Kamphorst, W.

patient disease mutation dementia brain family frontotemporal dementia study frontotemporal protein inclusion family history antibody ftd þ mnd supranuclear palsy history analysis neurol netherland cortex pathology group sample motor neuron disease neuron frontotemporal lobar degeneration control neurology onset 4 r tau region supranuclear palsy motor isoform expression k 280 mutation disease duration tau gene parkinsonism p 301l mutation staining tau protein substantia nigra degeneration diagnosis pathway chromosome survival result relative -43 ubiquitin-positive alzheimer ftd patients atrophy neuropathol tau mutations p 301l protein tau-p number sclerosis figure ratio nucleus prevalence change table autosomal symptom ubiquitin-positive inclusions duration factor probe netherlands brain bank signi lobar disorder rosso microtubule