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n-caproylglycine and Fatty Liver with Encephalopathy

n-caproylglycine has been researched along with Fatty Liver with Encephalopathy in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (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
Coates, PM; Hale, DE; O'Shea, JJ; Rinaldo, P; Stanley, CA; Tanaka, K1

Other Studies

1 other study(ies) available for n-caproylglycine and Fatty Liver with Encephalopathy

ArticleYear
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