β-Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine-Reference-Cited by-同舟云学术

β-Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine

Published:2001-10-18 Issue:5 Volume:46 Page:1014-1017
ISSN:0740-3194
Container-title:Magnetic Resonance in Medicine
language:en
Short-container-title:Magn. Reson. Med.

Author:

Moolenaar Sytske H.,Göhlich-Ratmann Gudrun,Engelke Udo F.H.,Spraul Manfred,Humpfer Eberhard,Dvortsak Peter,Voit Thomas,Hoffmann Georg F.,Bräutigam Christa,van Kuilenburg André B.,van Gennip Albert,Vreken Peter,Wevers Ron A.

Funder

Fonds Vertrokken Klinisch Chemici Nijmegen

Publisher

Wiley

Subject

Radiology Nuclear Medicine and imaging

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4. Proton NMR spectroscopic analysis of multiple acyl-CoA dehydrogenase deficiency-capacity of the choline oxidation pathway for methylation in vivo;Burns;Biochim Biophys Acta,1998

5. 1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolism;Wevers;Clin Chem,1999

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