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Diagnosis of inborn errors of metabolism using 1H NMR spectroscopic analysis of urine

  • Published:1999-05 Issue:3 Volume:22 Page:297-301
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Bamforth F. J.1,Dorian V.2,Vallance H.3,Wishart D. S.4

Affiliation:

1. ; Department of Laboratory Medicine and Pathology; University of Alberta; Edmonton Alberta Canada

2. BioTools Incorporated; Edmonton Alberta Canada

3. ; BC Children's Hospital; Vancouver British Columbia Canada

4. ; Faculty of Pharmacy and Pharmaceutical Sciences; University of Alberta; Edmonton Alberta Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. Automatic data reduction and pattern recognition methods for analysis of 1H nuclear magnetic resonance spectra of human urine from normal and pathological states;Holmes;Anal Biochem,1994

2. In vitro NMR spectroscopy in the diagnosis and investigation of metabolic disorders;Iles;Q Magn Res Biol Med,1995

3. An introduction to the potential of 1H-, 31P-and 13-NMR-spectroscopy;Leibfritz;Anticancer Res,1996

4. Parallel Distributed Processing
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