Corticobasal Degeneration
What's New
Last Posted: Apr 25, 2024
- MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study.
Rebecca R Valentino, et al. The Lancet. Neurology 2024 0 (5) 487-499 - Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.
Rebecca R Valentino, et al. medRxiv : the preprint server for health sciences 2023 0 - Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series.
Kim Eun-Joo, et al. Journal of neurology 2018 0 (12) 2960-2971 - A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies.
Karch Celeste M, et al. Stem cell reports 2019 0 (5) 939-955 - MAPT p.V363I mutation: A rare cause of corticobasal degeneration.
Ahmed Sarah, et al. Neurology. Genetics 2019 0 (4) e347 - Coexisting Lewy body disease and clinical parkinsonism in frontotemporal lobar degeneration.
Forrest Shelley L, et al. Neurology 2019 0 (21) e2472-e2482 - MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features.
Valentino Rebecca R, et al. Acta neuropathologica communications 2020 0 (1) 218 - Novel tau filament fold in corticobasal degeneration.
Zhang Wenjuan, et al. Nature 2020 0 (7802) 283-287 - Traumatic Brain Injury Exposure Lowers Age of Cognitive Decline in AD and Non-AD Conditions.
Iacono Diego, et al. Frontiers in neurology 2021 0 573401 - Genetic pleiotropy and the shared pathological features of corticobasal degeneration and progressive supranuclear palsy: a case report and a review of the literature.
Rini James, et al. Neurocase 2021 0 (2) 120-128
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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