Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients

The exploration of accurate diagnostic markers for differential diagnosis of neurodegenerative diseases is an ongoing topic. A previous study on cerebrospinal fluid (CSF)-mitochondrial malate dehydrogenase 1 (MDH1) in sporadic Creutzfeldt–Jakob disease (sCJD) patients revealed a highly significant u...

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Detalles Bibliográficos
Autores principales: Zerr, Inga, Villar-Piqué, Anna, Schmitz, Vanda Edit, Poleggi, Anna, Pocchiari, Maurizio, Sánchez-Valle, Raquel, Calero, Miguel, Calero, Olga, Baldeiras, Inês, Santana, Isabel, Kovacs, Gabor G., Llorens, Franc, Schmitz, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995564/
https://www.ncbi.nlm.nih.gov/pubmed/31795176
http://dx.doi.org/10.3390/biom9120800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995564/
https://www.ncbi.nlm.nih.gov/pubmed/31795176
http://dx.doi.org/10.3390/biom9120800

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