Blood Level of Glial Fibrillary Acidic Protein (GFAP) Does not Correlate With Disease Progression in a Rat Model of Familial ALS (SOD1(G93A) Transgenic)

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by specific loss of motor neurons in the spinal cord and brain stem. Currently, there are limited options for treating ALS and further investigation of the disease etiology and ALS disease progression need to be complet...

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Detalles Bibliográficos
Autores principales: Jeffrey, Jeremy, D'Cunha, Hannah, Suzuki, Masatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246740/
https://www.ncbi.nlm.nih.gov/pubmed/30487774
http://dx.doi.org/10.3389/fneur.2018.00954

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246740/
https://www.ncbi.nlm.nih.gov/pubmed/30487774
http://dx.doi.org/10.3389/fneur.2018.00954

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