pyridoxal has been researched along with Hyperbilirubinemia, Hereditary in 1 studies
Hyperbilirubinemia, Hereditary: Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Yoshida, S | 1 |
| Sawada, A | 1 |
| Ogawa, Y | 2 |
| Morita, S | 1 |
| Morita, M | 1 |
| Yamamoto, Y | 1 |
| Maeda, T | 1 |
| Akagi, N | 1 |
| Kubo, Y | 1 |
1 other study available for pyridoxal and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
[Hepatobiliary scintigraphy with Tc-99m-PMT in a case of Rotor's disease. Comparison with the image of Tc-99m E-HIDA].
Topics: Female; Humans; Hyperbilirubinemia, Hereditary; Imino Acids; Middle Aged; Organotechnetium Compounds | 1985 |