1821 - 1830 of 6516 Results
Title
Year
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OPENTitle: Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Journal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 71Issue #:Start Page: 44End Page: 45Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.01.017Best OA location URL: http://www.prd-journal.com/article/S1353802020300237/pdfCitation Count: 8
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OPENTitle: Selective loss of glucocerebrosidase activity in sporadic Parkinson’s disease and dementia with Lewy bodiesJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 15End Page: 15Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1186/s13024-015-0010-2Best OA location URL: https://molecularneurodegeneration.biomedcentral.com/counter/pdf/10.1186/s13024-015-0010-2Citation Count: 145
- Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score2020OPENTitle: Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk ScoreJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 5Start Page: 774End Page: 780Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.27974Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8975556Citation Count: 86
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OPENTitle: Genetic impact on cognition and brain function in newly diagnosed Parkinson’s disease: ICICLE-PD studyJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 137Issue #: 10Start Page: 2743End Page: 2758Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awu201Best OA location URL: https://academic.oup.com/brain/article-pdf/137/10/2743/11140806/awu201.pdfCitation Count: 147
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OPENTitle: The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightJournal Name: Movement DisordersPublisher: WileyVol: 34Issue #: 12Start Page: 1851End Page: 1863Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.27864Best OA location URL: http://hdl.handle.net/10668/15500Citation Count: 70
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OPENTitle: Two-year clinical progression in focal and diffuse subtypes of Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page: 29End Page: 29Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-023-00466-4Best OA location URL: https://www.nature.com/articles/s41531-023-00466-4.pdfCitation Count: 34
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OPENTitle: Parkin coregulates glutathione metabolism in adult mammalian brainJournal Name: Acta Neuropathologica CommunicationsPublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 19End Page: 19Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s40478-022-01488-4Best OA location URL: https://actaneurocomms.biomedcentral.com/counter/pdf/10.1186/s40478-022-01488-4Citation Count: 14
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OPENTitle: GPNMB confers risk for Parkinson’s disease through interaction with α-synucleinJournal Name: SciencePublisher: American Association for the Advancement of Science (AAAS)Vol: 377Issue #: 6608Start Page: eabk0637End Page: eabk0637Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/science.abk0637Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9870036Citation Count: 144
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OPENTitle: Disease specific and nonspecific metabolic brain networks in behavioral variant of frontotemporal dementiaJournal Name: Human Brain MappingPublisher: WileyVol: 44Issue #: 3Start Page: 1079End Page: 1093Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/hbm.26140Best OA location URL: https://doi.org/10.1002/hbm.26140Citation Count: 13
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OPENTitle: The genetic regulation of protein expression in cerebrospinal fluidJournal Name: EMBO Molecular MedicinePublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: e16359End Page: e16359Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/emmm.202216359Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/emmm.202216359Citation Count: 53