6471 - 6480 of 8761 Results
Title
Year
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OPENTitle: Metabolic network expression in parkinsonism: Clinical and dopaminergic correlationsJournal Name: Journal of Cerebral Blood Flow & MetabolismPublisher: SAGE PublicationsVol: 37Issue #: 2Start Page: 683End Page: 693Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1177/0271678x16637880Best OA location URL: https://journals.sagepub.com/doi/pdf/10.1177/0271678X16637880Citation Count: 58
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OPENTitle: Binding to serine 65‐phosphorylated ubiquitin primes Parkin for optimal PINK 1‐dependent phosphorylation and activationJournal Name: EMBO reportsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 8Start Page: 939End Page: 954Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/embr.201540352Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/embr.201540352Citation Count: 230
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OPENTitle: Indirect tolerability comparison of Deutetrabenazine and Tetrabenazine for Huntington diseaseJournal Name: Journal of Clinical Movement DisordersPublisher: Springer Science and Business Media LLCVol: 4Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s40734-017-0051-5Best OA location URL: https://clinicalmovementdisorders.biomedcentral.com/track/pdf/10.1186/s40734-017-0051-5Citation Count: 87
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OPENTitle: Quantifying physical decline in juvenile neuronal ceroid lipofuscinosis (Batten disease)Journal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 77Issue #: 20Start Page: 1801End Page: 1807Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e318237f649Best OA location URL: https://n.neurology.org/content/neurology/77/20/1801.full.pdfCitation Count: 56
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OPENTitle: TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTDJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 21Issue #: 2Start Page: 228End Page: 239Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41593-017-0047-3Best OA location URL: https://www.nature.com/articles/s41593-017-0047-3.pdfCitation Count: 527
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OPENTitle: GFAP mutations, age at onset, and clinical subtypes in Alexander diseaseJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 77Issue #: 13Start Page: 1287End Page: 1294Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e3182309f72Best OA location URL: https://n.neurology.org/content/neurology/77/13/1287.full.pdfCitation Count: 230
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OPENTitle: Murine models of acute neuronopathic Gaucher diseaseJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 104Issue #: 44Start Page: 17483End Page: 17488Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1073/pnas.0708086104Citation Count: 188
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OPENTitle: TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 76Issue #: 5Start Page: 467End Page: 474Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820a0e3bBest OA location URL: https://n.neurology.org/content/neurology/76/5/467.full.pdfCitation Count: 235
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions2010OPENTitle: Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 42Issue #: 3Start Page: 234End Page: 239Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/ng.536Best OA location URL: https://research.vu.nl/en/publications/84f83b44-8218-449b-8492-6fc07730d692Citation Count: 567
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OPENTitle: NEDD4-mediated HSF1 degradation underlies α-synucleinopathyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 25Issue #: 2Start Page: 211End Page: 222Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddv445Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/2/211/18526601/ddv445.pdfCitation Count: 84