sarcosine has been researched along with Metabolism, Inborn Errors in 6 studies
cocobetaine: N-alkyl-betaine; cause of shampoo dermatitis
Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.
| Excerpt | Relevance | Reference |
|---|---|---|
| "When amino acids were infused at a rate of 4 g/kg/day, an infant with hypoglycemia, metabolic acidemia and chronic regurgitation showed hypersarcosinemia and excreted abnormal amounts of sarcosine, isovalerylglycine, isobutyrylglycine, alpha-methylbutyrylglycine, and beta-hydroxyisovaleric, glutaric, alpha-hydroxyglutaric, methylsuccinic, and alpha-hydroxyisobutyric acids in urine." | 3.66 | Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. ( Fennessey, PV; Goodman, SI; Mace, JW; McCabe, ER, 1980) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lever, M | 1 |
| McEntyre, CJ | 1 |
| George, PM | 1 |
| Chambers, ST | 1 |
| Goodman, SI | 1 |
| McCabe, ER | 1 |
| Fennessey, PV | 1 |
| Mace, JW | 1 |
| Allen, RH | 1 |
| Stabler, SP | 1 |
| Lindenbaum, J | 1 |
| Moolenaar, SH | 2 |
| Poggi-Bach, J | 2 |
| Engelke, UF | 2 |
| Corstiaensen, JM | 1 |
| Heerschap, A | 1 |
| de Jong, JG | 1 |
| Binzak, BA | 2 |
| Vockley, J | 2 |
| Wevers, RA | 2 |
| Lee, YM | 1 |
| Hwu, WL | 1 |
| Hoard, HM | 1 |
| Vockley, JG | 1 |
| Jellum, E | 1 |
6 other studies available for sarcosine and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Is N,N-dimethylglycine N-oxide a choline and betaine metabolite?
Topics: Adult; Betaine; Choline; Humans; Male; Metabolism, Inborn Errors; Methylamines; Sarcosine; Young Adu | 2017 |
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein.
Topics: Acids; Acyl-CoA Dehydrogenases; Amino Acids; Flavoproteins; Glutarates; Humans; Hypoglycemia; Infant | 1980 |
Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism.
Topics: Adolescent; Adult; Aged; Animals; Betaine; Betaine-Homocysteine S-Methyltransferase; Chromatography; | 1993 |
Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study.
Topics: Adult; Dimethylglycine Dehydrogenase; Gas Chromatography-Mass Spectrometry; Humans; Magnetic Resonan | 1999 |
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.
Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Black People; Blotting, Western; | 2001 |
Chromatography for diagnosis of metabolic diseases.
Topics: Amino Acids; Child, Preschool; Chromatography, Ion Exchange; Female; Gas Chromatography-Mass Spectro | 1988 |