thymidine has been researched along with Dihydropyrimidine Dehydrogenase Deficiency in 1 studies
Dihydropyrimidine Dehydrogenase Deficiency: An autosomal recessive disorder affecting DIHYDROPYRIMIDINE DEHYDROGENASE and causing familial pyrimidinemia. It is characterized by thymine-uraciluria in homozygous deficient patients. Even a partial deficiency in the enzyme leaves individuals at risk for developing severe 5-FLUOROURACIL-associated toxicity.
| 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 |
|---|---|
| Liu, N | 1 |
| Sun, Q | 1 |
1 other study available for thymidine and Dihydropyrimidine Dehydrogenase Deficiency
| Article | Year |
|---|---|
Quantitation of Pyrimidine in Urine by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry.
Topics: Biomarkers; Chromatography, Liquid; Dihydropyrimidine Dehydrogenase Deficiency; Humans; Pyrimidines; | 2022 |