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gyki 52466 and Amyotrophic Lateral Sclerosis

gyki 52466 has been researched along with Amyotrophic Lateral Sclerosis in 2 studies

GYKI 52466: an AMPA (non-NMDA) receptor antagonist; structure given in first source

Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rothstein, JD1
Bristol, LA1
Hosler, B1
Brown, RH1
Kuncl, RW1
Vartiainen, N1
Tikka, T1
Keinänen, R1
Chan, PH1
Koistinaho, J1

Other Studies

2 other studies available for gyki 52466 and Amyotrophic Lateral Sclerosis

ArticleYear
Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons.
    Proceedings of the National Academy of Sciences of the United States of America, 1994, May-10, Volume: 91, Issue:10

    Topics: Acetylcysteine; Amyotrophic Lateral Sclerosis; Animals; Animals, Newborn; Anti-Anxiety Agents; Antio

1994
Glutamatergic receptors regulate expression, phosphorylation and accumulation of neurofilaments in spinal cord neurons.
    Neuroscience, 1999, Volume: 93, Issue:3

    Topics: 6-Cyano-7-nitroquinoxaline-2,3-dione; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Amyo

1999