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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

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