glycine has been researched along with Lipid Metabolism, Inborn Error in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (50.00) | 18.7374 |
| 1990's | 3 (25.00) | 18.2507 |
| 2000's | 1 (8.33) | 29.6817 |
| 2010's | 2 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fukao, T | 1 |
| Akiba, K | 1 |
| Goto, M | 1 |
| Kuwayama, N | 1 |
| Morita, M | 1 |
| Hori, T | 1 |
| Aoyama, Y | 1 |
| Venkatesan, R | 1 |
| Wierenga, R | 1 |
| Moriyama, Y | 1 |
| Hashimoto, T | 1 |
| Usuda, N | 1 |
| Murayama, K | 1 |
| Ohtake, A | 1 |
| Hasegawa, Y | 2 |
| Shigematsu, Y | 1 |
| Smith, EH | 1 |
| Thomas, C | 1 |
| McHugh, D | 1 |
| Gavrilov, D | 1 |
| Raymond, K | 1 |
| Rinaldo, P | 2 |
| Tortorelli, S | 1 |
| Matern, D | 1 |
| Highsmith, WE | 1 |
| Oglesbee, D | 1 |
| Gregersen, N | 2 |
| Rosleff, F | 1 |
| Kølvraa, S | 2 |
| Hobolth, N | 1 |
| Rasmussen, K | 1 |
| Lauritzen, R | 1 |
| Martinez, G | 1 |
| Garcia-Lozano, JR | 1 |
| Ribes, A | 1 |
| Maldonado, MD | 1 |
| Baldellou, A | 1 |
| de Pablo, R | 1 |
| Nuñez-Roldan, A | 1 |
| Kimura, M | 1 |
| Yamaguchi, S | 1 |
| Costa, CG | 1 |
| Guérand, WS | 1 |
| Struys, EA | 1 |
| Holwerda, U | 1 |
| ten Brink, HJ | 1 |
| Tavares de Almeida, I | 1 |
| Duran, M | 1 |
| Jakobs, C | 1 |
| Tanaka, K | 2 |
| Mantagos, S | 1 |
| Genel, M | 1 |
| Seashore, MR | 1 |
| Billings, BA | 1 |
| Baretz, BH | 1 |
| Brady, RO | 1 |
| Bennett, MJ | 1 |
| Pollitt, RJ | 1 |
| Taitz, LS | 1 |
| Variend, S | 1 |
| O'Shea, JJ | 1 |
| Goodman, SI | 1 |
| Miller, LV | 1 |
| Fennessey, PV | 1 |
| Whelan, DT | 1 |
| Hill, RE | 1 |
| Mortensen, PB | 1 |
| Minder, FC | 1 |
| Dubach, UC | 1 |
| Antener, I | 1 |
12 other studies available for glycine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acetyltransferase; Base Sequence; Carnitine; Child; D | 2014 |
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Alleles; Carnitine; Child; Child, Preschool; DNA Mutation | 2010 |
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases.
Topics: Adipates; Caproates; Caprylates; Child, Preschool; Chromatography, Gas; Decanoic Acids; Dicarboxylic | 1980 |
High risk of medium chain acyl-coenzyme A dehydrogenase deficiency among gypsies.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Alanine; Alleles; Gene Frequency; Genetic Carrier S | 1998 |
Screening for fatty acid beta oxidation disorders. Acylglycine analysis by electron impact ionization gas chromatography-mass spectrometry.
Topics: Dicarboxylic Acids; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Lipid Metabolism, Inborn | 1999 |
Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Child; Child, Preschool; Fatty Acid Desaturases; Gas Chroma | 2000 |
New defect in fatty-acid metabolism with hypoglycemia and organic aciduria.
Topics: Adipates; Child, Preschool; Fatty Acids; Female; Glycine; Humans; Hypoglycemia; Lipid Metabolism, In | 1977 |
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors | 1976 |
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Family; Family Health; Female; Glycine; Humans; Inf | 1990 |
Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Acylation; Biomarkers; Carnitine; Glycine; Humans; | 1989 |
Acyl-CoA: glycine N-acyltransferase: in vitro studies on the glycine conjugation of straight- and branched-chained acyl-CoA esters in human liver.
Topics: Acyl Coenzyme A; Acyltransferases; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Fatty Acid | 1986 |
[Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Deafness; Dw | 1965 |