Page last updated: 2024-10-31

minaprine and Amyotrophic Lateral Sclerosis

minaprine has been researched along with Amyotrophic Lateral Sclerosis in 1 studies

minaprine: Agr 1240 refers to di-HCl; short-acting type A MAO inhibitor (MAOI) of mild potency; structure

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 (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
Chen, T1
Benmohamed, R1
Kim, J1
Smith, K1
Amante, D1
Morimoto, RI1
Kirsch, DR1
Ferrante, RJ1
Silverman, RB1

Other Studies

1 other study available for minaprine and Amyotrophic Lateral Sclerosis

ArticleYear
ADME-guided design and synthesis of aryloxanyl pyrazolone derivatives to block mutant superoxide dismutase 1 (SOD1) cytotoxicity and protein aggregation: potential application for the treatment of amyotrophic lateral sclerosis.
    Journal of medicinal chemistry, 2012, Jan-12, Volume: 55, Issue:1

    Topics: Amyotrophic Lateral Sclerosis; Animals; Blood-Brain Barrier; Caco-2 Cells; Cell Membrane Permeabilit

2012