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Key terms:
als
motor neuron
atrophy
glutamate
ventilation
familial
als patients
riluzole
hospice
help patients
patients experience
therapists
spasticity
spinal cord
tracheostomy
familial als
motor neuron degeneration
amyotrophic lateral sclerosis
als association
diagnosis of als
lower motor neuron
ventilation support
patients and caregivers
muscle weakness and atrophy
bipap
spinal fluid
treatment for als
impair
multiple sclerosis
mouse model
sporadic als
energy intake
choking
superoxide dismutase
progression of als
motor neuron disease
risk factor
lou gehrig
rnai
patients with als
nourishment
bulbar onset
neurological disorders
mechanical ventilation
frontotemporal
onset als
positive pressure ventilation
upper motor neuron
hrbek
free radicals
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