NeuralCipher Source record
LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi Jews.
DOI: 10.1159/000447450PMID: 27449028
A bibliographic record traceable to Europe PMC.
404 articles found
“Parkinson GBA” Clear search
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Derivation, Characterization, and Neural Differentiation of Integration-Free Induced Pluripotent Stem Cell Lines from Parkinson's Disease Patients Carrying SNCA, LRRK2, PARK2, and GBA Mutations.
DOI: 10.1371/journal.pone.0154890PMID: 27191603
A bibliographic record traceable to Europe PMC.
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The contribution of mutant GBA to the development of Parkinson disease in Drosophila.
DOI: 10.1093/hmg/ddw129PMID: 27162249
A bibliographic record traceable to Europe PMC.
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The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients.
DOI: 10.1016/j.neulet.2016.04.014PMID: 27085534
A bibliographic record traceable to Europe PMC.
Open access
ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons.
DOI: 10.1016/j.stemcr.2016.01.013PMID: 26905200
A bibliographic record traceable to Europe PMC.
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Glucocerebrosidase enzyme activity in GBA mutation Parkinson's disease.
DOI: 10.1016/j.jocn.2015.12.004PMID: 26857292
A bibliographic record traceable to Europe PMC.
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Clinical studies of GBA1-associated parkinsonism: progress and challenges.
DOI: 10.2217/nmt.15.68PMID: 26782311
A bibliographic record traceable to Europe PMC.
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Advances in GBA-associated Parkinson's disease--Pathology, presentation and therapies.
DOI: 10.1016/j.neuint.2015.12.004PMID: 26743617
A bibliographic record traceable to Europe PMC.
Open access
Endoplasmic reticulum and lysosomal Ca²⁺ stores are remodelled in GBA1-linked Parkinson disease patient fibroblasts.
DOI: 10.1016/j.ceca.2015.11.002PMID: 26691915
A bibliographic record traceable to Europe PMC.
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GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?
DOI: 10.1111/ene.12894PMID: 26549049
A bibliographic record traceable to Europe PMC.
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An assessment of the frequency of mutations in the GBA and VPS35 genes in Hungarian patients with sporadic Parkinson's disease.
DOI: 10.1016/j.neulet.2015.11.001PMID: 26547032
A bibliographic record traceable to Europe PMC.
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Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression.
DOI: 10.1016/j.neurobiolaging.2015.09.014PMID: 26601739
A bibliographic record traceable to Europe PMC.
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