Cargando…
Neurological Phenotypes in Mouse Models of Mitochondrial Disease and Relevance to Human Neuropathology
Mitochondrial diseases represent the most common inherited neurometabolic disorders, for which no effective therapy currently exists for most patients. The unmet clinical need requires a more comprehensive understanding of the disease mechanisms and the development of reliable and robust in vivo mod...
Autores principales: | Olkhova, Elizaveta A., Smith, Laura A., Bradshaw, Carla, Gorman, Gráinne S., Erskine, Daniel, Ng, Yi Shiau |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254022/ https://www.ncbi.nlm.nih.gov/pubmed/37298649 http://dx.doi.org/10.3390/ijms24119698 |
Ejemplares similares
-
A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction
por: Olkhova, Elizaveta A., et al.
Publicado: (2023) -
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors
por: Pickett, Sarah J., et al.
Publicado: (2018) -
l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes: A Systematic Review
por: Stefanetti, Renae J., et al.
Publicado: (2022) -
Arrhythmia prevalence and sudden death risk in adults with the m.3243A>G mitochondrial disorder
por: Bourke, John P, et al.
Publicado: (2022) -
Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study
por: Braz, Luis P., et al.
Publicado: (2021)