hydroxyurea has been researched along with Severe Combined Immunodeficiency in 1 studies
Severe Combined Immunodeficiency: Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 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 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tsui, M | 1 |
| Min, W | 1 |
| Ng, S | 1 |
| Dobbs, K | 1 |
| Notarangelo, LD | 1 |
| Dror, Y | 1 |
| Grunebaum, E | 1 |
1 other study available for hydroxyurea and Severe Combined Immunodeficiency
| Article | Year |
|---|---|
The Use of Induced Pluripotent Stem Cells to Study the Effects of Adenosine Deaminase Deficiency on Human Neutrophil Development.
Topics: Adenosine Deaminase; Agammaglobulinemia; Cells, Cultured; Embryoid Bodies; Fibroblasts; Granulocytes | 2021 |