Cargando…
Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia
BACKGROUND: SPG11-linked hereditary spastic paraplegia is characterized by multisystem neurodegeneration leading to a complex clinical and yet incurable phenotype of progressive spasticity and weakness. Severe cognitive symptoms are present in the majority of SPG11 patients, but a systematic and mul...
Autores principales: | Utz, Kathrin S., Kohl, Zacharias, Marterstock, Dominique Cornelius, Doerfler, Arnd, Winkler, Jürgen, Schmidt, Manuel, Regensburger, Martin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336101/ https://www.ncbi.nlm.nih.gov/pubmed/35906604 http://dx.doi.org/10.1186/s13023-022-02451-1 |
Ejemplares similares
-
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
por: Regensburger, Martin, et al.
Publicado: (2022) -
Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
por: Pérez-Brangulí, Francesc, et al.
Publicado: (2014) -
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11
por: Renvoisé, Benoît, et al.
Publicado: (2014) -
Clinical analysis in patients with SPG11 hereditary spastic paraplegia
por: Kang, You-Ri, et al.
Publicado: (2023) -
Ascending Axonal Degeneration of the Corticospinal Tract in Pure Hereditary Spastic Paraplegia: A Cross-Sectional DTI Study
por: List, Julia, et al.
Publicado: (2019)