Differential effects of severe vs mild GBA mutations on Parkinson disease. - Wikidata - wikimedia - TriplyDB

Differential effects of severe vs mild GBA mutations on Parkinson disease.

Differential effects of severe vs mild GBA mutations on Parkinson disease.

http://www.wikidata.org/entity/Q35153677

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Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease Gaucher disease and comorbidities: B-cell malignancy and parkinsonism Modelling idiopathic Parkinson disease as a complex illness can inform incidence rate in healthy adults: the PREDIGT score Glucocerebrosidase modulates cognitive and motor activities in murine models of Parkinson's disease.GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.A Personalized Approach to Parkinson's Disease Patients Based on Founder Mutation Analysis Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden.GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis.Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's.A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers.Gaucher disease: Progress and ongoing challenges.The Complicated Relationship between Gaucher Disease and Parkinsonism: Insights from a Rare Disease.Glucocerebrosidase Mutations in Parkinson Disease.Survival and dementia in GBA-associated Parkinson's disease: The mutation matters.Mitochondria: A Common Target for Genetic Mutations and Environmental Toxicants in Parkinson's Disease.Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study.Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder.Lysosomal defects in ATP13A2 and GBA associated familial Parkinson's disease.Connecting Gaucher and Parkinson Disease: Considerations for Clinical and Research Genetic Counseling Settings.GBA Mutations Are Associated With Earlier Onset and Male Sex in Dementia With Lewy Bodies.The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease.Regional expression of genes mediating trans-synaptic alpha-synuclein transfer predicts regional atrophy in Parkinson disease.Self-report data as a tool for subtype identification in genetically-defined Parkinson's Disease

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P2860

Differential effects of severe vs mild GBA mutations on Parkinson disease.

http://www.wikidata.org/entity/Q35153677

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2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Differential effects of severe vs mild GBA mutations on Parkinson disease.

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Differential effects of severe vs mild GBA mutations on Parkinson disease.

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Differential effects of severe vs mild GBA mutations on Parkinson disease.

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Anat Mirelman

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Idan Amshalom

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Laura L Kilarski

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Mali Gana-Weisz

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P2860

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease

Clinical and genetic characteristics of Gaucher disease according to phenotypic subgroups.

Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.

The link between the GBA gene and parkinsonism

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews.

Mutations for Gaucher disease confer high susceptibility to Parkinson disease.

Parkinsonism associated with glucocerebrosidase mutation.

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