Localized Proton MR Spectroscopy in Infants with Urea Cycle Defect

References

1. ↵
   Brusilow SW. In born error of urea synthesis: paradigm of hyperammonemic encephalopathy. In: Berg BO, eds. Principles of Child Neurology. St. Louis: McGraw-Hill; 1996:979–995
2. ↵
   Klose U. In vivo proton spectroscopy in presence of eddy currents. Magn Reson Med 1990;14:26-30

   PubMedWeb of Science
3. ↵
   Michaelis T, Merboldt KD, Haenicke W, Gyngell ML, Bruhn H, Frahm J. On the identification of cerebral metabolites in localized ¹H NMR spectra of human brain in vivo. NMR Biomed 1991;4:90-98

   PubMedWeb of Science
4. ↵
   Meijer AJ, Lamers WH, Chamuleau AFM. Nitrogen metabolism and ornithine cycle function. Physiol Rev 1990;70:701-748

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5. ↵
   Bosman DK, Deutz NEF, De Graaf AA, et al. Changes in brain metabolism during hyperammonemia and acute liver failure: results of a comparative 1H-NMR spectroscopy and biochemical investigation. Hepatology 1990;12:281-290

   PubMedWeb of Science
6. ↵
   Connelly A, Cross JH, Gardian DG, Hunter JV, Kirkham IJ, Leonard JV. Magnetic resonance spectroscopy shows increased brain glutamine in ornithine carbamoyl transferase deficiency. Pediatr Res 1993;33:77-81

   PubMedWeb of Science
7. ↵
   Hawkins RA, Jessy J, Mans AM, De Joseph MR. Effect of reducing brain glutamine synthesis on metabolic symptoms of hepatic encephalopathy. J Neurochem 1993;60:1000-1006

   CrossRefPubMedWeb of Science
8. ↵
   Kreis R, Ross BD, Farrow NA, Ackerman Z. Metabolic disorders of the brain in chronic hepatic encephalopathy detected with H-1 MR spectroscopy. Radiology 1992;182:19-27

   PubMedWeb of Science
9. ↵
   Ernst T, Ross BD, Flores R. Cerebral MRS in infant with suspected Reye's syndrome. Lancet 1992;340:486
10. Ross BD, Blüml S. New aspects of brain physiology. NMR Biomed 1996;9:279-296

    CrossRefPubMedWeb of Science