ifosfamide 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 | 1 (100.00) | 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 |
---|---|
Goan, SR | 1 |
Fichtner, I | 1 |
Just, U | 1 |
Karawajew, L | 1 |
Schultze, W | 1 |
Krause, KP | 1 |
von Harsdorf, S | 1 |
von Schilling, C | 1 |
Herrmann, F | 1 |
1 other study available for ifosfamide and Severe Combined Immunodeficiency
Article | Year |
---|---|
The severe combined immunodeficient-human peripheral blood stem cell (SCID-huPBSC) mouse: a xenotransplant model for huPBSC-initiated hematopoiesis.
Topics: Adult; Animals; Antibody Formation; Antineoplastic Combined Chemotherapy Protocols; Bleomycin; Bone | 1995 |