Arq. NeuroPsiquiatr. vol.75 número5

Key words: dementia, frontotemporal dementia, amyotrophic lateral sclerosis, neuropathology, motor neuron disease.. DEMÊNCIA FRONTOTEMPORAL E ESCLEROSE LATERAL AMIOTRÓFICA:

trophic Lateral Sclerosis of bulbar onset, the domains feeding and communication were the most impaired, while the difficulties in the physical mobility affected the quality of

Depression and anxiety in individuals with amyotrophic lateral sclerosis: a systematic review.. Depressão e ansiedade em pessoas com esclerose

Prefrontal cortex sub-regions of the medial orbitofrontal cortex (MOFC), lateral orbitofrontal cortex (LOFC) and anterior cingulate cortex (ACC), striatal sub-regions of the

Is magnetic resonance imaging a plausible biomarker for upper motor neuron degeneration in amyotrophic lateral sclerosis/primary lateral sclerosis or merely a useful paraclinical

A distinct MR imaging phenotype in amyotrophic lateral sclerosis: correlation between T1 magnetization transfer contrast hyperintensity along the corticospinal tract and

Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies. Microvacuolization of

We describe 03 patients with motor neuron disease: one with primary lateral sclerosis (PLS) (Figure 1) and two with amy- otrophic lateral sclerosis (ALS) (Figures 2 and 3) whose brain