5 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33249780 | Triacetyluridine treats epileptic encephalopathy from CAD mutations: a case report and review. | 2021 Jan | 1 |
2 | 32117025 | A Patient With CAD Deficiency Responsive to Uridine and Literature Review. | 2020 | 1 |
3 | 32461667 | Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy. | 2020 Oct | 6 |
4 | 32720728 | Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene. | 2020 Nov | 1 |
5 | 32820246 | Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementation. | 2020 Oct | 1 |