Genotype–Phenotype Correlation in Progressive Supranuclear Palsy Syndromes: Clinical and Radiological Similarities and Specificities

The progressive supranuclear palsy (PSP) syndrome encompasses different entities. PSP disease of sporadic origin is the most frequent presentation, but different genetic mutations can lead either to monogenic variants of PSP disease, or to other conditions with a different pathophysiology that event...

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Detalles Bibliográficos
Autores principales: Ruiz-Barrio, Iñigo, Horta-Barba, Andrea, Illán-Gala, Ignacio, Kulisevsky, Jaime, Pagonabarraga, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087829/
https://www.ncbi.nlm.nih.gov/pubmed/35557621
http://dx.doi.org/10.3389/fneur.2022.861585

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087829/
https://www.ncbi.nlm.nih.gov/pubmed/35557621
http://dx.doi.org/10.3389/fneur.2022.861585

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