Literature DB >> 7957391

The investigation of inborn errors in vivo using stable isotopes.

J V Leonard1, S J Heales.   

Abstract

By labelling compounds with stable isotopes metabolic events can be studied in vivo. Pathways can be investigated and both enzyme and substrate kinetics measured. The concept of labelling substrates to investigate metabolic events in vivo is straightforward but there are potential sources of error that must be recognised. Patients with a wide range of inborn errors have now been studied. In some there is negligible residual enzyme activity but in others, even those with no activity in vitro, residual enzyme activity is apparently present in vivo, probably as a result of metabolic activity of alternative pathways. These studies have demonstrated the importance of such pathways and have provided insight into the biochemical adaptations that occur in patients with inherited metabolic disorders.

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Year:  1994        PMID: 7957391     DOI: 10.1007/BF02138782

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  10 in total

1.  The use of metronidazole in management of methylmalonic and propionic acidaemias.

Authors:  G N Thompson; R A Chalmers; J H Walter; J L Bresson; S L Lyonnet; P J Reed; J M Saudubray; J V Leonard; D Halliday
Journal:  Eur J Pediatr       Date:  1990-08       Impact factor: 3.183

2.  A simple isotopic technique for assessing vitamin responsiveness in vivo in propionic acidaemia.

Authors:  G N Thompson; J L Bresson; J P Bonnefont; J H Walter; M A Read; J M Saudubray; J V Leonard; D Halliday
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemia.

Authors:  J H Walter; G N Thompson; J V Leonard; K Bartlett; D Halliday
Journal:  Lancet       Date:  1989-06-10       Impact factor: 79.321

Review 4.  Tracers in metabolic research: radioisotope and stable isotope/mass spectrometry methods.

Authors:  R R Wolfe
Journal:  Lab Res Methods Biol Med       Date:  1984

5.  Tolerance of phenylalanine after ntravenous administration in phenylketonurics, heterozygous carriers, and normal adults.

Authors:  H J Bremer; W Neumann
Journal:  Nature       Date:  1966-03-12       Impact factor: 49.962

6.  Protein and leucine metabolism in maple syrup urine disease.

Authors:  G N Thompson; J L Bresson; P J Pacy; J P Bonnefont; J H Walter; J V Leonard; J M Saudubray; D Halliday
Journal:  Am J Physiol       Date:  1990-04

7.  Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.

Authors:  G N Thompson; D Halliday
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

8.  Detection of heterozygous carriers for phenylketonuria by a L-[2H5]phenylalanine stable isotope loading test.

Authors:  W D Lehmann; N Theobald; H C Heinrich; P Clemens; R Grüttner
Journal:  Clin Chim Acta       Date:  1984-03-27       Impact factor: 3.786

9.  In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolism.

Authors:  G N Thompson; J H Walter; J L Bresson; J P Bonnefont; J M Saudubray; J V Leonard; D Halliday
Journal:  Eur J Pediatr       Date:  1990-03       Impact factor: 3.183

10.  The conversion of phenylalanine to tyrosine in man. Direct measurement by continuous intravenous tracer infusions of L-[ring-2H5]phenylalanine and L-[1-13C] tyrosine in the postabsorptive state.

Authors:  J T Clarke; D M Bier
Journal:  Metabolism       Date:  1982-10       Impact factor: 8.694

  10 in total
  1 in total

Review 1.  The management and outcome of propionic and methylmalonic acidaemia.

Authors:  J V Leonard
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

  1 in total

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