Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
<p>The adult neurodegenerative disorder amyotrophic lateral sclerosis (ALS) is unmistakeable from clinical descriptions now more than a century old.1 Neither the site of symptom onset in ALS2 nor pattern of symptom spread3–5 is truly random. While the most consistent signs relate to motor syst...
| Autores principales: | , , , , |
|---|---|
| Formato: | Journal article |
| Publicado: |
BMJ Publishing Group
2018
|