The past year has seen a number of significant advances in our understanding of the
neuropathological and molecular genetic basis of frontotemporal lobar degeneration …

The clinical disorders associated with frontotemporal lobar degeneration (FTLD) are
increasingly recognized as an important cause of early-onset dementia. Patients usually …

The aim of this study was to improve the neuropathologic recognition and provide criteria for
the pathological diagnosis in the neurodegenerative diseases grouped as frontotemporal …

Frontotemporal lobar degeneration (FTLD) represents a collection of neurodegenerative
diseases of frontal and temporal brain regions. It has long been associated with mutations in …

Frontotemporal lobar degeneration (FTLD), the most frequent neurodegenerative disorder
with a presenile onset, presents with a spectrum of clinical manifestations, ranging from …

Great strides have been made in the last 2 years in the field of frontotemporal lobar
degeneration (FTLD), particularly with respect to the genetics and molecular biology of FTLD …

Frontotemporal lobar degeneration (FTLD) refers to a focal, non-Alzheimer form of cerebral
degeneration that encompasses the distinct clinical syndromes of frontotemporal dementia …

Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders
characterized by disturbances of behavior and personality and different types of language …

Frontotemporal lobar degeneration (FTLD) is now a widely recognised form of dementia.
This heterogeneous disease has been of particular interest to geneticists due to its high rate …

Frontotemporal lobar degeneration (FTLD) is a clinically, pathologically and genetically
highly complex disorder. In the last few years enormous progress has been made in …