Page last updated: 2024-10-21

urea and CBS Deficiency

urea has been researched along with CBS Deficiency in 12 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-199012 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Nyhan, WL1
Wellner, D1
Meister, A1
Snyderman, SE1
Griffiths, R1
Tudball, N1
Omenn, GS1
Irons, M1
Levy, HL1
Sautter, H1
Schroeder, W1
Naumann, G1
Martin, JJ2
Schlote, W2
Hooft, C1
Carton, D1
Menkes, JH1
Heathcote, JG1
Davies, DM1
Haworth, C1
Oliver, RW1

Reviews

5 reviews available for urea and CBS Deficiency

ArticleYear
Understanding inherited metabolic disease.
    Clinical symposia (Summit, N.J. : 1957), 1980, Volume: 32, Issue:5

    Topics: Amniocentesis; Carboxy-Lyases; Female; Genetic Carrier Screening; Homocystinuria; Humans; Infant, Ne

1980
A survey of inborn errors of amino acid metabolism and transport in man.
    Annual review of biochemistry, 1981, Volume: 50

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport

1981
The dietary therapy of inherited metabolic disease.
    Progress in food & nutrition science, 1975, Volume: 1, Issue:7-8

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C

1975
Inborn errors of metabolism: clues to understanding human behavioral disorders.
    Behavior genetics, 1976, Volume: 6, Issue:3

    Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter

1976
Metabolic syndromes with dermatologic manifestations.
    Clinical reviews in allergy, 1986, Volume: 4, Issue:1

    Topics: Albinism; Alkaptonuria; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biotinid

1986

Other Studies

7 other studies available for urea and CBS Deficiency

ArticleYear
The molecular defect in a case of (cystathionine beta-synthase)-deficient homocystinuria.
    European journal of biochemistry, 1977, Apr-01, Volume: 74, Issue:2

    Topics: Cross Reactions; Cystathionine beta-Synthase; Fibroblasts; Homocystinuria; Humans; Hydro-Lyases; Imm

1977
[Results of surgical treatment in dislocated lenses. I. Aspiration of dislocated lenses in children and in young persons (author's transl)].
    Klinische Monatsblatter fur Augenheilkunde, 1974, Volume: 165, Issue:3

    Topics: Adolescent; Adult; Child; Child, Preschool; Female; Homocystinuria; Humans; Intraocular Pressure; La

1974
Neuropathological study of aminoacidurias.
    Monographs in human genetics, 1972, Volume: 6

    Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Central Nervous System; Cystathionine; Female; Gl

1972
Pediatric clinical aspects of aminoacidopathies.
    Monographs in human genetics, 1972, Volume: 6

    Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Arginine; Child; Child, Preschool; Female; Homocy

1972
Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.
    Journal of the neurological sciences, 1972, Volume: 15, Issue:1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Central Nervous System; Chi

1972
Disorders of amino acid metabolism--1971.
    California medicine, 1971, Volume: 115, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease;

1971
An improved technique for the analysis of amino acids and related compounds on thin layers of cellulose. IV. The quantitative determination of amino acids in urine.
    Journal of chromatography, 1971, Mar-03, Volume: 55, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Autoanalysis; Cellulose; Child; Chromatography, Ion Exchange;

1971