Projects per year
Although amyotrophic lateral sclerosis (ALS) is pre-eminently a motor disease, the existence of non-motor manifestations, including sensory involvement, has been described in the last few years. Although from a clinical perspective, sensory symptoms are overshadowed by their motor manifestations, this does not mean that their pathological significance is not relevant. In this review, we have made an extensive description of the involvement of sensory and autonomic systems described to date in ALS, from clinical, neurophysiological, neuroimaging, neuropathological, functional, and molecular perspectives
|Number of pages||32|
|Journal||International journal of molecular sciences|
|Publication status||Published - 8 Dec 2022|
- ALS; small fiber; sensory; autonomic; proprioceptive; somatosensory
FingerprintDive into the research topics of 'Sensory Involvement in Amyotrophic Lateral Sclerosis'. Together they form a unique fingerprint.
- 1 Finished
PAPEL DEL RECEPTOR SIGMA1 EN LA MODULACION DE LAS DISFUNCIONES DE LA MEMBRANA DEL RETICULO ENDOPLASMATICO ASOCIADA A MITOCONDRIA (MAM) EN LA DEGENERACION DE MOTONEURONAS
Navarro Acebes, X. & Herrando Grabulosa, M.
1/01/19 → 30/09/22
Project: Research Projects and Other Grants