Acta neuropathologica communications

Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants.

Acta neuropathologica communications

Lin LC, Nana AL, Hepker M, Hwang JL, Gaus SE, Spina S, Cosme CG, Gan L, Grinberg LT, Geschwind DH, Coppola G, Rosen HJ, Miller BL, Seeley WW

Early neuronal accumulation of DNA double strand breaks in Alzheimer's disease.

Acta neuropathologica communications

Shanbhag NM, Evans MD, Mao W, Nana AL, Seeley WW, Adame A, Rissman RA, Masliah E, Mucke L

Characterization of tau prion seeding activity and strains from formaldehyde-fixed tissue.

Acta neuropathologica communications

Kaufman SK, Thomas TL, Del Tredici K, Braak H, Diamond MI

Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.

Acta neuropathologica communications

Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EM, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G, Yokoyama JS

Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.

Acta neuropathologica communications

Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EM, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G, Yokoyama JS

The relationship between complement factor C3, APOE e4, amyloid and tau in Alzheimer's disease.

Acta neuropathologica communications

Bonham LW, Desikan RS, Yokoyama JS

The relationship between complement factor C3, APOE e4, amyloid and tau in Alzheimer's disease.

Acta neuropathologica communications

Bonham LW, Desikan RS, Yokoyama JS

Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.

Acta neuropathologica communications

Cali I, Miller CJ, Parisi JE, Geschwind MD, Gambetti P, Schonberger LB

Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.

Acta neuropathologica communications

Cali I, Miller CJ, Parisi JE, Geschwind MD, Gambetti P, Schonberger LB

A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques.

Acta neuropathologica communications

Moreno F, Rabinovici GD, Karydas A, Miller Z, Hsu SC, Legati A, Fong J, Schonhaut D, Esselmann H, Watson C, Stephens ML, Kramer J, Wiltfang J, Seeley WW, Miller BL, Coppola G, Grinberg LT

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