to clopidogrel after acute ischemic vascular events

Non-prescription cold and flu medication-induced transient myopia with uveal effusion: case report

Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism

Idiopathic Basal Ganglia Calcification Presented with Progressive Supranuclear Palsy-like Features

The putaminal abnormalities on 3.0T magnetic resonance imaging: can they separate parkinsonism-predominant multiple system atrophy from Parkinson's disease?

Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort

RIT2 polymorphism is associated with Parkinson's disease in a Han Chinese population

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration

Roles of microRNAs in immunopathogenesis of non-alcoholic fatty liver disease revealed by integrated analysis of microRNA and mRNA expression profiles

The pleiotropic ABNORMAL FLOWER AND DWARF1 affects plant height, floral development and grain yield in rice

DOPAMINE D4 RECEPTOR GENE EXON III POLYMORPHISM AND INTERINDIVIDUAL VARIATION IN RESPONSE TO CLOZAPINE

Phytochemical investigation on Lysimachia fortunei

Mutation analysis of GCH1 gene in Chinese patients with dopa responsive dystonia

Genetic lineage tracing identifies in situ Kit-expressing cardiomyocytes

Abundance and Fluorescent Components of Dissolved Organic Matter Affected by Land Use in a Drinking Water Source

Research on screening and identification of proteins interacting with ataxin-3

Mutation detection of parkin gene by denaturing high performance liquid chromatography

Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR

Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6

Distribution of genotype and allele frequencies of dopamine D4 receptor gene 48 bp variable number tandem repeat polymorphism in Chinese Han population in Hunan

ASSOCIATION ANALYSIS OF SEROTONIN TRANSPORTER PROMOTER GENE POLYMORPHISM WITH ADHD AND RELATED SYMPTOMATOLOGY

Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism

Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism

The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family

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