6881 - 6890 of 8824 Results
Title
Year
-
OPENTitle: Shared mechanisms across the major psychiatric and neurodegenerative diseasesJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page: 4314End Page: 4314Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-022-31873-5Best OA location URL: https://escholarship.org/uc/item/23t9767xCitation Count: 181
-
OPENTitle: The safety/tolerability of opicapone when used early in Parkinson's disease patients with levodopa-induced motor fluctuations: A post-hoc analysis of BIPARK-I and IIJournal Name: Frontiers in NeurologyPublisher: Frontiers Media SAVol: 13Issue #:Start Page: 994114End Page: 994114Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fneur.2022.994114Best OA location URL: https://doi.org/10.3389/fneur.2022.994114Citation Count: 8
-
OPENTitle: Virtual house calls for Parkinson disease (Connect.Parkinson): study protocol for a randomized, controlled trialJournal Name: TrialsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 465End Page: 465Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1186/1745-6215-15-465Best OA location URL: https://trialsjournal.biomedcentral.com/counter/pdf/10.1186/1745-6215-15-465Citation Count: 28
-
OPENTitle: Comparison of Patient and Expert Perceptions of the Attainment of Research Milestones in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 1Start Page: 171End Page: 177Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/mds.28319Best OA location URL: https://movementdisorders.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28319Citation Count: 4
- Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases2016OPENTitle: Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPasesJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 5Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.7554/elife.12813Best OA location URL: https://doi.org/10.7554/elife.12813Citation Count: 1061
-
OPENTitle: Resting state functional MRI in Parkinson’s disease: the impact of deep brain stimulation on ‘effective’ connectivityJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 137Issue #: 4Start Page: 1130End Page: 1144Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awu027Best OA location URL: https://academic.oup.com/brain/article-pdf/137/4/1130/13799493/awu027.pdfCitation Count: 220
-
OPENTitle: Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disordersJournal Name: Genetics in MedicinePublisher: Elsevier BVVol: 26Issue #: 6Start Page: 101117End Page: 101117Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.gim.2024.101117Best OA location URL: https://doi.org/10.1016/j.gim.2024.101117Citation Count: 3
-
OPENTitle: Expanding the phenotype of PPP1R21‐related neurodevelopmental disorderJournal Name: Clinical GeneticsPublisher: WileyVol: 105Issue #: 6Start Page: 620End Page: 629Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/cge.14492Best OA location URL: https://pmc.ncbi.nlm.nih.gov/articles/PMC11065596/pdf/nihms-1961168.pdfCitation Count: 5
-
OPENTitle: Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamicsJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 5Start Page: 1751End Page: 1767Publication Date:Open Access(OA) Status: OPENLicense: public-domain, public-domainDOI - Digital Object Identifier: 10.1093/brain/awad427Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awad427/54752638/awad427.pdfCitation Count: 23
-
OPENTitle: Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcificationsJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 2269End Page: 2269Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41467-024-46354-0Best OA location URL: https://doi.org/10.1038/s41467-024-46354-0Citation Count: 42