David Mann

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature

Negative regulation of transforming growth factor-β by the proteoglycan decorin

COVID-19 transforms health care through telemedicine: Evidence from the field

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

A harmonized classification system for FTLD-TDP pathology

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update