LC-MS/MS chromatograms of A: the Cal06 calibrator (16 μM) and urine specimens from B: a healthy proband; C: a patient with ADSL deficiency; D: a patient with HGPRT deficiency; E: a patient with UPB1 deficiency; and F: a patient with APRT deficiency. All intensities (Y-axes) have been normalized to 1.5*108 cps for better comparability and have been plotted against retention time (X-axes). Analytes have been numbered as follows: 1. URA; 2. DHU; 3. Thy; 4. DHT; 5. BUP; 6. ADN; 7. Hypo; 8. ALLOP; 9. BUIB; 10. Xan; 11. DHA; 12. dAdo; 13. AICAr; 14. ADS; 15. HMU; 16. Oro; 17. dUrd; 18. THD; 19. PSU; 20. dIno; 21. dGui; 22. Ino; 23. Guo; 24. Ord; 25. SAICAr; 26. SAdo. The ISs have been marked by an asterisk (*) after the number of the respective u...
Recent findings suggest that inborn errors of pyrimidine catabolism are less rare than generally ass...
Background: the concentration of purine and pyrimidine metabolites in urine is useful marker of defe...
Background: A rapid and specific screening method for patients at risk of inherited disorders of pur...
Background and aimsInborn errors of purine and pyrimidine metabolism are a diverse group of disorder...
Background and aimsInborn errors of purine and pyrimidine metabolism are a diverse group of disorder...
BACKGROUND AND AIMS:Inborn errors of purine and pyrimidine metabolism are a diverse group of disorde...
Objectives: To develop a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to quantif...
BACKGROUND Clinical presentation and disease severity in disorders of purine and pyrimidine metaboli...
Liquid-chromatographic study of purine metabolism abnormalities in purine nucleoside phosphorylase d...
Background: Clinical presentation and disease severity in disorders of purine and pyrimidine metabol...
A rapid and specific screening method for patients at risk of inherited disorders of purine and pyri...
: Adenylosuccinate lyase (ADSL) deficiency is a rare autosomal recessive neurometabolic disorder tha...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Inborn errors of purine metabolism exhibit broad neurological, immunological, haematological and ren...
Aim: The aim of this study was to develop a high-throughput urine screening technique for adenylosuc...
Recent findings suggest that inborn errors of pyrimidine catabolism are less rare than generally ass...
Background: the concentration of purine and pyrimidine metabolites in urine is useful marker of defe...
Background: A rapid and specific screening method for patients at risk of inherited disorders of pur...
Background and aimsInborn errors of purine and pyrimidine metabolism are a diverse group of disorder...
Background and aimsInborn errors of purine and pyrimidine metabolism are a diverse group of disorder...
BACKGROUND AND AIMS:Inborn errors of purine and pyrimidine metabolism are a diverse group of disorde...
Objectives: To develop a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to quantif...
BACKGROUND Clinical presentation and disease severity in disorders of purine and pyrimidine metaboli...
Liquid-chromatographic study of purine metabolism abnormalities in purine nucleoside phosphorylase d...
Background: Clinical presentation and disease severity in disorders of purine and pyrimidine metabol...
A rapid and specific screening method for patients at risk of inherited disorders of purine and pyri...
: Adenylosuccinate lyase (ADSL) deficiency is a rare autosomal recessive neurometabolic disorder tha...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Inborn errors of purine metabolism exhibit broad neurological, immunological, haematological and ren...
Aim: The aim of this study was to develop a high-throughput urine screening technique for adenylosuc...
Recent findings suggest that inborn errors of pyrimidine catabolism are less rare than generally ass...
Background: the concentration of purine and pyrimidine metabolites in urine is useful marker of defe...
Background: A rapid and specific screening method for patients at risk of inherited disorders of pur...