Page last updated: 2024-09-03

octanoylcarnitine and n-caproylglycine

octanoylcarnitine has been researched along with n-caproylglycine in 1 studies

Compound Research Comparison

Studies (octanoylcarnitine)	Trials (octanoylcarnitine)	Recent Studies (post-2010) (octanoylcarnitine)	Studies (n-caproylglycine)	Trials (n-caproylglycine)	Recent Studies (post-2010) (n-caproylglycine)
86	1	30	19	1	1

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gavrilov, D; Highsmith, WE; Matern, D; McHugh, D; Oglesbee, D; Raymond, K; Rinaldo, P; Smith, EH; Thomas, C; Tortorelli, S	1

Other Studies

1 other study(ies) available for octanoylcarnitine and n-caproylglycine

Article	Year
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. Molecular genetics and metabolism, 2010, Volume: 100, Issue:3 Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Alleles; Carnitine; Child; Child, Preschool; DNA Mutational Analysis; Exons; Genetic Association Studies; Genetic Carrier Screening; Genetic Variation; Genotype; Glycine; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Middle Aged; Mutation; Mutation, Missense; Neonatal Screening; Polymorphism, Single Nucleotide; Young Adult	2010

Article

Year

Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing.

Molecular genetics and metabolism, 2010, Volume: 100, Issue:3

Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Alleles; Carnitine; Child; Child, Preschool; DNA Mutational Analysis; Exons; Genetic Association Studies; Genetic Carrier Screening; Genetic Variation; Genotype; Glycine; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Middle Aged; Mutation; Mutation, Missense; Neonatal Screening; Polymorphism, Single Nucleotide; Young Adult

2010