6651 - 6660 of 7939 Results
Title
Year
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RESTRICTEDTitle: The emerging role of SMPD1 mutations in Parkinson's disease: Implications for future studiesJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 21Issue #: 10Start Page: 1294End Page: 1295Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2015.08.018Citation Count: 35
- Immune phenotypes of microglia in human neurodegenerative disease: challenges to detecting microglial polarization in human brains2015RESTRICTEDTitle: Immune phenotypes of microglia in human neurodegenerative disease: challenges to detecting microglial polarization in human brainsJournal Name: Alzheimer's Research & TherapyPublisher: Springer Science and Business Media LLCVol: 7Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13195-015-0139-9Best OA location URL: https://alzres.biomedcentral.com/counter/pdf/10.1186/s13195-015-0139-9Citation Count: 391
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OPENTitle: Neuropathological comparisons of amnestic and nonamnestic mild cognitive impairmentJournal Name: BMC NeurologyPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12883-015-0403-4Best OA location URL: https://bmcneurol.biomedcentral.com/counter/pdf/10.1186/s12883-015-0403-4Citation Count: 42
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RESTRICTEDTitle: Genome-wide variant by serum urate interaction in Parkinson's diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 78Issue #: 5Start Page: 731End Page: 741Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.24504Citation Count: 10
- Increased central microglial activation associated with peripheral cytokine levels in premanifest Huntington's disease gene carriers2015RESTRICTEDTitle: Increased central microglial activation associated with peripheral cytokine levels in premanifest Huntington's disease gene carriersJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 83Issue #:Start Page: 115End Page: 121Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.nbd.2015.08.011Citation Count: 131
- Reaction-Based “Off–On” Fluorescent Probe Enabling Detection of Endogenous Labile Fe2+ and Imaging of Zn2+-induced Fe2+ Flux in Living Cells and Elevated Fe2+ in Ischemic Stroke2015RESTRICTEDTitle: Reaction-Based “Off–On” Fluorescent Probe Enabling Detection of Endogenous Labile Fe2+ and Imaging of Zn2+-induced Fe2+ Flux in Living Cells and Elevated Fe2+ in Ischemic StrokeJournal Name: Bioconjugate ChemistryPublisher: American Chemical Society (ACS)Vol: 27Issue #: 2Start Page: 302End Page: 308Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1021/acs.bioconjchem.5b00259Citation Count: 65
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OPENTitle: Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)Journal Name: Movement DisordersPublisher: WileyVol: 31Issue #: 1Start Page: 79End Page: 85Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.26374Best OA location URL: https://europepmc.org/articles/pmc4724309?pdf=renderCitation Count: 67
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RESTRICTEDTitle: Clinical and imaging markers in premotor LRRK2 G2019S mutation carriersJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 21Issue #: 10Start Page: 1170End Page: 1176Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2015.08.007Citation Count: 36
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RESTRICTEDTitle: Active immunization therapies for Parkinson's disease and multiple system atrophyJournal Name: Movement DisordersPublisher: WileyVol: 31Issue #: 2Start Page: 214End Page: 224Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.26377Citation Count: 68
- Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study2015OPENTitle: Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 14Issue #: 10Start Page: 1002End Page: 1009Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(15)00178-7Best OA location URL: https://escholarship.org/content/qt9nf852rq/qt9nf852rq.pdf?t=ntzu2fCitation Count: 187