2951 - 2960 of 8620 Results
Title
Year
- Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases2015OPENTitle: Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 38Issue #:Start Page: 214.e7End Page: 214.e10Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2015.10.028Best OA location URL: https://doi.org/10.1016/j.neurobiolaging.2015.10.028Citation Count: 87
- Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease2013OPENTitle: Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 34Issue #: 8Start Page: 2077.e11End Page: 2077.e18Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2013.02.016Best OA location URL: http://doi.org/10.1016/j.neurobiolaging.2013.02.016Citation Count: 140
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OPENTitle: Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansionsJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 36Issue #: 2Start Page: 1223.e1End Page: 1223.e2Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2014.08.033Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4315721Citation Count: 30
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OPENTitle: Mutational analysis of parkin and PINK1 in multiple system atrophyJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 32Issue #: 3Start Page: 548.e5End Page: 548.e7Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2009.11.020Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3934211Citation Count: 21
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OPENTitle: Microglial responses to dopamine in a cell culture model of Parkinson's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 30Issue #: 11Start Page: 1805End Page: 1817Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2008.01.001Citation Count: 109
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OPENTitle: MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophyJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 76Issue #: 7Start Page: 670End Page: 672Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820c30c1Best OA location URL: http://n.neurology.org/content/neurology/76/7/670.full.pdfCitation Count: 72
- Aberrant intracellular localization of H3k4me3 demonstrates an early epigenetic phenomenon in Alzheimer's disease2015OPENTitle: Aberrant intracellular localization of H3k4me3 demonstrates an early epigenetic phenomenon in Alzheimer's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 36Issue #: 12Start Page: 3121End Page: 3129Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2015.08.017Best OA location URL: http://doi.org/10.1016/j.neurobiolaging.2015.08.017Citation Count: 54
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OPENTitle: Quantitative EEG as a predictive biomarker for Parkinson disease dementiaJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 77Issue #: 2Start Page: 118End Page: 124Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e318224af8dBest OA location URL: https://n.neurology.org/content/neurology/77/2/118.full.pdfCitation Count: 201
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OPENTitle: Olfaction in Parkin heterozygotes and compound heterozygotesJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 76Issue #: 4Start Page: 319End Page: 326Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e31820882aaBest OA location URL: https://n.neurology.org/content/neurology/76/4/319.full.pdfCitation Count: 48
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OPENTitle: Olfactory dysfunction in LRRK2 G2019S mutation carriersJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 77Issue #: 4Start Page: 319End Page: 324Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e318227041cBest OA location URL: https://n.neurology.org/content/neurology/77/4/319.full.pdfCitation Count: 62