Application of nuclear magnetic resonance spectroscopy combined with principal component analysis in detecting inborn errors of metabolism using blood spots: a metabonomic approach
- 1 May 2004
- journal article
- Published by Elsevier in Analytica Chimica Acta
- Vol. 511 (2) , 303-312
- https://doi.org/10.1016/j.aca.2004.02.012
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Pattern recognition methods and applications in biomedical magnetic resonanceProgress in Nuclear Magnetic Resonance Spectroscopy, 2001
- An NMR‐based metabonomic approach to investigate the biochemical consequences of genetic strain differences: application to the C57BL10J and Alpk:ApfCD mouseFEBS Letters, 2000
- Survey of scope of neonatal screening in the United KingdomBMJ, 1995
- 750 MHz 1H and 1H-13C NMR Spectroscopy of Human Blood PlasmaAnalytical Chemistry, 1995
- A new approach to the newborn screening for hyperphenylalaninemias: use of L-phenylalanine dehydrogenase and microtiter platesClinica Chimica Acta; International Journal of Clinical Chemistry, 1990
- Isocratic reverse-phase liquid chromatography assay for amino acid metabolic disorders using eluates of dried blood spotsAnalytical Biochemistry, 1990
- 1H NMR studies of urine from premature and sick babiesMagnetic Resonance in Medicine, 1989
- High resolution proton magnetic resonance spectroscopy of biological fluidsProgress in Nuclear Magnetic Resonance Spectroscopy, 1989
- Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometryEuropean Journal of Pediatrics, 1986
- Molecular aspects of genetic heterogeneityPublished by Springer Nature ,1982