pyrimidine has been researched along with Adverse Drug Event in 3 studies
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 | 2 (66.67) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Hertz, DL; Sahai, V | 1 |
Blanco, C; García, MI; García-Alfonso, P; García-González, X; Grávalos, C; Iglesias, I; Longo, F; López-Fernández, LA; Martínez, J; Martínez, V; Pachón, V; Pellicer, M; Robles, L; Rueda, D; Salvador, S; Sanjurjo, M | 1 |
Altavilla, G; Barbara, C; Bordonaro, R; Butera, A; Cinieri, S; Cremolini, C; Crucitta, S; Danesi, R; De Braud, F; Del Re, M; Di Donato, S; Di Leo, A; Falcone, A; Latiano, TP; Loupakis, F; Maiello, E; Mazzotti, V; Michelucci, A; Morganti, R; Passardi, A; Pietrantonio, F; Pinto, C; Salvadori, S; Schirripa, M; Simi, P; Zamagni, C | 1 |
3 other study(ies) available for pyrimidine and Adverse Drug Event
Article | Year |
---|---|
Including DPYD on Cancer Genetic Panels to Prevent Fatal Fluoropyrimidine Toxicity.
Topics: Antineoplastic Combined Chemotherapy Protocols; Biomarkers; Drug-Related Side Effects and Adverse Reactions; Genetic Testing; Humans; Mutation; Neoplasms; Pharmacogenomic Variants; Polymorphism, Single Nucleotide; Prognosis; Pyrimidines; Treatment Outcome | 2020 |
Use of exome sequencing to determine the full profile of genetic variants in the fluoropyrimidine pathway in colorectal cancer patients affected by severe toxicity.
Topics: Adult; Aged; Aged, 80 and over; Antimetabolites, Antineoplastic; Biomarkers; Capecitabine; Colorectal Neoplasms; Drug-Related Side Effects and Adverse Reactions; Exome; Female; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Pyrimidines | 2017 |
DPYD*6 plays an important role in fluoropyrimidine toxicity in addition to DPYD*2A and c.2846A>T: a comprehensive analysis in 1254 patients.
Topics: Alleles; Cohort Studies; Dihydrouracil Dehydrogenase (NADP); Drug-Related Side Effects and Adverse Reactions; Female; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Pyrimidines | 2019 |