lateral sclerosis


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lateral sclerosis

[′lad·ə·rəl sklə′rō·səs]
References in periodicals archive ?
NPT520-34 also has been shown to reduce the expression of markers of neuroinflammation and neuropathology in animal models of amyotrophic lateral sclerosis and Alzheimer's disease.
ROF is a novel formulation of riluzole that is used as an adjunctive therapy in the treatment of amyotrophic lateral sclerosis (ALS).
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disease, characterized by the involvement of both upper motor neurons (UMNs) and lower motor neurons (LMNs).
'We hope that the clinical test will be successful to suppress progression of symptoms so that body functions remain, even if only a little,' said Shigeyuki Shimamori, chairman of the Japan Amyotrophic Lateral Sclerosis Association.
Amyotrophic lateral sclerosis (ALS) is reportedly a rare, rapidly progressive, and always fatal neurodegenerative disease.
Niven, who suffered for more than a year from amyotrophic lateral sclerosis, a debilitating neuromuscular disorder, died, said Jane Sylvester of Cowan Bellew publicity agents.
The study, "The vulnerability of spinal motoneurons and soma size plasticity in a mouse model of amyotrophic lateral sclerosis," was published in The Journal of Physiology.
He was, simultaneously, a source of inspiration for both scientists and patients of amyotrophic lateral sclerosis (ALS).
Amyotrophic lateral sclerosis (ALS) is one of the neurodegenerative diseases that is characterized by a progressive loss of the upper and lower motor neurons at the motor cortex, spinal, and bulbar levels.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive and selective death of upper and lower motor neurons, in the cerebral cortex and spinal cord.