Compounds > n-caproylglycine
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n-caproylglycine and 3-phenylpropionylglycine

n-caproylglycine has been researched along with 3-phenylpropionylglycine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bennett, MJ; Bhala, A; Hale, DE; Poirier, SF; Ragni, MC; Willi, SM1
O'Shea, JJ; Rinaldo, P; Tanaka, K; Welch, RD1
Coates, PM; Hale, DE; O'Shea, JJ; Rinaldo, P; Stanley, CA; Tanaka, K1
Bennett, MJ; Ostfeld, RJ; Ragni, MC; Santer, R; Schmidt-Sommerfeld, E1
Bennett, MJ; Bhala, A; Hale, DE; McGowan, KL1

Other Studies

5 other study(ies) available for n-caproylglycine and 3-phenylpropionylglycine

ArticleYear
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency.
    Clinical chemistry, 1992, Volume: 38, Issue:2

    Topics: Acyl-CoA Dehydrogenases; Enterobacteriaceae; Feces; Female; Glycine; Humans; Infant; Infant, Newborn; Intestines; Neonatal Screening; Phenylpropionates

1992
Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring.
    Biomedical & environmental mass spectrometry, 1989, Volume: 18, Issue:7

    Topics: Chemical Phenomena; Chemistry; Child; Chromatography, Ion Exchange; Dicarboxylic Acids; Gas Chromatography-Mass Spectrometry; Glycine; Humans

1989
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
    The New England journal of medicine, 1988, Nov-17, Volume: 319, Issue:20

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Child; Child, Preschool; Diagnosis, Differential; Dicarboxylic Acids; Glycine; Humans; Infant; Infant, Newborn; Methods; Radioisotope Dilution Technique; Retrospective Studies; Reye Syndrome; Sudden Infant Death

1988
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots.
    Annals of clinical biochemistry, 1994, Volume: 31 ( Pt 1)

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Child, Preschool; Decanoic Acids; Fatty Acids; Fatty Acids, Monounsaturated; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Infant; Infant, Newborn; Neonatal Screening; Reference Values; Sensitivity and Specificity

1994
Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.
    The Journal of pediatrics, 1993, Volume: 122, Issue:1

    Topics: Acyl-CoA Dehydrogenase; Adult; Anti-Bacterial Agents; Bacteria, Anaerobic; Caproates; Child; Clostridium; Fatty Acid Desaturases; Glycine; Humans; Infant; Phenylalanine; Phenylpropionates

1993