glycine has been researched along with Protoporphyria, Erythropoietic in 1 studies
Protoporphyria, Erythropoietic: An autosomal dominant porphyria that is due to a deficiency of FERROCHELATASE (heme synthetase) in both the LIVER and the BONE MARROW, the last enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include mainly neurological symptoms, rarely cutaneous lesions, and elevated levels of protoporphyrin and COPROPORPHYRINS in the feces.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| GRAY, CH | 1 |
| KULCZYCKA, A | 1 |
| NICHOLSON, DC | 1 |
| MAGNUS, IA | 1 |
| RIMINGTON, C | 1 |
1 other study available for glycine and Protoporphyria, Erythropoietic
| Article | Year |
|---|---|
ISOTOPE STUDIES ON A CASE OF ERYTHROPOIETIC PROTOPORPHYRIA.
Topics: Bilirubin; Blood Chemical Analysis; Body Fluids; Erythropoiesis; Feces; Glycine; Humans; Nitrogen; P | 1964 |