dihydroxyacetone has been researched along with Glycogen Storage Disease in 1 studies
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| 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 |
|---|---|
| GADIOT, JM | 1 |
| LEHR, CF | 1 |
1 other study available for dihydroxyacetone and Glycogen Storage Disease
| Article | Year |
|---|---|
[GLYCOGENOSIS TYPE III IN DIZYGOTIC TWINS, WITH SPECIAL REFERENCE TO THE EFFECT OF DIHYDROXYACETONE].
Topics: Acetone; Blood Chemical Analysis; Child; Dihydroxyacetone; Dinitrophenols; Diseases in Twins; Glycog | 1964 |