K. Bartlett

发表

S. Eaton, K. Bartlett, 2004, European journal of biochemistry.

Combined enzyme defect of mitochondrial fatty acid oxidation.

D. Turnbull, L. Bindoff, M. Pourfarzam, 1992, The Journal of clinical investigation.

Tandem mass spectrometry — The potential

M. Pourfarzam, K. Bartlett, 1999, Journal of Inherited Metabolic Disease.

The measurement of carnitine and acyl-carnitines: application to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidation.

D. Turnbull, J. Leonard, A. Aynsley-Green, 1992, Clinica chimica acta; international journal of clinical chemistry.

Acyl‐CoA Dehydrogenases

K. Bartlett, 2002 .

Mammalian mitochondrial beta-oxidation.

S. Eaton, M. Pourfarzam, K. Bartlett, 1996, The Biochemical journal.

Effects of feeding on albumin synthesis in hypoalbuminemic hemodialysis patients.

J. Louden, T. Goodship, K. Bartlett, 2002, Kidney international.

Inherited Disorders of Vitamins and Cofactors

G. Addison, R. Harkness, K. Bartlett, 1985, Springer Netherlands.

Whole body protein metabolism in children with cancer.

A. Craft, D. Halliday, S. Daley, 1996, Archives of disease in childhood.

Defects of fatty acid oxidation in skeletal muscle

I. M. Shepherd, D. Turnbull, N. Watmough, 1987, Journal of Inherited Metabolic Disease.

Tissue Specific Differences in Intramitochondrial Control of β-Oxidation

S. Eaton, K. Bartlett, 2002 .

Very long‐chain acyl coenzyme A dehydrogenase deficiency presenting with exercise‐induced myoglobinuria

D. Turnbull, M. Pourfarzam, S. Jackson, 1994, Neurology.

Analysisof FattyAcidOxidationIntermediates in CulturedFibroblasts to Detect Mitochondrial OxidationDisorders

D. Turnbull, M. Pourfarzam, J. Schaefer, 1994 .

Analysis of fatty acid oxidation intermediates in cultured fibroblasts to detect mitochondrial oxidation disorders.

D. Turnbull, M. Pourfarzam, D. Turnbull, 1994, Clinical chemistry.

Skeletal muscle mitochondrial β-oxidation of dicarboxylates

M. Pourfarzam, K. Bartlett, 1993 .

Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy

D. Turnbull, M. Johnson, J. Eyre, 1988, Developmental medicine and child neurology.

The effect of high glucose on polyol pathway activity and myoinositol metabolism in cultured human endothelial cells

K. Alberti, C. Hetherington, K. Bartlett, 1989, Diabetologia.

Sodium bicarbonate treatment and ubiquitin gene expression in acidotic human subjects with chronic renal failure

T. Goodship, K. Bartlett, C. Redfern, 2002, European journal of clinical investigation.

Fatal Lactic Acidosis in Infancy with a Defect of Complex III of the Respiratory Chain

I. M. Shepherd, D. Turnbull, V. Darley-Usmar, 1989, Pediatric Research.

Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.

D. Turnbull, C. Ragan, L. Bindoff, 1990, The Journal of clinical investigation.

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

L. D. Schroeder, E. R. Baumgartner, L. Bolund, 1999, American journal of human genetics.

Intramitochondrial control of the oxidation of hexadecanoate in skeletal muscle. A study of the acyl-CoA esters which accumulate during rat skeletal-muscle mitochondrial beta-oxidation of [U-14C]hexadecanoate and [U-14C]hexadecanoyl-carnitine.

D. Turnbull, S. Eaton, K. Bartlett, 1993, The Biochemical journal.

Intermediates of myocardial mitochondrial beta-oxidation: possible channelling of NADH and of CoA esters.

S. Eaton, M. Pourfarzam, K. Bartlett, 1999, Biochimica et biophysica acta.

The role of pancreatic insulin secretion in neonatal glucoregulation. II. Infants with disordered blood glucose homoeostasis.

J. Hawdon, A. Aynsley-Green, M. W. Ward Platt, 1993, Archives of disease in childhood.

Carnitine palmitoyl transferase I and the control of myocardial beta-oxidation flux.

S. Eaton, K. Fukumoto, A. Pierro, 2001, Biochemical Society transactions.

A role for coenzyme Q in alcoholic liver disease

S. Eaton, K. Bartlett, C. Record, 2000 .

Mitochondrial b-oxidation

S. Eaton, K. Bartlett, 2004 .

Carnitine palmitoyl transferase I and malonyl-CoA in the heart and skeletal muscle : does control analysis help to explain the paradox ?

