G. Thompson

发表

Failure of taurine to improve fat absorption in cystic fibrosis

G. Thompson, 1988, Journal of Inherited Metabolic Disease.

Relationships between essential fatty acid levels, pulmonary function and fat absorption in pre-adolescent cystic fibrosis children with good clinical scores

G. Thompson, 2004, European Journal of Pediatrics.

Taurine supplementation, fat absorption, and growth in cystic fibrosis.

G. Davidson, G. Thompson, T. Robb, 1987, The Journal of pediatrics.

Determinants of Serum Vitamin D Levels in Preadolescent Cystic Fibrosis Children

G. Thompson, G. Thompson, 1987, Acta paediatrica Scandinavica.

A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion

H. Dahl, D. Thorburn, G. Thompson, 2004, Human Genetics.

Sources of propionate in inborn errors of propionate metabolism.

S. Lyonnet, J. Leonard, J. Saudubray, 1990, Metabolism: clinical and experimental.

Practical considerations in the use of stable isotope labelled compounds as tracers in clinical studies.

D. Halliday, G. Thompson, G. C. Ford, 1989, Biomedical & environmental mass spectrometry.

Stable isotopes as tracers in clinical research.

G. Thompson, D. Halliday, K. Cheng, 1989, Annals of nutrition & metabolism.

Protein and leucine metabolism in maple syrup urine disease.

J. Leonard, J. Saudubray, J. Bresson, 1990, The American journal of physiology.

Increased Urinary Metabolite Excretion during Fasting in Disorders of Propionate Metabolism

R. Chalmers, G. Thompson, 1990, Pediatric Research.

Relationships between plasma isotope enrichments of leucine and α‐ketoisocaproic acid during continuous infusion of labelled leucine

D. Halliday, G. Thompson, G. C. Ford, 1988, European journal of clinical investigation.

Rapid measurement of whole body and forearm protein turnover using a [2H5]phenylalanine model.

D. Halliday, G. Thompson, G. C. Ford, 1989, The American journal of physiology.

In vivo enzyme activity in inborn errors of metabolism.

J. Leonard, J. Walter, G. Thompson, 1990, Metabolism: clinical and experimental.

Parenteral nutrition in propionic acidemia and methylmalonic acidemia.

J. Leonard, J. Walter, G. Thompson, 1990, The Journal of pediatrics.

Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemia.

J. Leonard, J. Saudubray, J. Bresson, 1989, The Journal of pediatrics.

Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionate.

C. Heatherington, J. Leonard, J. Walter, 1989, Clinica chimica acta; international journal of clinical chemistry.

CONTRIBUTION OF AMINOACID CATABOLISM TO PROPIONATE PRODUCTION IN METHYLMALONIC ACIDAEMIA

J. Leonard, J. Walter, K. Bartlett, 1989, The Lancet.

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

J. Leonard, J. Saudubray, J. Bresson, 1990, European Journal of Pediatrics.

Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency

S. Rahman, J. Leonard, S. Heales, 1994, Journal of Inherited Metabolic Disease.

Maternal tyrosinaemia II: Management and successful outcome

D. Francis, G. Thompson, D. Kirby, 1992, European Journal of Pediatrics.

In vivo disposal of phenylalanine in phenylketonuria: A study of two siblings

R. Cotton, J. Pitt, S. Ramus, 1996, Journal of Inherited Metabolic Disease.

Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients

C. Stanley, Shupei Wang, M. Robert, 2001, Pediatric Research.

Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.

G. Thompson, D. Halliday, 1990, The Journal of clinical investigation.

The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria

R. Chalmers, G. Thompson, D. Halliday, 1990, European Journal of Pediatrics.

Protein metabolism in cystic fibrosis: responses to malnutrition and taurine supplementation.

F. Tomas, G. Thompson, 1987, The American journal of clinical nutrition.

Techniques for studying hepatic metabolismin vivo

J. Leonard, G. Thompson, 1991, Journal of Inherited Metabolic Disease.

Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase.

C. Stanley, B. Y. Hsu, J. Pitt, 1997, The New England journal of medicine.

Protein turnover in pregnancy.

G. Thompson, D. Halliday, 1992, European journal of clinical nutrition.

Assessment of taurine deficiency in cystic fibrosis.

G. Thompson, 1988, Clinica chimica acta; international journal of clinical chemistry.

Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.

C. Obie, D. Valle, K. Schappert, 1995, American journal of human genetics.

Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolism.

D. Howells, F. Shann, W. Butt, 1991, The Journal of pediatrics.

Acute illness in maple syrup urine disease: dynamics of protein metabolism and implications for management.

D. Francis, G. Thompson, D. Halliday, 1991, The Journal of pediatrics.

GUT BACTERIAL METABOLISM

J. Walter, K. Bartlett, G. Thompson, 1988, The Lancet.

A fluorimetric assay for succinic semialdehyde dehydrogenase activity suitable for prenatal diagnosis of the enzyme deficiency

D. Howells, D. Thorburn, G. Thompson, 1993, Journal of Inherited Metabolic Disease.

Stable isotope dilution analysis of GABA in CSF using simple solvent extraction and electron-capture negative-ion mass fragmentography

D. Howells, C. Jakobs, G. Thompson, 1993, Journal of Inherited Metabolic Disease.

The use of metronidazole in management of methylmalonic and propionic acidaemias

S. Lyonnet, J. Leonard, J. Saudubray, 1990, European Journal of Pediatrics.

In Vivo Bile Acid Uptake from Terminal Ileum in Cystic Fibrosis

G. Davidson, G. Thompson, 1988, Pediatric Research.

Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentration.

D. Francis, G. Thompson, D. Kirby, 1991, Archives of disease in childhood.

Protein Metabolism in Phenylketonuria and Lesch-Nyhan Syndrome

R. Watts, G. Thompson, D. Halliday, 1990, Pediatric Research.

Type V hyperlipoproteinaemia in neonates.

J. Bresson, I. H. Craig, G. Thompson, 1987, Archives of Disease in Childhood.

Taurine uptake by normal and cystic fibrosis fibroblasts.

G. Thompson, 1988, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolism.

A. Mariotti, J. Saudubray, G. Thompson, 1994, The American journal of clinical nutrition.

PROPIONATE PRODUCTION IN METHYLMALONIC ACIDAEMIA

J. Leonard, J. Walter, G. Thompson, 1989, The Lancet.