porphobilinogen has been researched along with Coproporphyria, Hereditary in 2 studies
Coproporphyria, Hereditary: An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.
| 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Grimes, R | 1 |
| Gilleece, Y | 1 |
| Appleby, T | 1 |
| Stockwell, S | 1 |
| Pinto-Sander, N | 1 |
| Sahabandu, T | 1 |
| Stein, P | 1 |
| Bradshaw, D | 1 |
| Ma, E | 1 |
| Mar, V | 1 |
| Varigos, G | 1 |
| Nicoll, A | 1 |
| Ross, G | 1 |
2 other studies available for porphobilinogen and Coproporphyria, Hereditary
| Article | Year |
|---|---|
A case of hereditary coproporphyria precipitated by efavirenz.
Topics: Abdominal Pain; Adult; Alkynes; Benzoxazines; Coproporphyria, Hereditary; Cyclopropanes; HIV Seropos | 2016 |
Haem arginate as effective maintenance therapy for hereditary coproporphyria.
Topics: Abdominal Pain; Adult; Arginine; Coproporphyria, Hereditary; Female; Heme; Humans; Photosensitivity | 2011 |