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Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases.
Zhang W, Orrú CD, Foutz A, Ding M, Yuan J, Shah SZA, Zhang J, Kotobelli K, Gerasimenko M, Gilliland T, Chen W, Tang M, Cohen M, Safar J, Xu B, Hong DJ, Cui L, Hughson AG, Schonberger LB, Tatsuoka C, Chen SG, Greenlee JJ, Wang Z, Appleby BS, Caughey B, Zou WQ. Zhang W, et al. Among authors: appleby bs. Acta Neuropathol. 2024 Jan 17;147(1):17. doi: 10.1007/s00401-023-02661-2. Acta Neuropathol. 2024. PMID: 38231266
Correction: A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
Bayazid R, Orru' C, Aslam R, Cohen Y, Silva-Rohwer A, Lee SK, Occhipinti R, Kong Q, Shetty S, Cohen ML, Caughey B, Schonberger LB, Appleby BS, Cali I. Bayazid R, et al. Among authors: appleby bs. Acta Neuropathol. 2023 Jul;146(1):167-170. doi: 10.1007/s00401-023-02592-y. Acta Neuropathol. 2023. PMID: 37253983 Free PMC article. No abstract available.
Genetic aspects of human prion diseases.
Appleby BS, Shetty S, Elkasaby M. Appleby BS, et al. Front Neurol. 2022 Oct 5;13:1003056. doi: 10.3389/fneur.2022.1003056. eCollection 2022. Front Neurol. 2022. PMID: 36277922 Free PMC article. Review.
Creutzfeldt-Jakob Disease Misdiagnosed as Multiple System Atrophy.
Martin NB, Koga S, Appleby BS, Sekiya H, Dickson D. Martin NB, et al. Among authors: appleby bs. Mov Disord Clin Pract. 2023 Jan 20;10(3):496-500. doi: 10.1002/mdc3.13654. eCollection 2023 Mar. Mov Disord Clin Pract. 2023. PMID: 36949796 Free PMC article.
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.
Stephen CD, de Gusmao CM, Srinivasan SR, Olsen A, Freua F, Kok F, Montes Garcia Barbosa R, Chen JYH, Appleby BS, Prior T, Frosch MP, Schmahmann JD. Stephen CD, et al. Among authors: appleby bs. Mov Disord Clin Pract. 2024 Apr;11(4):411-423. doi: 10.1002/mdc3.13976. Epub 2024 Jan 23. Mov Disord Clin Pract. 2024. PMID: 38258626
97 results