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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Acta Neuropathologica|July 16, 2008
Evaluation of alpha-synuclein immunohistochemical methods used by invited expertsThomas G Beach, Charles L White, Ronald L Hamilton, et al.
Brain, Behavior, and Immunity|July 10, 2024
A rapidly progressive multiple system atrophy-cerebellar variant model presenting marked glial reactions with inflammation and spreading of α-synuclein oligomers and phosphorylated α-synuclein aggregatesHiroo Yamaguchi, Yuji Nishimura, Dai Matsuse, et al.
Archives of Neurology|February 10, 2010
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Human Genetics|December 7, 2010
Investigation of 15 of the top candidate genes for late-onset Alzheimer's diseaseOlivia Belbin, Minerva M Carrasquillo, Michael Crump, et al.
Archives of Neurology|June 18, 2010
Replication of CLU, CR1, and PICALM associations with alzheimer diseaseMinerva M Carrasquillo, Olivia Belbin, Talisha A Hunter, et al.
Neurology|May 12, 2004
Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ K Wszolek, R F Pfeiffer, Y Tsuboi, et al.
Neurology|June 15, 2018
Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body diseaseKoji Kasanuki, Keith A Josephs, Tanis J Ferman, et al.
JAMA Neurology|October 29, 2019
Selective Vulnerability of the Nucleus Basalis of Meynert Among Neuropathologic Subtypes of Alzheimer DiseaseFadi S Hanna Al-Shaikh, Ranjan Duara, Julia E Crook, et al.
Molecular Neurodegeneration|November 28, 2020
Astrocyte-derived clusterin suppresses amyloid formation in vivoAleksandra M Wojtas, Jonathon P Sens, Silvia S Kang, et al.
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