Compounds > pyrrolidonecarboxylic acid

pyrrolidonecarboxylic acid and Deficiency, Mental

pyrrolidonecarboxylic acid has been researched along with Deficiency, Mental in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19904 (66.67)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yamaguchi, S1
Brundelet, PJ; Jellum, E; Marstein, S; Schrader, H; Skullerud, K1
Porath, U; Schreier, K1
Buchanan, DN; Muenzer, J; Robertson, PL1
Antener, I; Mollica, F; Pavone, L1
Eldjarn, L; Jellum, E; Stokke, O1

Reviews

1 review(s) available for pyrrolidonecarboxylic acid and Deficiency, Mental

ArticleYear
[Organic acid disorders: cerebral organic acidemia].
    Ryoikibetsu shokogun shirizu, 2002, Issue:37 Pt 6

    Topics: Brain Diseases, Metabolic; Canavan Disease; Glutarates; Glycerol; Humans; Hydroxybutyrates; Infant; Infant, Newborn; Intellectual Disability; Metabolism, Inborn Errors; Mevalonic Acid; Pyrrolidonecarboxylic Acid; Seizures

2002

Other Studies

5 other study(ies) available for pyrrolidonecarboxylic acid and Deficiency, Mental

ArticleYear
The cerebral lesions in a patient with generalized glutathione deficiency and pyroglutamic aciduria (5-oxoprolinuria).
    Acta neuropathologica, 1980, Volume: 52, Issue:3

    Topics: Adult; Autopsy; Brain; Glutathione; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Pyrrolidonecarboxylic Acid

1980
[A family with pyroglutamic aciduria (author's transl)].
    Deutsche medizinische Wochenschrift (1946), 1978, Jun-02, Volume: 103, Issue:22

    Topics: Acetates; Amino Acid Metabolism, Inborn Errors; Child; Erythrocytes; Female; Genes, Recessive; Glutathione Synthase; Heterozygote; Humans; Infant; Infant, Newborn; Intellectual Disability; Macular Degeneration; Male; Pyrrolidinones; Pyrrolidonecarboxylic Acid; Renal Aminoacidurias

1978
5-Oxoprolinuria in an adolescent with chronic metabolic acidosis, mental retardation, and psychosis.
    The Journal of pediatrics, 1991, Volume: 118, Issue:1

    Topics: Acidosis; Child; Chronic Disease; Female; Glutathione Synthase; Humans; Intellectual Disability; Metabolism, Inborn Errors; Neurocognitive Disorders; Pyrrolidonecarboxylic Acid

1991
Familial hyperprolinemia without mental retardation and hereditary nephropathy.
    Monographs in human genetics, 1972, Volume: 6

    Topics: Amino Acid Metabolism, Inborn Errors; Epilepsy; Female; Glycine; Humans; Infant; Intellectual Disability; Kidney Diseases; Male; Proline; Pyrrolidonecarboxylic Acid

1972
Pyroglutamic aciduria: studies on the enzymic block and on the metabolic origin of pyroglutamic acid.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 40, Issue:2

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Bicarbonates; Biodegradation, Environmental; Carbon Isotopes; Chromatography, Gas; Chromatography, Thin Layer; Diet; Glutamates; Humans; Intellectual Disability; Kidney; Male; Pyrrolidinones; Pyrrolidonecarboxylic Acid; Pyruvates; Quaternary Ammonium Compounds; Time Factors; Urea

1972