Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity

Ataxia is increasingly being recognized as a cardinal manifestation in primary mitochondrial diseases (PMDs) in both paediatric and adult patients. It can be caused by disruption of cerebellar nuclei or fibres, its connection with the brainstem, or spinal and peripheral lesions leading to propriocep...

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Detalles Bibliográficos
Autores principales: Lopriore, Piervito, Ricciarini, Valentina, Siciliano, Gabriele, Mancuso, Michelangelo, Montano, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036286/
https://www.ncbi.nlm.nih.gov/pubmed/35466209
http://dx.doi.org/10.3390/neurolint14020028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036286/
https://www.ncbi.nlm.nih.gov/pubmed/35466209
http://dx.doi.org/10.3390/neurolint14020028

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