Cargando…
Neuropathophysiology of Lysosomal Storage Diseases: Synaptic Dysfunction as a Starting Point for Disease Progression
About two thirds of the patients affected with lysosomal storage diseases (LSD) experience neurological manifestations, such as developmental delay, seizures, or psychiatric problems. In order to develop efficient therapies, it is crucial to understand the neuropathophysiology underlying these sympt...
Autores principales: | Pará, Camila, Bose, Poulomee, Pshezhetsky, Alexey V. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141115/ https://www.ncbi.nlm.nih.gov/pubmed/32106459 http://dx.doi.org/10.3390/jcm9030616 |
Ejemplares similares
-
Synaptic Function and Dysfunction in Lysosomal Storage Diseases
por: Rebiai, Rima, et al.
Publicado: (2021) -
Frequency-dependent exacerbation of Alzheimer’s disease neuropathophysiology
por: Kastanenka, Ksenia V., et al.
Publicado: (2019) -
Early defects in mucopolysaccharidosis type IIIC disrupt excitatory synaptic transmission
por: Pará, Camila, et al.
Publicado: (2021) -
Overview of the Role of Vanillin in Neurodegenerative Diseases and Neuropathophysiological Conditions
por: Iannuzzi, Clara, et al.
Publicado: (2023) -
Crosstalk between 2 organelles: Lysosomal storage of heparan sulfate causes mitochondrial defects and neuronal death in mucopolysaccharidosis III type C
por: Pshezhetsky, Alexey V
Publicado: (2015)