The morbid anatomy of dementia in Parkinson's disease
Monoclonal antibody specific for IDH1 R132H mutation
GFAP, Ki67 and IDH1
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
FUS pathology in basophilic inclusion body disease
Frontotemporal lobar degeneration
TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy
Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types
The anterior cingulate cortex in autism
Llama VHH antibody fragments against GFAP
Leigh-like subacute necrotising encephalopathy in Yorkshire Terriers
Vacuolar myopathy in a dog resembling human sporadic inclusion body myositis
Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene
Kurt Jellinger Prize 2010 for Outstanding Scientific Writing in Neuropathology