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homocarnosine and Amino Acid Metabolism Disorders, Inborn

homocarnosine has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gibson, KM; Pearl, PL1
Gibson, KM; Jaeken, J; Jakobs, C1
Hamajima, N; Wada, Y1

Reviews

3 review(s) available for homocarnosine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Clinical aspects of the disorders of GABA metabolism in children.
    Current opinion in neurology, 2004, Volume: 17, Issue:2

    Topics: 4-Aminobutyrate Transaminase; Aldehyde Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Brain; Carnosine; Child; Developmental Disabilities; Diagnosis, Differential; Epilepsy; gamma-Aminobutyric Acid; Glutamate Decarboxylase; Humans; Magnetic Resonance Imaging; Phenotype; Pyridoxal Phosphate; Pyridoxine; Succinate-Semialdehyde Dehydrogenase

2004
Inherited disorders of GABA metabolism.
    Journal of inherited metabolic disease, 1993, Volume: 16, Issue:4

    Topics: 4-Aminobutyrate Transaminase; Aldehyde Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Carnosine; Dipeptidases; gamma-Aminobutyric Acid; Glutamate Decarboxylase; Humans; Succinate-Semialdehyde Dehydrogenase

1993
[Serum carnosinase deficiency and homocarnosinosis].
    Ryoikibetsu shokogun shirizu, 1998, Issue:18 Pt 1

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Carnosine; Diagnosis, Differential; Dipeptidases; Humans; Prognosis

1998