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Items: 5

1.
Clinical, neuropathological, and molecular characteristics of rapidly progressive dementia with Lewy bodies: a distinct clinicopathological entity?
Giuseppe Mario Bentivenga, Simone Baiardi, Andrea Mastrangelo, Edoardo Ruggeri, Angela Mammana, Alice Ticca, Marcello Rossi, Sabina Capellari, Piero Parchi
Alzheimers Res Ther. 2024; 16: 201. Published online 2024 Sep 10. doi: 10.1186/s13195-024-01565-x
PMCID:
PMC11384710
AbstractArticlePDF–1.4M
2.
A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom
Tomoyuki Nagata, Shunichiro Shinagawa, Nobuyuki Kobayashi, Kazuhiro Kondo, Masahiro Shigeta
Prion. 2022; 16(1): 7–13. Published online 2021 Dec 29. doi: 10.1080/19336896.2021.2017701
PMCID:
PMC9757407
AbstractArticlePDF–1.1M
3.
Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature
Leonel T. Takada, Mee-Ohk Kim, Ross W. Cleveland, Katherine Wong, Sven A. Forner, Ignacio Illán Gala, Jamie C. Fong, Michael D. Geschwind
Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2020 May 8.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2017 Jan; 174(1): 36–69. doi: 10.1002/ajmg.b.32505
PMCID:
PMC7207989
AbstractArticlePDF–1.1M
4.
Genetic PrP Prion Diseases
Mee-Ohk Kim, Leonel T. Takada, Katherine Wong, Sven A. Forner, Michael D. Geschwind
Cold Spring Harb Perspect Biol. 2018 May; 10(5): a033134. doi: 10.1101/cshperspect.a033134
PMCID:
PMC5932589
AbstractArticlePDF–2.7M
5.
Genome-wide association study of behavioural and psychiatric features in human prion disease
A G B Thompson, J Uphill, J Lowe, M-C Porter, A Lukic, C Carswell, P Rudge, A MacKay, J Collinge, S Mead
Transl Psychiatry. 2015 Apr; 5(4): e552. Published online 2015 Apr 21. doi: 10.1038/tp.2015.42
PMCID:
PMC4462605
AbstractArticlePDF–294K

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