Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations.

An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.

Review Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.

Review Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.

Review The involvement of endoplasmic reticulum formation and protein synthesis efficiency in VCP- and ATL1-related neurological disorders.

Review Is amyotrophic lateral sclerosis/frontotemporal dementia an autophagy disease?

Loss of TMEM106B Ameliorates Lysosomal and Frontotemporal Dementia-Related Phenotypes in Progranulin-Deficient Mice.