相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。The genetic architecture of Parkinson's disease
Cornelis Blauwendraat et al.
LANCET NEUROLOGY (2020)
Whole-exome sequencing in early-onset Parkinson's disease among ethnic Chinese
Nannan Li et al.
NEUROBIOLOGY OF AGING (2020)
Neuroinflammation in Neurodegenerative Diseases: Current Multi-modal Imaging Studies and Future Opportunities for Hybrid PET/MRI
Marco Aiello et al.
NEUROSCIENCE (2019)
A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing
Chin-Hsien Lin et al.
MOVEMENT DISORDERS (2019)
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study
Manuela M. X. Tan et al.
BRAIN (2019)
The interplay of aging, genetics and environmental factors in the pathogenesis of Parkinson's disease
Shirley Yin-Yu Pang et al.
TRANSLATIONAL NEURODEGENERATION (2019)
Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort
Nannan Yang et al.
NEUROBIOLOGY OF AGING (2019)
Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study
Naveed Malek et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)
Targeted Therapies for Parkinson's Disease: From Genetics to the Clinic
S. Pablo Sardi et al.
MOVEMENT DISORDERS (2018)
Genetic analysis of LRRK2 in Parkinson's disease in Han Chinese population
Jin-Ru Zhang et al.
NEUROBIOLOGY OF AGING (2018)
Cellular and Molecular Basis of Neurodegeneration in Parkinson Disease
Xian-Si Zeng et al.
FRONTIERS IN AGING NEUROSCIENCE (2018)
The genetic landscape of Parkinson's disease
A. Lunati et al.
REVUE NEUROLOGIQUE (2018)
The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review
Fang Peng et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2017)
Homozygous alpha-synuclein p.A53V in familial Parkinson's disease
Hiroyo Yoshino et al.
NEUROBIOLOGY OF AGING (2017)
A dose effect of mutations in the GBA gene on Parkinson's disease phenotype
Avner Thaler et al.
PARKINSONISM & RELATED DISORDERS (2017)
Early-onset vs. Late-onset Parkinson's disease: A Clinical-pathological Study
Leslie Wayne Ferguson et al.
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES (2016)
Association Tests for Rare Variants
Dan L. Nicolae
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 17 (2016)
The heterozygous A53T mutation in the alpha-synuclein gene in a Chinese Han patient with Parkinson disease: case report and literature review
Wei-Xi Xiong et al.
JOURNAL OF NEUROLOGY (2016)
Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease
Marie Y. Davis et al.
JAMA NEUROLOGY (2016)
MDS clinical diagnostic criteria for Parkinson's disease
Ronald B. Postuma et al.
MOVEMENT DISORDERS (2015)
Mechanisms of Alpha-Synuclein Action on Neurotransmission: Cell-Autonomous and Non-Cell Autonomous Role
Marco Emanuele et al.
BIOMOLECULES (2015)
Genetic assessment of familial and early-onset Parkinson's disease in a Greek population
M. Bozi et al.
EUROPEAN JOURNAL OF NEUROLOGY (2014)
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations
Jia Nee Foo et al.
HUMAN MOLECULAR GENETICS (2014)
The link between the GBA gene and parkinsonism
Ellen Sidransky et al.
LANCET NEUROLOGY (2012)
The Motor Phenotype of Parkinson's Disease in Relation to Age at Onset
Mirdhu M. Wickremaratchi et al.
MOVEMENT DISORDERS (2011)
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease
S. Lesage et al.
JOURNAL OF MEDICAL GENETICS (2009)
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
K. Haugarvoll et al.
NEUROLOGY (2008)
Epidemiology of Parkinson's disease
Lonneke M. L. de Lau et al.
LANCET NEUROLOGY (2006)
Lrrk2 pathogenic substitutions in Parkinson's disease
IF Mata et al.
NEUROGENETICS (2005)
Early-onset parkinsonism associated with PINK1 mutations -: Frequency, genotypes, and phenotypes
V Bonifati et al.
NEUROLOGY (2005)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
Evita Evangelia Christou et al.
SEMINARS IN OPHTHALMOLOGY
分享论文
