tryptophan has been researched along with Hyperbilirubinemia, Hereditary in 2 studies
| 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 |
|---|---|
| Akagi, N; Kubo, Y; Maeda, T; Morita, M; Morita, S; Ogawa, Y; Sawada, A; Yamamoto, Y; Yoshida, S | 1 |
| Tabolin, VA | 1 |
2 other study(ies) available for tryptophan 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; Pyridoxal; Radionuclide Imaging; Syndrome; Technetium; Technetium Tc 99m Diethyl-iminodiacetic Acid; Tryptophan | 1985 |
[Metabolic disorders, their early diagnosis and therapy in newborn infants].
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Cystic Fibrosis; Fanconi Syndrome; Humans; Hyperbilirubinemia, Hereditary; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Jaundice, Neonatal; Malabsorption Syndromes; Neurologic Manifestations; Phenylketonurias; Tryptophan | 1973 |