phenytoin has been researched along with Hyperbilirubinemia, Hereditary in 2 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 | 2 (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 |
|---|---|
| Koch, MM | 1 |
| Lorenzini, I | 1 |
| Freddara, U | 1 |
| Jezequel, AM | 1 |
| Orlandi, F | 1 |
| Blaschke, TF | 1 |
| Berk, PD | 1 |
| Scharschmidt, BF | 1 |
| Guyther, JR | 1 |
| Vergalla, JM | 1 |
| Waggoner, JG | 1 |
2 other studies available for phenytoin and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
Type 2 Crigler-Najjar syndrome. Quantitation of ultrastructural data and evolution under therapy with phenytoin.
Topics: Crigler-Najjar Syndrome; Female; Humans; Hyperbilirubinemia, Hereditary; Liver; Liver Function Tests | 1978 |
Crigler-Najjar syndrome: an unusual course with development of neurologic damage at age eighteen.
Topics: Adolescent; Alkaline Phosphatase; Bilirubin; Brain Damage, Chronic; Brain Diseases; Carbon Monoxide; | 1974 |