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  • Patients with a progressive lower motor neuron disorder with no upper motor neuron signs were classified as having sporadic progressive muscular atrophy (SPMA); those with a progressive upper motor neuron disorder without lower motor neuron signs were classified as having sporadic primary lateral sclerosis (SPLS); and those who had a progressive upper and lower motor neuron disorder involving only the bulbar muscles were classified as having sporadic progressive bulbar palsy (SPBP).
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