2181 - 2190 of 9104 Results
Title
Year
-
OPENTitle: In vivo dopaminergic and serotonergic dysfunction in DCTN1 gene mutation carriersJournal Name: Movement DisordersPublisher: WileyVol: 29Issue #: 9Start Page: 1197End Page: 1201Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.25893Best OA location URL: http://doi.org/10.1002/mds.25893Citation Count: 20
-
OPENTitle: ALS-FTD Complex Disorder due to <b><i>C9ORF72</i></b> Gene Mutation: Description of First Polish FamilyJournal Name: European NeurologyPublisher: S. Karger AGVol: 72Issue #: 1-2Start Page: 64End Page: 71Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1159/000362267Best OA location URL: https://karger.com/ene/article-pdf/72/1-2/64/2724525/000362267.pdfCitation Count: 1
- Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease2010OPENTitle: Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's diseaseJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 226Issue #: 1Start Page: 207End Page: 217Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2010.09.001Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3108022Citation Count: 58
-
OPENTitle: Loss of enteric dopaminergic neurons and associated changes in colon motility in an MPTP mouse model of Parkinson's diseaseJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 207Issue #: 1Start Page: 4End Page: 12Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2007.05.010Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/2277100Citation Count: 239
- Chronic deprivation of TrkB signaling leads to selective late-onset nigrostriatal dopaminergic degeneration2010RESTRICTEDTitle: Chronic deprivation of TrkB signaling leads to selective late-onset nigrostriatal dopaminergic degenerationJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 228Issue #: 1Start Page: 118End Page: 125Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2010.12.018Citation Count: 79
-
OPENTitle: The PET tracer [ 11 C]MODAG-005 targets alpha-synuclein aggregates in the brainJournal Name: Science Translational MedicinePublisher: American Association for the Advancement of Science (AAAS)Vol: 18Issue #: 851Start Page: eaec0813End Page: eaec0813Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/scitranslmed.aec0813Best OA location URL: https://pub.dzne.de/record/287436Citation Count: 0
-
OPENTitle: Cortico-Subthalamic Field Potentials Support Classification of the Natural Gait Cycle in Parkinson’s Disease and Reveal Individualized Spectral SignaturesJournal Name: eneuroPublisher: Society for NeuroscienceVol: 9Issue #: 6Start Page: ENEURO.0325End Page: 22.2022Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1523/eneuro.0325-22.2022Best OA location URL: https://www.eneuro.org/content/eneuro/9/6/ENEURO.0325-22.2022.full.pdfCitation Count: 29
-
OPENTitle: Intronic Haplotypes in GBA Modify Age at Diagnosis of Parkinson's: Replication in a SubgroupJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 6Start Page: 1468End Page: 1470Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28620Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28620Citation Count: 2
-
OPENTitle: A study of RNA splicing and protein expression in the living human brainJournal Name: PLOS OnePublisher: Public Library of Science (PLoS)Vol: 20Issue #: 10Start Page: e0332651End Page: e0332651Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0332651Best OA location URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0332651&type=printableCitation Count: 1
- A novel homozygous SQSTM1 frameshift variant in a Filipino adolescent with childhood-onset ataxia and gaze palsy2026RESTRICTEDTitle: A novel homozygous SQSTM1 frameshift variant in a Filipino adolescent with childhood-onset ataxia and gaze palsyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol:Issue #:Start Page: 108233End Page: 108233Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2026.108233Citation Count: 1