Acta neuropathologica communications

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

Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases.

Acta neuropathologica communications

Kim MO, Cali I, Oehler A, Fong JC, Wong K, See T, Katz JS, Gambetti P, Bettcher BM, Dearmond SJ, Geschwind MD

Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases.

Acta neuropathologica communications

Kim MO, Cali I, Oehler A, Fong JC, Wong K, See T, Katz JS, Gambetti P, Bettcher BM, Dearmond SJ, Geschwind MD

Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U.

Acta neuropathologica communications

Lee EB, Russ J, Jung H, Elman LB, Chahine LM, Kremens D, Miller BL, Branch Coslett H, Trojanowski JQ, Van Deerlin VM, McCluskey LF

Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U.

Acta neuropathologica communications

Lee EB, Russ J, Jung H, Elman LB, Chahine LM, Kremens D, Miller BL, Branch Coslett H, Trojanowski JQ, Van Deerlin VM, McCluskey LF

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