Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease, which is characterized by
the degeneration of motor neurons in the motor cortex and the spinal cord and subsequently …

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that primarily affects the
motor system and presents with progressive muscle weakness. Most patients survive for …

Amyotrophic lateral sclerosis (ALS) is characterized by the progressive loss of somatic motor
neurons. A major focus has been directed to motor neuron intrinsic properties as a cause for …

Striking advances in our understanding of the genetic heterogeneity of ALS continue to be
made, year on year. These implicate proteostasis, RNA export, nuclear transport, the …

Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disease that primarily
affects motor neurons and is accompanied by sustained unregulated immune responses …

Heterogeneity of motor phenotypes is a clinically well-recognized fundamental aspect of
amyotrophic lateral sclerosis (ALS) and is determined by variability of 3 independent primary …

In classic neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), the
pathogenic concept of a cell‐autonomous disease of motor neurons has been challenged …

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease associated with
motor neuron degeneration, muscle atrophy and paralysis. Although numerous pathological …

Amyotrophic lateral sclerosis is a rare and fatal neurodegenerative disease characterised by
progressive deterioration of upper and lower motor neurons that eventually culminates in …

Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease
that leads to the massive loss of motor neurons in cerebrum, brain stem and spinal cord. It …