Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression. Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EM, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G, Yokoyama JS Acta neuropathologica communications
The relationship between complement factor C3, APOE e4, amyloid and tau in Alzheimer's disease. Bonham LW, Desikan RS, Yokoyama JS Acta neuropathologica communications
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. Cali I, Miller CJ, Parisi JE, Geschwind MD, Gambetti P, Schonberger LB 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. 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 Acta neuropathologica communications
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases. Kim MO, Cali I, Oehler A, Fong JC, Wong K, See T, Katz JS, Gambetti P, Bettcher BM, Dearmond SJ, Geschwind MD Acta neuropathologica communications
Topography of FUS pathology distinguishes late-onset BIBD from aFTLD-U. Lee EB, Russ J, Jung H, Elman LB, Chahine LM, Kremens D, Miller BL, Branch Coslett H, Trojanowski JQ, Van Deerlin VM, McCluskey LF Acta neuropathologica communications
