Amyotrophic lateral sclerosis (ALS) is an adult onset neurodegenerative disease that results
in motor dysfunction and death, generally from respiratory failure. 90% of ALS cases are …

Spinal cord injury results in a life‐disrupting series of deleterious interconnected
mechanisms encompassed by the primary and secondary injury. These events are mediated …

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease of the motor
nervous system. We show using multielectrode array and patch-clamp recordings that …

Cortical hyperexcitability and mislocalization of the RNA-binding protein TDP43 are highly
conserved features in amyotrophic lateral sclerosis (ALS). Nevertheless, the relationship …

A mechanical trauma to the spinal cord can be followed by the development of irreversible
and progressive neurodegeneration, as opposed to a temporary or partially reversible …

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder in which patients lose
motor functions due to progressive loss of motor neurons in the cortex, brainstem, and spinal …

The convergent endeavors of the neuroscientist to establish a link between clinical
neurology, genetics, loss of function of an important protein, and channelopathies behind …

Objective: To study the relationship between cortical function and survival in amyotrophic
lateral sclerosis (ALS). Methods: A total of 216 referrals were screened, and participants with …

In amyotrophic lateral sclerosis (ALS), abnormalities in motoneuronal excitability are seen in
early pathogenesis and throughout disease progression. Fully understanding motoneuron …

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised by
the loss of motor neurons leading to progressive paralysis and death. Using transcranial …