glycine has been researched along with Constitutional Liver Dysfunction in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "2." | 1.26 | Sources of bile pigment overproduction in Gilbert's syndrome: studies with non-radioactive bilirubin kinetics and with delta-[3,5-3H]aminolaevulinic acid and [2-14C]glycine. ( Cremonini, C; Gozzi, C; Piaggi, V; Ventura, E; Zeneroli, ML, 1982) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Zeneroli, ML | 1 |
| Piaggi, V | 1 |
| Cremonini, C | 1 |
| Gozzi, C | 1 |
| Ventura, E | 1 |
| Yamamoto, K | 1 |
| Sato, H | 1 |
| Fujiyama, Y | 1 |
| Doida, Y | 1 |
| Bamba, T | 1 |
2 other studies available for glycine and Constitutional Liver Dysfunction
| Article | Year |
|---|---|
Sources of bile pigment overproduction in Gilbert's syndrome: studies with non-radioactive bilirubin kinetics and with delta-[3,5-3H]aminolaevulinic acid and [2-14C]glycine.
Topics: Adolescent; Adult; Aminolevulinic Acid; Bilirubin; Female; Gilbert Disease; Glycine; Humans; Hyperbi | 1982 |
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.
Topics: Animals; Arginine; Aspartic Acid; Blotting, Western; COS Cells; Crigler-Najjar Syndrome; Enzyme Acti | 1998 |