ifosfamide has been researched along with Cerebro-Oculo-Renal Syndrome in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"The renal Fanconi syndrome is a defect of proximal tubular function causing aminoaciduria and low-molecular-weight proteinuria." | 1.34 | Combined proteomic and metabonomic studies in three genetic forms of the renal Fanconi syndrome. ( Capasso, G; Cutillas, PR; Holmes, E; Maher, AD; Nicholson, JK; Norden, AW; Unwin, RJ; Vilasi, A; Zirah, SF, 2007) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Vilasi, A | 1 |
Cutillas, PR | 1 |
Maher, AD | 1 |
Zirah, SF | 1 |
Capasso, G | 1 |
Norden, AW | 1 |
Holmes, E | 1 |
Nicholson, JK | 1 |
Unwin, RJ | 1 |
1 other study available for ifosfamide and Cerebro-Oculo-Renal Syndrome
Article | Year |
---|---|
Combined proteomic and metabonomic studies in three genetic forms of the renal Fanconi syndrome.
Topics: Adult; Antineoplastic Agents, Alkylating; Chloride Channels; DNA Fingerprinting; Fanconi Syndrome; F | 2007 |