3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11675655&form=6&db=m beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urine. unassigned - 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11746386&form=6&db=m 3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesis. causal interaction,unassigned 3,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11783492&form=6&db=m Confirmation of the enzyme defect in the first case of beta-ureidopropionase deficiency. Beta-alanine deficiency. causal interaction,unassigned 4,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11804209&form=6&db=m Detection of beta-ureidopropionase deficiency with HPLC-electrospray tandem mass spectrometry and confirmation of the defect at the enzyme level. causal interaction,diagnostic usage,unassigned 3,3,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12271438&form=6&db=m Screening and diagnosis of beta-ureidopropionase deficiency by gas chromatographic/mass spectrometric analysis of urine. causal interaction,diagnostic usage,unassigned 4,4,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12450676&form=6&db=m Diagnosis and monitoring of inborn errors of metabolism using urease-pretreatment of urine, isotope dilution, and gas chromatography-mass spectrometry. causal interaction,diagnostic usage,unassigned 3,1,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15385443&form=6&db=m beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities. causal interaction,diagnostic usage,unassigned 4,3,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16417553&form=6&db=m beta-Ureidopropionase Deficiency Presenting with Febrile Status Epilepticus. causal interaction,unassigned 4,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16541364&form=6&db=m Clinical Findings and a Therapeutic Trial in the First Patient with beta-Ureidopropionase Deficiency. causal interaction,therapeutic application,unassigned 4,4,0 3.5.1.6 beta-ureidopropionase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17065070&form=6&db=m Genetic analysis of the first 4 patients with beta-ureidopropionase deficiency. causal interaction,diagnostic usage,unassigned 4,2,0