uridine has been researched along with Developmental Disabilities in 2 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 | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berry, G; Ejaz, A; Jayakar, P; Koh, HY; Mahida, S; McGraw, CM; Poduri, A; Resnick, T; Rodan, L; Sankaran, VG; Schwartz, MA; Taylor, A | 1 |
| Alhaddad, B; Bader, I; Betzler, C; Bierau, J; Coene, KL; Distelmaier, F; Haack, TB; Holzhacker, M; Koch, J; Kovacs-Nagy, R; Leiz, S; Mayr, JA; Meitinger, T; Polster, T; Prokisch, H; Rauscher, C; Sperl, W; Strom, TM; Venselaar, H; Wevers, RA; Wortmann, SB | 1 |
2 other study(ies) available for uridine and Developmental Disabilities
| Article | Year |
|---|---|
Uridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings.
Topics: Aspartate Carbamoyltransferase; Atrophy; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing); Cerebellar Diseases; Child; Child, Preschool; Developmental Disabilities; Dihydroorotase; Disease Progression; Drug Resistant Epilepsy; Female; Humans; Male; Pedigree; Siblings; Uridine | 2021 |
CAD mutations and uridine-responsive epileptic encephalopathy.
Topics: Anemia; Aspartate Carbamoyltransferase; Brain; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing); Child; Child, Preschool; Developmental Disabilities; Dihydroorotase; DNA Mutational Analysis; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Mutation; Spasms, Infantile; Uridine | 2017 |