Acta neuropathologica

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia.

C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies.

MSA prions exhibit remarkable stability and resistance to inactivation.

MSA prions exhibit remarkable stability and resistance to inactivation.

Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia.

Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia.

Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.

Towards authentic transgenic mouse models of heritable PrP prion diseases.

Towards authentic transgenic mouse models of heritable PrP prion diseases.

Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.

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