101 - 110 of 6420 Results
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Year
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OPENTitle: Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunitiesJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 112Issue #: 9Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.ajhg.2025.07.014Best OA location URL: https://www.cell.com/ajhg/pdf/S0002-9297(25)00284-8.pdfCitation Count: 0
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OPENTitle: Harmonization of CSF and imaging biomarkers in Alzheimer's disease: Need and practical applications for genetics studies and preclinical classificationJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 190Issue #:Start Page: 106373End Page: 106373Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2023.106373Best OA location URL: https://doi.org/10.1016/j.nbd.2023.106373Citation Count: 13
- Single-cell transcriptomics for immune profiling of cerebrospinal fluid in neurological diseases2025OPENTitle: Single-cell transcriptomics for immune profiling of cerebrospinal fluid in neurological diseasesJournal Name: Frontiers in ImmunologyPublisher: Frontiers Media SAVol: 16Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fimmu.2025.1599303Best OA location URL: https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1599303/pdfCitation Count: 0
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OPENTitle: An unusual presentation of Huntington’s disease-like syndrome in a patient with Xeroderma pigmentosum type F: Case report and review of the literatureJournal Name: Clinical Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 12Issue #:Start Page: 100340End Page: 100340Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.prdoa.2025.100340Best OA location URL: https://doi.org/10.1016/j.prdoa.2025.100340Citation Count: 0
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OPENTitle: a-synuclein PET Imaging: From Clinical Utility in Multiple System Atrophy to the Possible Diagnosis of Parkinson’s DiseaseJournal Name: CellsPublisher: MDPI AGVol: 14Issue #: 11Start Page: 834End Page: 834Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/cells14110834Best OA location URL: https://www.mdpi.com/2073-4409/14/11/834/pdf?version=1748956205Citation Count: 0
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OPENTitle: Machine Learning Interface for Medical Image AnalysisJournal Name: Journal of Digital ImagingPublisher: Springer Science and Business Media LLCVol: 30Issue #: 5Start Page: 615End Page: 621Publication Date:Open Access(OA) Status: OPENLicense: apache-2.0DOI - Digital Object Identifier: 10.1007/s10278-016-9910-0Best OA location URL: https://link.springer.com/content/pdf/10.1007/s10278-016-9910-0.pdfCitation Count: 58
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OPENTitle: Saturation mutagenesis of α-synuclein reveals monomer fold that modulates aggregationJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 9Issue #: 43Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1126/sciadv.adh3457Best OA location URL: https://doi.org/10.1126/sciadv.adh3457Citation Count: 10
- Incident impulse control disorder symptoms and dopamine transporter imaging in Parkinson disease2015OPENTitle: Incident impulse control disorder symptoms and dopamine transporter imaging in Parkinson diseaseJournal Name: Journal of Neurology, Neurosurgery & PsychiatryPublisher: BMJVol: 87Issue #: 8Start Page: 864End Page: 870Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1136/jnnp-2015-311827Best OA location URL: http://doi.org/10.1136/jnnp-2015-311827Citation Count: 121
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OPENTitle: Presence of cerebral amyloid modulates phenotype and pattern of neurodegeneration in early Parkinson's diseaseJournal Name: Journal of Neurology, Neurosurgery & PsychiatryPublisher: BMJVol: 87Issue #: 10Start Page: 1112End Page: 1122Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1136/jnnp-2015-312690Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/5154297Citation Count: 36
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OPENTitle: Clinical-genetic model predicts incident impulse control disorders in Parkinson's diseaseJournal Name: Journal of Neurology, Neurosurgery & PsychiatryPublisher: BMJVol: 87Issue #: 10Start Page: 1106End Page: 1111Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1136/jnnp-2015-312848Best OA location URL: https://hal.sorbonne-universite.fr/hal-01306745Citation Count: 111