S. Eaton, K. Bartlett, P. Quant, 2000 .

Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency.

D. Turnbull, K. Alberti, M. Johnson, 1984, The New England journal of medicine.

Whole body leucine turnover and nutritional status in continuous ambulatory peritoneal dialysis.

R. Wilkinson, T. Goodship, M. Ward, 1987, Clinical science.

Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness

R. Pollitt, K. Bartlett, M. Tanner, 1989, Journal of Inherited Metabolic Disease.

Growth and body composition of dairy calves fed milk replacers containing different amounts of protein at two feeding rates.

J. Drackley, F. Mckeith, M. VandeHaar, 2006, Journal of animal science.

Mammalian mitochondrial β-oxidation

S. Eaton, M. Pourfarzam, K. Bartlett, 1996 .

Effect of oral antibiotics on intestinal production of propionic acid

J. Mathers, K. Bartlett, A. Mellon, 2000, Archives of disease in childhood.

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.

Changes in protein turnover, IGF‐I and IGF binding proteins in children with cancer

D. Halliday, S. Daley, A. Cotterill, 1998, Acta paediatrica.

Plasma coenzyme Q(10) in children and adolescents undergoing doxorubicin therapy.

S. Eaton, M. Pourfarzam, R. Skinner, 2000, Clinica chimica acta; international journal of clinical chemistry.

Synaptosomal glutamate transport in thioacetamide‐induced hepatic encephalopathy in the rat

C. Record, K. Bartlett, K. Oppong, 1995, Hepatology.

The application of fluorometric fast centrifugal analysis to the detection of biotinidase deficiency

K. Bartlett, A. Skillen, A. Shein, 1987, Journal of Inherited Metabolic Disease.

Enzyme studies in biotin-responsive disorders

K. Bartlett, H. Ghneim, H. Wastell, 1985, Journal of Inherited Metabolic Disease.

A new solid-phase assay for biotin and biocytin and its application to the study of patients with biotinidase deficiency.

P. W. Chan, K. Bartlett, K. Bartlett, 1986, Clinica chimica acta; international journal of clinical chemistry.

COMBINED CARBOXYLASE DEFECT: BIOTIN-RESPONSIVENESS IN CULTURED FIBROBLASTS

D. Gompertz, K. Bartlett, 1976, The Lancet.

Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.

D. Gompertz, D. Blair, K. Bartlett, 1973, Archives of disease in childhood.

Metabolic consequences of methylenecyclopropylglycine poisoning in rats.

S. Ghisla, S. Jackson, K. Bartlett, 1991, The Biochemical journal.

Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.

D. Turnbull, M. Birch-Machin, K. Bartlett, 1993, Biochimica et biophysica acta.

Intermediates of peroxisomal β‐oxidation of [U‐14C]hexadecanedionoate

M. Pourfarzam, K. Bartlett, 1992 .

Measurement of the acyl-CoA intermediates of beta-oxidation by h.p.l.c. with on-line radiochemical and photodiode-array detection. Application to the study of [U-14C]hexadecanoate oxidation by intact rat liver mitochondria.

D. Turnbull, N. Watmough, K. Bartlett, 1989, The Biochemical journal.

INBORN ERRORS OF METABOLISM AND UNEXPECTED INFANT DEATHS

J. Leonard, A. Green, K. Bartlett, 1988, The Lancet.

Glucose production rates in type 1 glycogen storage disease

J. Leonard, A. Aynsley-Green, K. Bartlett, 1990, Journal of Inherited Metabolic Disease.

[11] Radiochemical high-performance liquid chromatography methods for the study of branched-chain amino acid metabolism

K. Bartlett, A. G. Causey, 1988 .

Vitamin-responsive inborn errors of metabolism.

K. Bartlett, 1983, Advances in clinical chemistry.

Effects of ciprofibrate and 2-[5-(4-chlorophenyl)pentyl]oxirane-2-carboxylate (POCA) on the distribution of carnitine and CoA and their acyl-esters and on enzyme activities in rats. Relation between hepatic carnitine concentration and carnitine acetyltransferase activity.

L. Agius, K. Bartlett, A. Bhuiyan, 1988, The Biochemical journal.

The effects of 2[5(4-chlorophenyl)pentyl]oxirane-2-carbonyl-Co-A on mitochondrial oxidations.

