1691 - 1700 of 8587 Results
Title
Year
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OPENTitle: A Genome‐Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6Journal Name: Annals of Human GeneticsPublisher: WileyVol: 75Issue #: 3Start Page: 351End Page: 358Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/j.1469-1809.2011.00643.xBest OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1469-1809.2011.00643.xCitation Count: 10
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OPENTitle: TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cordJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 128Issue #: 3Start Page: 423End Page: 437Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-014-1299-6Best OA location URL: http://doi.org/10.1007/s00401-014-1299-6Citation Count: 240
- TDP-43 deposition in prospectively followed, cognitively normal elderly individuals: correlation with argyrophilic grains but not other concomitant pathologies2013OPENTitle: TDP-43 deposition in prospectively followed, cognitively normal elderly individuals: correlation with argyrophilic grains but not other concomitant pathologiesJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 126Issue #: 1Start Page: 51End Page: 57Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-013-1110-0Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3691299Citation Count: 90
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OPENTitle: Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degenerationJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 127Issue #: 2Start Page: 271End Page: 282Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-013-1193-7Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3943649Citation Count: 77
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OPENTitle: Heterogeneous neuropathological findings in Parkinson’s disease with mild cognitive impairmentJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 120Issue #: 6Start Page: 827End Page: 828Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-010-0744-4Best OA location URL: https://europepmc.org/articles/pmc3100801?pdf=renderCitation Count: 84
- Next-generation active immunization approach for synucleinopathies: implications for Parkinson’s disease clinical trials2014OPENTitle: Next-generation active immunization approach for synucleinopathies: implications for Parkinson’s disease clinical trialsJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 127Issue #: 6Start Page: 861End Page: 879Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-014-1256-4Citation Count: 216
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OPENTitle: VPS35 Mutations in Parkinson DiseaseJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 89Issue #: 1Start Page: 162End Page: 167Publication Date:Open Access(OA) Status: OPENLicense: other-oaDOI - Digital Object Identifier: 10.1016/j.ajhg.2011.06.001Best OA location URL: http://www.cell.com/article/S0002929711002424/pdfCitation Count: 835
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OPENTitle: High-Resolution Whole-Genome Association Study of Parkinson DiseaseJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 77Issue #: 5Start Page: 685End Page: 693Publication Date:Open Access(OA) Status: OPENLicense: publisher-specific-oaDOI - Digital Object Identifier: 10.1086/496902Best OA location URL: http://www.cell.com/article/S0002929707633540/pdfCitation Count: 510
- LRRK2 G2019S in Families with Parkinson Disease Who Originated from Europe and the Middle East: Evidence of Two Distinct Founding Events Beginning Two Millennia Ago2006OPENTitle: LRRK2 G2019S in Families with Parkinson Disease Who Originated from Europe and the Middle East: Evidence of Two Distinct Founding Events Beginning Two Millennia AgoJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 79Issue #: 4Start Page: 752End Page: 758Publication Date:Open Access(OA) Status: OPENLicense: other-oaDOI - Digital Object Identifier: 10.1086/508025Best OA location URL: http://www.cell.com/article/S0002929707630870/pdfCitation Count: 120
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OPENTitle: Association of Parkinson Disease with Structural and Regulatory Variants in the HLA RegionJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 93Issue #: 5Start Page: 984End Page: 993Publication Date:Open Access(OA) Status: OPENLicense: publisher-specific-oaDOI - Digital Object Identifier: 10.1016/j.ajhg.2013.10.009Best OA location URL: http://www.cell.com/article/S0002929713004667/pdfCitation Count: 167