Literature DB >> 1749220

Techniques for studying hepatic metabolism in vivo.

J V Leonard1, G N Thompson.   

Abstract

Techniques for studying metabolic events in vivo in patients with inborn errors are reviewed. Loading or provocation tests that have been used widely are insensitive and frequently non-specific. Compounds labelled with stable isotopes can be used to study enzyme kinetics and substrate turnover, providing more detailed and specific information. Intracellular events may be studied using nuclear magnetic resonance spectroscopy. The results using these techniques to study patients with selected inborn errors are discussed, namely phenylketonuria, glycogen storage disease type I and propionic acidaemia.

Entities:  

Mesh:

Year:  1991        PMID: 1749220     DOI: 10.1007/bf01797925

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  17 in total

1.  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

2.  Glucose production rates in type 1 glycogen storage disease.

Authors:  J E Collins; K Bartlett; J V Leonard; A Aynsley-Green
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses.

Authors:  J Fernandes; J F Koster; W F Grose; N Sorgedrager
Journal:  Arch Dis Child       Date:  1974-03       Impact factor: 3.791

4.  Value of the glucagon test in screening for hepatic glycogen storage disease.

Authors:  D B Dunger; J V Leonard
Journal:  Arch Dis Child       Date:  1982-05       Impact factor: 3.791

5.  Intravenous galactose tolerance test with the use of an enzymatic method for the determination of galactose.

Authors:  B Tengström; M Hjelm; C H de Verdier; I Werner
Journal:  Am J Dig Dis       Date:  1967-09

6.  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

7.  The fasting test in paediatrics: application to the diagnosis of pathological hypo- and hyperketotic states.

Authors:  J P Bonnefont; N B Specola; A Vassault; A Lombes; H Ogier; J B de Klerk; A Munnich; M Coude; M Paturneau-Jouas; J M Saudubray
Journal:  Eur J Pediatr       Date:  1990-12       Impact factor: 3.183

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.  Natural-abundance 13C NMR study of glycogen repletion in human liver and muscle.

Authors:  T Jue; D L Rothman; B A Tavitian; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.