hydroxyurea has been researched along with Porphyrias, Hepatic in 1 studies
Porphyrias, Hepatic: A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Neeleman, RA | 1 |
| van Beers, EJ | 1 |
| Friesema, EC | 1 |
| Koole-Lesuis, R | 1 |
| van der Pol, WL | 1 |
| Wilson, JHP | 1 |
| Langendonk, JG | 1 |
1 other study available for hydroxyurea and Porphyrias, Hepatic
| Article | Year |
|---|---|
Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis.
Topics: Adult; Erythroid Cells; Heme; Humans; Hydroxyurea; Infant, Newborn; Male; Nucleic Acid Synthesis Inh | 2019 |