Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?
Amyotrophic lateral sclerosis (ALS) is typically regarded as a sporadic neurodegenerative disorder that results in a catastrophic failure of the motor system, with characteristically variable involvement of upper and lower motor neuronal populations. A wide range of evidence from clinical, histologi...
Κύριοι συγγραφείς: | Turner, M, Kiernan, M |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2012
|
Παρόμοια τεκμήρια
-
The Neonatal Microbiome: Implications for Amyotrophic Lateral Sclerosis and Other Neurodegenerations
ανά: Andrew Eisen, κ.ά.
Έκδοση: (2025-02-01) -
Potential contribution of spinal interneurons to the etiopathogenesis of amyotrophic lateral sclerosis
ανά: Luca Goffin, κ.ά.
Έκδοση: (2024-07-01) -
Biomarkers in amyotrophic lateral sclerosis.
ανά: Turner, M, κ.ά.
Έκδοση: (2009) -
Amyotrophic lateral sclerosis.
ανά: Kiernan, M, κ.ά.
Έκδοση: (2011) -
Regional motor cortex dysfunction in amyotrophic lateral sclerosis
ανά: Parvathi Menon, κ.ά.
Έκδοση: (2019-08-01)