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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 3.5.1.6Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.6Phenylketonurias 17467347 Noninvasive human metabolome analysis for differential diagnosis of inborn errors of metabolism. causal interaction
unassigned
3
0
Show all pathways known for 3.5.1.6Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.6Propionic Acidemia 11746386 3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesis. causal interaction
unassigned
3
0
Show all pathways known for 3.5.1.6Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.6Propionic Acidemia 12450676 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
Show all pathways known for 3.5.1.6Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.6Protein Deficiency 1802976 Effect of dietary protein on pyrimidine-metabolizing enzymes in rats. causal interaction
unassigned
1
0
Show all pathways known for 3.5.1.6Display the word mapDisplay the reaction diagram Show all sequences 3.5.1.6Status Epilepticus 16417553 beta-Ureidopropionase Deficiency Presenting with Febrile Status Epilepticus. causal interaction
unassigned
4
0
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