glycine has been researched along with Fatty Liver with Encephalopathy in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Forty had presented as Reye Syndrome, 9 as a Reye-like syndrome and 24 were sibs of decreased RS, sibs of RLS cases or sibs of infants who had died suddenly and without explanation where an autopsy revealed the presence of very heavy fatty infiltration of the liver." | 1.28 | The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders. ( Glasgow, JF; McKiernan, PJ; Moore, R; Robinson, PH, 1992) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Del Valle, JA | 1 |
| Garcia, MJ | 1 |
| Merinero, B | 1 |
| Pérez-Cerdá, C | 1 |
| Roman, F | 1 |
| Jimenez, A | 1 |
| Ugarte, M | 1 |
| Martínez-Pardo, M | 1 |
| Ludeña, C | 1 |
| Camarero, C | 1 |
| Truscott, RJ | 1 |
| Hick, L | 1 |
| Pullin, C | 1 |
| Halpern, B | 1 |
| Wilcken, B | 1 |
| Griffiths, H | 1 |
| Silink, M | 1 |
| Kilham, H | 1 |
| Grunseit, F | 1 |
| Glasgow, JF | 1 |
| Moore, R | 1 |
| Robinson, PH | 1 |
| McKiernan, PJ | 1 |
| Rinaldo, P | 1 |
| O'Shea, JJ | 1 |
| Coates, PM | 1 |
| Hale, DE | 1 |
| Stanley, CA | 1 |
| Tanaka, K | 1 |
4 other studies available for glycine and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome.
Topics: Acyl-CoA Dehydrogenases; Blood Glucose; Caprylates; Child, Preschool; Dicarboxylic Acids; Dietary Fa | 1984 |
Dicarboxylic aciduria: the response to fasting.
Topics: Adipates; Child; Chromatography, Gas; Dicarboxylic Acids; Fasting; Glycine; Humans; Male; Reye Syndr | 1979 |
The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Adolescent; Child; Child, Preschool; Glycine; Hippu | 1992 |
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Child; Child, Preschool; Diagnosis, Differential; D | 1988 |