eosine yellowish-(ys) has been researched along with Glucosephosphate Dehydrogenase Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 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 | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Liao, L; Lin, F; Wu, Y | 1 |
| Meerhof, LJ; Roos, D | 1 |
1 review(s) available for eosine yellowish-(ys) and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
The diagnostic protocol for hereditary spherocytosis-2021 update.
Topics: Anemia, Hemolytic, Autoimmune; Diagnosis, Differential; Diagnostic Errors; Eosine Yellowish-(YS); Erythrocyte Indices; Glucosephosphate Dehydrogenase Deficiency; Humans; Mutation; Practice Guidelines as Topic; Spherocytosis, Hereditary | 2021 |
1 other study(ies) available for eosine yellowish-(ys) and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Heterogeneity in chronic granulomatous disease detected with an improved nitroblue tetrazolium slide test.
Topics: Cytochrome b Group; Eosine Yellowish-(YS); Female; Glucosephosphate Dehydrogenase Deficiency; Granulomatous Disease, Chronic; Humans; Leukocytes; Male; Methylene Blue; Nitroblue Tetrazolium; Oxygen Consumption; Pedigree; Phagocytosis; Staining and Labeling; Superoxides; Tetrazolium Salts | 1986 |