D. Turnbull, K. Bartlett, H. Sherratt, 1984, Biochemical pharmacology.

Multiple biochemical effects in the pathogenesis of alcoholic fatty liver

S. Eaton, K. Bartlett, C. Record, 1997, European journal of clinical investigation.

Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia

J. Leonard, M. Pourfarzam, A. Aynsley-Green, 1995, Journal of Inherited Metabolic Disease.

Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.

D. Turnbull, L. Bindoff, S. Eaton, 1991, The Journal of biological chemistry.

New developments in neonatal screening

S. Eaton, M. Pourfarzam, K. Bartlett, 1997, Archives of disease in childhood. Fetal and neonatal edition.

Fatty Acid Oxidation in Peripheral Blood Cells: Characterization and Use for the Diagnosis of Defects of Fatty Acid Oxidation

D. Turnbull, M. Pourfarzam, S. Jackson, 1995, Pediatric Research.

Blood and brain concentrations of mercaptans in hepatic and methanethiol induced coma.

C. Record, K. Bartlett, C. Record, 1984, Gut.

BIOTINIDASE DEFICIENCY AND THE EYE AND EAR

L. Taitz, A. Green, K. Bartlett, 1983, The Lancet.

A sensitive fluorimetric rate assay for biotinidase using a new derivative of biotin, biotinyl-6-aminoquinoline.

K. Bartlett, H. Wastell, G. Dale, 1984, Analytical biochemistry.

Control of Mitochondrial β-Oxidation at the Levels of [NAD+]/[NADH] and CoA Acylation

S. Eaton, M. Pourfarzam, B. Middleton, 2002 .

Non-glucose metabolism in cancer cells—is it all in the fat?

J. Lunec, S. Biswas, K. Bartlett, 2012, Cancer and Metastasis Reviews.

A new method for the detection of hydrogen in breath and its application to acquired and inborn sugar malabsorption.

J. V. Dobson, K. Bartlett, E. Eastham, 1980, Clinica chimica acta; international journal of clinical chemistry.

Altered acyl-CoA metabolism in riboflavin deficiency.

J. Vamecq, F. Van hoof, K. Bartlett, 1989, Biochimica et biophysica acta.

Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.

D. Turnbull, L. Bindoff, M. Pourfarzam, 1992, Progress in clinical and biological research.

Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs

M. Durán, D. Ketting, S. K. Wadman, 1982, European Journal of Pediatrics.

Organic aciduria in rats made resistant to hypoglycin toxicity by pretreatment with clofibrate.

K. Bartlett, H. Sherratt, R. Veitch, 1987, Biochemical Journal.

Pyruvate carboxylase deficiency

K. Alberti, K. Bartlett, H. Ghneim, 1984, Journal of Inherited Metabolic Disease.

The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe.

B. Robinson, J. Saudubray, J. Oei, 1987, American journal of human genetics.

Enzyme Studies in Combined Carboxylase Deficiency

J. Leonard, K. Bartlett, H. Ghneim, 1985, Annals of the New York Academy of Sciences.

Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation

J. Leonard, A. Green, A. Green, 1981, Journal of Inherited Metabolic Disease.

Biotin‐reversible neurodegenerative disease in infancy

L. Low, K. Bartlett, J. Seakins, 1986, Australian paediatric journal.

The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemias.

D. Gompertz, K. Bartlett, 1974, Biochemical medicine.

Evidence for the enzymic defect in β‐methylcrotonylglycinuria

D. Gompertz, K. Bartlett, P. Goodey, 1973 .

MECHANISM OF BIOTIN-RESPONSIVE COMBINED CARBOXYLASE DEFICIENCY

K. Bartlett, H. Ghneim, 1982, The Lancet.

3-Ketothiolase deficiency

R. A. Cannon, W. Nyhan, B. Middleton, 1986, European Journal of Pediatrics.

A defect in l-isoleucine metabolism associated with α-methyl-β-hydroxybutyric and α-methylacetoacetic aciduria: Quantitative in vivo and in vitro studies

J. Saudubray, G. Draffan, D. Gompertz, 1974 .

Inherited disorders of 3-methylcrotonyl CoA carboxylation.

J. Leonard, K. Bartlett, J. Seakins, 1981, Archives of disease in childhood.

A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.

J. Leonard, K. Bartlett, H. Ng, 1980, Clinica chimica acta; international journal of clinical chemistry.

Biotin activation of carboxylase activity in cultured fibroblasts from a child with a combined carboxylase defect.

