dithionite has been researched along with Gaucher Disease in 1 studies
Dithionite: Dithionite. The dithionous acid ion and its salts.
Gaucher Disease: An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological 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 |
|---|---|
| Chambers, JP | 1 |
| Peters, SP | 1 |
| Glew, RH | 1 |
| Lee, RE | 1 |
| McCafferty, LR | 1 |
| Mercer, DW | 1 |
| Wenger, DA | 1 |
1 other study available for dithionite and Gaucher Disease
| Article | Year |
|---|---|
Multiple forms of acid phosphatase activity in Gaucher's disease.
Topics: Acid Phosphatase; Adult; Child; Child, Preschool; Chromatography, Ion Exchange; Dithionite; Fluoride | 1978 |