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linsidomine and Amyotrophic Lateral Sclerosis

linsidomine has been researched along with Amyotrophic Lateral Sclerosis in 3 studies

linsidomine: RN given refers to parent cpd; 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 Excerpts

ExcerptRelevanceReference
"Reactive astrogliosis and dysfunctional transporters for L-glutamate [excitatory amino acid transporters, (EAATs)] are hallmarks of ALS pathology."1.35Oxidative and excitotoxic insults exert differential effects on spinal motoneurons and astrocytic glutamate transporters: Implications for the role of astrogliosis in amyotrophic lateral sclerosis. ( Beart, PM; Nagley, P; O'Shea, RD; Wallis, N; Zagami, CJ, 2009)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Zagami, CJ1
Beart, PM1
Wallis, N1
Nagley, P1
O'Shea, RD1
Kupershmidt, L1
Weinreb, O1
Amit, T1
Mandel, S1
Carri, MT1
Youdim, MB1
Aguirre, T1
Van Den Bosch, L1
Goetschalckx, K1
Tilkin, P1
Mathijs, G1
Cassiman, JJ1
Robberecht, W1

Other Studies

3 other studies available for linsidomine and Amyotrophic Lateral Sclerosis

ArticleYear
Oxidative and excitotoxic insults exert differential effects on spinal motoneurons and astrocytic glutamate transporters: Implications for the role of astrogliosis in amyotrophic lateral sclerosis.
    Glia, 2009, Jan-15, Volume: 57, Issue:2

    Topics: Amyotrophic Lateral Sclerosis; Animals; Anterior Horn Cells; Astrocytes; Cell Survival; Cells, Cultu

2009
Neuroprotective and neuritogenic activities of novel multimodal iron-chelating drugs in motor-neuron-like NSC-34 cells and transgenic mouse model of amyotrophic lateral sclerosis.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2009, Volume: 23, Issue:11

    Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Brain-Derived Neurotrophic Factor; Cell Different

2009
Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stress.
    Annals of neurology, 1998, Volume: 43, Issue:4

    Topics: Amyotrophic Lateral Sclerosis; Cell Survival; Cells, Cultured; Enzyme Inhibitors; Fibroblasts; Human

1998