Page last updated: 2024-08-22

n-methylaspartate and Central Nervous System Demyelinating Diseases, Hereditary

n-methylaspartate has been researched along with Central Nervous System Demyelinating Diseases, Hereditary in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cross, AH; Goldberg, MP; Gonzales, E; Pitt, D1

Other Studies

1 other study(ies) available for n-methylaspartate and Central Nervous System Demyelinating Diseases, Hereditary

ArticleYear
Dysmyelinated axons in shiverer mice are highly vulnerable to alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) receptor-mediated toxicity.
    Brain research, 2010, Jan-14, Volume: 1309

    Topics: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Animals; Biomarkers; Brain; Disease Models, Animal; Excitatory Amino Acid Agonists; Female; Hereditary Central Nervous System Demyelinating Diseases; Luminescent Proteins; Mice; Mice, Inbred C57BL; Mice, Neurologic Mutants; Movement Disorders; Myelin Basic Protein; N-Methylaspartate; Nerve Degeneration; Nerve Fibers, Myelinated; Neurotoxins; Receptors, AMPA

2010