Vitamin B12 deficiency mimicking neuroimaging features of motor neuron disease

Para a mulher enfermeira, o estresse sofrido no ambiente familiar, social e pessoal, os de fatores de trabalho característicos da profissão, expõe a mulher a

bvFTD: behavioral variant frontotemporal dementia; PNFA: Progressive non-fluent aphasia; GRN: progranulin gene; MND: motor neuron disease; SD: semantic dementia; IBMPFD: inclusion

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

Juvenile onset bul- bospinal muscular atrophy with deafness: Vialetto-van Laere syndrome or Madras type motor neuron disease?. J

We present an unusual report of a patient with EF and clinical and EMG characteristics of a lower neuron disease suggestive of motor neuron disease (MND), such as ALS.. We

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

The spectrum of neurological conditions associated with hexanucleotide repeat expansion of C9orf72 gene is very broad, ranging from the classic phenotype of motor neuron disease

The X-linked spinal and bulbar muscular atrophy (Kennedy’s disease) is a rare X-linked, recessive, lower motor neuron disease, characterized by weakness, atrophy, and fasciculations