porphobilinogen has been researched along with Porphyria, Variegate in 1 studies
Porphyria, Variegate: An autosomal dominant porphyria that is due to a deficiency of protoporphyrinogen oxidase (EC 1.3.3.4) in the LIVER, the seventh 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, COPROPORPHYRINS and protoporphyrinogen.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Di Pierro, E | 1 |
| Ventura, P | 1 |
| Brancaleoni, V | 1 |
| Moriondo, V | 1 |
| Marchini, S | 1 |
| Tavazzi, D | 1 |
| Nascimbeni, F | 1 |
| Ferrari, MC | 1 |
| Rocchi, E | 1 |
| Cappellini, MD | 1 |
1 other study available for porphobilinogen and Porphyria, Variegate
| Article | Year |
|---|---|
Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy.
Topics: Adult; Aged; Aminolevulinic Acid; Female; Flavoproteins; Genetic Association Studies; Genotype; Huma | 2009 |