Compounds > n-acetylaspartic acid
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n-acetylaspartic acid and Inborn Errors of Metabolism

n-acetylaspartic acid has been researched along with Inborn Errors of Metabolism in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's2 (40.00)18.2507
2000's2 (40.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Berry, GT; Jan, W; Kaplan, PB; Kaye, EM; Wang, ZJ; Zimmerman, RA1
Amorini, AM; Bellia, F; Ceccarelli, L; Di Pietro, V; Donzelli, S; Francis, JS; Giardina, B; Janson, CG; Lazzarino, G; Leone, P; Tavazzi, B1
Bruhn, H; Frahm, J; Hanefeld, F; Kruse, B1
Ernst, S; Heindel, W; Kugel, H; Lackner, K; Roth, B1
Divry, P; Mathieu, M1

Other Studies

5 other study(ies) available for n-acetylaspartic acid and Inborn Errors of Metabolism

ArticleYear
MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.
    Neuroradiology, 2003, Volume: 45, Issue:6

    Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Amino Acids, Branched-Chain; Aspartic Acid; Basal Ganglia; Biomarkers; Brain Stem; Cerebellum; Cerebral Cortex; Creatine; Diffusion Magnetic Resonance Imaging; Female; Follow-Up Studies; Humans; Infant; Infant Welfare; Infant, Newborn; Ketone Oxidoreductases; Lactic Acid; Magnetic Resonance Spectroscopy; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Multienzyme Complexes; Phosphocreatine; Radiography; Statistics as Topic; Time Factors

2003
Simultaneous high performance liquid chromatographic separation of purines, pyrimidines, N-acetylated amino acids, and dicarboxylic acids for the chemical diagnosis of inborn errors of metabolism.
    Clinical biochemistry, 2005, Volume: 38, Issue:11

    Topics: Adolescent; Adult; Amino Acids; Amniotic Fluid; Aspartic Acid; Canavan Disease; Child; Child, Preschool; Chromatography, High Pressure Liquid; Dicarboxylic Acids; Humans; Infant; Mass Screening; Metabolism, Inborn Errors; Middle Aged; Prenatal Diagnosis; Purines; Pyrimidines; Reproducibility of Results; Sensitivity and Specificity; Spectrophotometry, Ultraviolet

2005
In vivo proton magnetic resonance spectroscopy of the brain in a patient with L-2-hydroxyglutaric acidemia.
    Pediatric research, 1994, Volume: 35, Issue:5

    Topics: Adolescent; Aspartic Acid; Biomarkers; Brain; Female; Glutarates; Humans; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Metabolism, Inborn Errors; Nerve Degeneration

1994
Proton MR spectroscopy in infants with cerebral energy deficiency due to hypoxia and metabolic disorders.
    Acta radiologica (Stockholm, Sweden : 1987), 1998, Volume: 39, Issue:6

    Topics: Aspartic Acid; Basal Ganglia; Brain; Brain Diseases, Metabolic; Child, Preschool; Follow-Up Studies; Humans; Hypoxia; Infant; Lactic Acid; Magnetic Resonance Imaging; Metabolism, Inborn Errors; Methylamines; Oxidative Phosphorylation; Protons; Severity of Illness Index

1998
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease.
    American journal of medical genetics, 1989, Volume: 32, Issue:4

    Topics: Amidohydrolases; Aspartic Acid; Central Nervous System Diseases; Genes, Recessive; Humans; Metabolism, Inborn Errors; Nerve Degeneration

1989