Journal of Neurology, Neurosurgery & Psychiatry
Fecha de publicación: 11 April 2019
DOI: http://dx.doi.org/10.1136/jnnp-2017-317245
Autores: Robert D Henderson, Fleur C Garton, Matthew C Kiernan, Martin R Turner, Andrew Eisen.
Background: The adult neurodegenerative disorder amyotrophic lateral sclerosis (ALS) is unmistakeable from clinical descriptions now more than a century old. Neither the site of symptom onset in ALS nor pattern of symptom spread is truly random.
