Amyotrophic lateral sclerosis (ALS) is a neuromuscular condition resulting from the
progressive degeneration of motor neurons in the cortex, brainstem, and spinal cord. While …

Amyotrophic lateral sclerosis (ALS), the most common adult onset motor neuron disease, is
pathologically characterized by progressive loss of the upper and lower motor neurons …

Amyotrophic Lateral Sclerosis (ALS) is a progressive motor neurodegenerative disease. Cell
damage in ALS is the result of many different, largely unknown, pathogenetic mechanisms …

Amyotrophic lateral sclerosis (ALS) is characterized by adult-onset progressive
degeneration of upper and lower motor neurons. Increasing numbers of genes are found to …

Amyotrophic lateral sclerosis (ALS) is a fatal heterogeneous neurodegenerative disease that
causes motor neuron (MN) loss and skeletal muscle paralysis. It is uncertain whether this …

Amyotrophic lateral sclerosis (ALS) is a progressive and fatal disorder characterized by
degeneration of motor neurons in the cerebral cortex, brain stem, and spinal cord. Most …

Mutations in superoxide dismutase 1 (SOD1) result in misfolding and aggregation of the
protein, causing neurodegenerative amyotrophic lateral sclerosis (ALS). In recent years …

Amyotrophic lateral sclerosis (ALS) is a devastating neurologic disease that rapidly
progresses from mild motor symptoms to severe motor paralysis and premature death. Until …

Amyotrophic lateral sclerosis (ALS) is a devastating paralytic disorder caused by motor
neuron degeneration. A subgroup of familial cases arises from mutations in the gene …

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by
the loss of motor neurons in the brain and spinal cord. While the exact causes of ALS are still …