pyrimidine has been researched along with Intellectual Disability in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alhaddad, B; Botto, LD; Chen, MA; Colombo, R; Coughlin, CR; Descartes, M; Grűnewald, S; Kluijtmans, LA; Maranda, B; Mills, PB; Pai, EF; Pitt, J; Pontoglio, A; Potente, C; Rodenburg, R; Sampath, S; Tiller, GE; Wevers, RA; Wortmann, SB; Yuzyuk, T | 1 |
| DELLAPORTA, P; MAIOLO, AT; ROSSELLA, E | 1 |
| Connolly, GP | 1 |
| Aukett, A; Baaske, H; Dobritzsch, D; Duley, JA; Haasjes, J; Hein, G; Kalhoff, H; Kirk, JM; Lindqvist, Y; Maropoulos, GD; Meinsma, R; Nowaczyk, MJ; van Gennip, AH; van Kuilenburg, AB; Ward, KP; Waterham, HR | 1 |
4 other study(ies) available for pyrimidine and Intellectual Disability
| Article | Year |
|---|---|
Mild orotic aciduria in UMPS heterozygotes: a metabolic finding without clinical consequences.
Topics: Anemia, Megaloblastic; Child; Child, Preschool; Female; Heterozygote; Humans; Infant; Intellectual Disability; Male; Multienzyme Complexes; Mutation; Orotate Phosphoribosyltransferase; Orotic Acid; Orotidine-5'-Phosphate Decarboxylase; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines; Urea Cycle Disorders, Inborn; Uridine | 2017 |
[BEHAVIOR OF CEREBRAL BLOOD FLOW AND METABOLISM AFTER ADMINISTRATION OF 2,6 BIS-(DIETHANOLAMINO)-4,8 DIPIPERIDINO-PYRIMIDO(5,4 D)-PYRIMIDINE].
Topics: Alcoholism; Blood Flow Velocity; Blood Gas Analysis; Brain; Carbohydrate Metabolism; Cerebrovascular Circulation; Dipyridamole; Intellectual Disability; Metabolism; Pyrimidines; Schizophrenia | 1963 |
Abnormal pyrimidine metabolism is the basis of some neurological diseases.
Topics: Autistic Disorder; Central Nervous System Diseases; Humans; Intellectual Disability; Pyrimidines; Seizures | 1998 |
Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure.
Topics: Age of Onset; Amino Acids; Animals; Cells, Cultured; Child, Preschool; Crystallography, X-Ray; Dihydrouracil Dehydrogenase (NADP); Electron Transport; Exons; Fibroblasts; Fluorouracil; Gene Deletion; Genotype; Granulocytes; Humans; Infant; Infant, Newborn; Intellectual Disability; Leukocytes, Mononuclear; Models, Molecular; Motor Skills Disorders; Mutation; Mutation, Missense; Oxidoreductases; Phenotype; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Pyrimidines; Swine; Thymine; Uracil | 2002 |