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Amyotrophic Lateral Sclerosis

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Abstract

Amyotrophic lateral sclerosis (ALS) is a degenerative disorder characterized by loss of motor neurons in the spinal cord, brainstem, and cerebral cortex. It is an uncommon disease with an incidence in the range of 1–2.5 cases per 100,000 population. Incidence increases with age and there is a slight male preponderance. The etiology is unknown, and the progression of the disease is almost uniformly relentless, resulting in death.

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© 2006 Humana Press Inc., Totowa, NJ

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Benatar, M. (2006). Amyotrophic Lateral Sclerosis. In: Benatar, M. (eds) Neuromuscular Disease. Humana Press. https://doi.org/10.1007/978-1-59745-106-2_5

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  • DOI: https://doi.org/10.1007/978-1-59745-106-2_5

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-627-6

  • Online ISBN: 978-1-59745-106-2

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