Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series

OBJECTIVE: To perform a comprehensive clinical characterization and biochemical CSF profile analyses in 2 Swedish families with hereditary spastic paraparesis (HSP) 10 (SPG10) caused by 2 different mutations in the neuronal kinesin heavy chain gene (KIF5A). METHODS: Structured clinical assessment, g...

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Detalles Bibliográficos
Autores principales: Andréasson, Mattias, Lagerstedt-Robinson, Kristina, Samuelsson, Kristin, Solders, Göran, Blennow, Kaj, Paucar, Martin, Svenningsson, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659133/
https://www.ncbi.nlm.nih.gov/pubmed/31403080
http://dx.doi.org/10.1212/NXG.0000000000000344

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659133/
https://www.ncbi.nlm.nih.gov/pubmed/31403080
http://dx.doi.org/10.1212/NXG.0000000000000344

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