D. Gompertz, K. Bartlett, 1978, Clinica chimica acta; international journal of clinical chemistry.

Biotinidase deficiency: a survey of 10 cases.

K. Bartlett, H. Wastell, A. Shein, 1988, Archives of disease in childhood.

Long-term auditory and visual complications of biotinidase deficiency.

L. Taitz, J. Leonard, K. Bartlett, 1985, Early human development.

Defects of β-oxidation including carnitine deficiency

M. Pourfarzam, K. Bartlett, 2002 .

Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

D. Turnbull, J. Leonard, S. Jackson, 1991, Pediatric Research.

3‐Hydroxyacyl‐CoA Dehydrogenases

K. Bartlett, 2002 .

Methods for the investigation of hypoglycaemia with particular reference to inherited disorders of mitochondrial beta-oxidation.

K. Bartlett, 1993, Bailliere's clinical endocrinology and metabolism.

Inherited disorders of mitochondrial fatty acid oxidation

M. Pourfarzam, K. Bartlett, 1997 .

Isolated biotin-resistant 3-methylcrotonyl CoA carboxylase deficiency presenting with life-threatening hypoglycaemia

M. Bennett, R. Pollitt, H. Worth, 1984, Journal of Inherited Metabolic Disease.

GUT BACTERIAL METABOLISM

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

β-Ketothiolase deficiency with favourable evolution

O. Giardini, C. Bachmann, M. Castro, 1987, Journal of Inherited Metabolic Disease.

Effects of added l-carnitine, acetyl-CoA and CoA on peroxisomal beta-oxidation of [U-14C]hexadecanoate by isolated peroxisomal fractions.

M. Pourfarzam, H. Osmundsen, K. Bartlett, 1995, Biochimica et biophysica acta.

Metabolism of acetyl-CoA by isolated peroxisomal fractions: formation of acetate and acetoacetyl-CoA.

H. Osmundsen, K. Bartlett, R. Hovik, 1991, Journal of lipid research.

HEPATIC PEROXISOMAL PROLIFERATION CAUSED BY ETHYL 2[5(4‐CHLORO‐PHENYL)PENTYL]OXIRAN‐2‐ CARBOXYLATE (CPOC): A HYPOGLYCEMIC INHIBITOR OF MITOCHONDRIAL FATTY ACID OXIDATION

D. Turnbull, H. Osmundsen, F. Hoof, 1982 .

Synthesis, purification, and characterization of dicarboxylylmono-coenzyme A esters.

M. Pourfarzam, K. Bartlett, 1997, Methods in enzymology.

Synthesis, characterisation and high-performance liquid chromatography of C6-C16 dicarboxylyl-mono-coenzyme A and -mono-carnitine esters.

M. Pourfarzam, K. Bartlett, 1991, Journal of chromatography.

A radio-HPLC assay for the measurement of methylmalonyl-CoA mutase.

K. Bartlett, A. G. Causey, 1984, Clinica chimica acta; international journal of clinical chemistry.

The effects of large doses of biotin on leucocyte carboxylases in humans

K. Alberti, K. Bartlett, J. Stirk, 1983 .

The relationship between plasma biotin concentration and circulating leucocyte beta-methylcrotonyl-CoA carboxylase and propionyl-CoA carboxylase.

D. Gompertz, K. Bartlett, T. Horsburgh, 1980, Clinical science.

Sterol esters of Phycomyces blakesleeanus

E. Mercer, K. Bartlett, 1974 .

Redox control of beta-oxidation in rat liver mitochondria.

D. Turnbull, S. Eaton, K. Bartlett, 1994, European journal of biochemistry.

Redox control of P-oxidation in rat liver mitochondria

D. Turnbull, S. Eaton, K. Bartlett, 1994 .

Effect of methionine loading and endogenous hypermethioninaemia on blood mercaptans in man.

J. Leonard, K. Bartlett, C. Record, 1988, Clinica chimica acta; international journal of clinical chemistry.

Comparative value of different dialysis membranes, including a carbon coated membrane for removal of noxious substances in hepatic coma.

N. Hoenich, K. Bartlett, C. Record, 1979, The International journal of artificial organs.

Misfolding, Degradation, and Aggregation of Variant Proteins

L. Bolund, P. Bross, J. Vockley, 2003, Journal of Biological Chemistry.

The mitochondrial trifunctional protein: centre of a beta-oxidation metabolon?

