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n-carbamoyl-beta-alanine and Ornithine Carbamoyltransferase Deficiency Disease

n-carbamoyl-beta-alanine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 2 studies

N-carbamoyl-beta-alanine: RN given refers to parent cpd
N-carbamoyl-beta-alanine : A beta-alanine derivative that is propionic acid bearing a ureido group at position 3.

Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Schmidt, C1
Hofmann, U1
Kohlmüller, D1
Mürdter, T1
Zanger, UM1
Schwab, M1
Hoffmann, GF1
Inoue, Y1
Ohkura, T1
Matsumoto, I1
Rudewicz, PJ1

Other Studies

2 other studies available for n-carbamoyl-beta-alanine and Ornithine Carbamoyltransferase Deficiency Disease

ArticleYear
Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high-pressure liquid chromatography-electrospray ionization tandem mass spectrometry.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6

    Topics: Adolescent; beta-Alanine; Child; Child, Preschool; Chromatography, High Pressure Liquid; Dihydropyri

2005
Fast atom bombardment tandem mass spectrometric analysis of N-carbamoylamino acids.
    Biological mass spectrometry, 1991, Volume: 20, Issue:10

    Topics: Amino Acids; Aspartic Acid; beta-Alanine; Carbamates; Humans; Ornithine Carbamoyltransferase Deficie

1991