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- W952474137 abstract "This chapter discusses the atrophies of the motor neurons. Diseases belonging to this group are: amyotrophic lateral sclerosis (ALS), bulbar palsy, spinal spastic paralysis, progressive external ophthalmoplegia, and the spinal muscular atrophies. ALS is described as the disease of the upper and lower motor neurons. It comprises sporadic, endemic, and familial forms. The majority of the patients with ALS belong to the sporadic group. Spinal spastic paralysis may appear in a pure or complicated form and affects several members of a family. The lower limbs are predominantly affected. In the dominant form, two types are distinguished: type I and type II. Several cases of an association of motor neuron disease with dementia have been reported. Dementia usually precedes the onset of motor symptoms, sometimes by as much as 2 years, but occasionally follows it." @default.
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- W952474137 date "1995-01-01" @default.
- W952474137 modified "2023-10-11" @default.
- W952474137 title "Atrophies of the Motor Neurons" @default.
- W952474137 doi "https://doi.org/10.1016/b978-012165250-0/50018-0" @default.
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