Uridine

aconitate decarboxylase 1 ; Homo sapiens







5 Article(s)
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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