• Absence of oroticaciduria in adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency
• Conditional disruption of hepatic carbamoyl phosphate synthetase 1 in mice results in hyperammonemia without orotic aciduria and can be corrected by liver-directed gene therapy
• Dietary feedback regulation of purine and pyrimidine biosynthesis in man
• Effect of 6-azauridine on de novo pyrimidine biosynthesis in cultured Ehrlich ascites cells. Orotate inhibition of dihydroorotase and dihydroorotate dehydrogenase
• Isolated Orotic Aciduria in an 11-Year-Old Boy
• Megaloblastic anemia--a rare cause
• Mild orotic aciduria in UMPS heterozygotes: a metabolic finding without clinical consequences
• Novel mutation in UMPS gene leads to false positive result of DUMPS (genetic disorder) in buffaloes: need for gene sequencing before confirming results of RFLP in new species
• Orotic aciduria and uridine monophosphate synthase: a reappraisal
• Pseudouridine metabolism. II. Urinary excretion in gout, psoriasis, leukemia, and heterozygous oroticaciduria
• Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovine citrullinaemia, and factor XI deficiency in Holstein cows reared in Turkey
• Studies on congenital orotic aciduria: comparison of orotic acid metabolism in microorganisms
• The uricosuria and orotic aciduria induced by 6-azauridine
• Urinary oxipurinol-1-riboside excretion and allopurinol-induced oroticaciduria
• Use of intact erythrocytes in the diagnosis of inherited purine and pyrimidine disorders