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phosphorylethanolamine and Amino Acid Metabolism Disorders, Inborn

phosphorylethanolamine has been researched along with Amino Acid Metabolism Disorders, Inborn in 2 studies

phosphorylethanolamine: RN given refers to parent cpd; structure
O-phosphoethanolamine : The ethanolamine mono-ester of phosphoric acid, and a metabolite of phospholipid metabolism. This phosphomonoester shows strong structural similarity to the inhibitory neurotransmitter GABA, and is decreased in post-mortem Alzheimer's disease brain.

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
Kish, SJ1
Robitaille, Y1
el-Awar, M1
Gilbert, J1
Deck, J1
Chang, LJ1
Schut, L1
Zeman, L1
Zeman, J1
Kozich, V1
Matousová, M1
Velísková, J1

Other Studies

2 other studies available for phosphorylethanolamine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy.
    Annals of neurology, 1991, Volume: 30, Issue:6

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartic Acid; Brain Chemistry; Chromosome

1991
[Phosphoethanolamine in the blood and urine in sick children].
    Ceskoslovenska pediatrie, 1991, Volume: 46, Issue:1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Ethanolamines; Hum

1991