tyrosine has been researched along with Crigler Najjar Syndrome in 2 studies
| 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 |
|---|---|
| Bamba, T; Doida, Y; Fujiyama, Y; Sato, H; Yamamoto, K | 1 |
| Mowat, AP | 1 |
2 other study(ies) available for tyrosine and Crigler Najjar Syndrome
| Article | Year |
|---|---|
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 Activation; Gilbert Disease; Glucuronosyltransferase; Glycine; Homozygote; Humans; Mutation, Missense; Phenotype; Transfection; Tyrosine | 1998 |
Liver disorders in children: the indications for liver replacement in parenchymal and metabolic diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Budd-Chiari Syndrome; Child; Cholangitis; Crigler-Najjar Syndrome; Hepatitis, Chronic; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Liver Diseases; Liver Transplantation; Porphyrias; Tyrosine | 1987 |