S. Eaton, M. Pourfarzam, B. Middleton, 2000, Biochemical Society transactions.

Methodological Approaches in Studies of Altered Mitochondrial and Peroxisomal β-Oxidation

H. Osmundsen, K. Bartlett, H. Sherratt, 1987 .

Control of mitochondrial beta-oxidation: sensitivity of the trifunctional protein to [NAD+]/[NADH] and [acetyl-CoA]/[CoA].

S. Eaton, B. Middleton, K. Bartlett, 1998, Biochimica et biophysica acta.

Short-term studies on the use of amino acids as an osmotic agent in continuous ambulatory peritoneal dialysis.

R. Wilkinson, T. Goodship, M. Ward, 1987, Clinical science.

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.

R M Winter, R. Winter, J. Burn, 1998, Journal of medical genetics.

Short-chain acyl-CoA dehydrogenase deficiency.

I. M. Shepherd, D. Turnbull, K. Bartlett, 1990, Progress in clinical and biological research.

Liver and biliary Impaired acetaldehyde metabolism in patients with non-alcoholic liver disorders

K. Bartlett, K. Matthewson, C. Record, 2006 .

Intermediates of peroxisomal β-oxidation. A study of the fatty acyl-CoA esters which accumulate during peroxisomal β-oxidation of [U-14C]hexadecanoate

S. Eaton, H. Osmundsen, N. Watmough, 1990 .

A study of the metabolism of [U-14C]3-methyl-2-oxopentanoate by rat liver mitochondria using h.p.l.c. with continuous on-line monitoring of radioactive intact acyl-coenzyme A intermediates.

B. Middleton, K. Bartlett, A. G. Causey, 1986, The Biochemical journal.

The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria.

B. Middleton, K. Bartlett, 1983, Clinica chimica acta; international journal of clinical chemistry.

The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria. Implications for our understanding of mitochondrial cytopathies in man.

D. Turnbull, M. Birch-Machin, K. Bartlett, 1994, The Journal of biological chemistry.

The management and long term outcome of organic acidaemias

J. Leonard, E. Naughten, K. Bartlett, 1984, Journal of Inherited Metabolic Disease.

Skeletal muscle mitochondrial beta-oxidation. A study of the products of oxidation of [U-14C]hexadecanoate by h.p.l.c. using continuous on-line radiochemical detection.

D. Turnbull, N. Watmough, K. Bartlett, 1988, The Biochemical journal.

Products and intermediates of the beta-oxidation of [U-14C]hexadecanedionoyl-mono-CoA by rat liver peroxisomes and mitochondria.

M. Pourfarzam, K. Bartlett, 1991, The Biochemical journal.

Production and export of acylcarnitine esters by neonatal rat hepatocytes.

S. Eaton, M. Pourfarzam, M. Markley, 1999, Advances in experimental medicine and biology.

Human forearm arteriovenous differences of carnitine, short-chain acylcarnitine and long-chain acylcarnitine.

K. Alberti, P. Butler, A. Aynsley-Green, 1989, Clinical science.

Skeletal muscle mitochondrial beta-oxidation of dicarboxylates.

M. Pourfarzam, K. Bartlett, 1993, Biochimica et biophysica acta.

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets

D. Turnbull, M. Pourfarzam, S. Jackson, 1992, Journal of Inherited Metabolic Disease.

Exploratory Data Analysis for Investigating GC-MS Biomarkers

Kenneth McGarry, Kim Bartlett, Morteza Pourfarzam, 2008, PRIB.

Supplementation of 1% L-glutamine to milk replacer does not overcome the growth depression in calves caused by soy protein concentrate.

K. Bailey, J. Drackley, K. Bartlett, 2006, Journal of dairy science.

Identification of urinary metabolites of sodium dipropylacetate in man; potential sources of interference in organic acid screening procedures.

T. Baillie, D. Gompertz, K. Bartlett, 1977, Clinica chimica acta; international journal of clinical chemistry.

An improved gas chromatographic method for the detection and quantitation of mercaptans in blood.

K. Bartlett, C. Record, H. Mardini, 1981, Clinica chimica acta; international journal of clinical chemistry.

Reverse-phase high-performance liquid chromatographic analysis of short-, medium- and long-chain acylcarnitines in urine and plasma

K. Bartlett, A. Bhuiyan, 1988 .

A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiency.

D. Turnbull, J. Leonard, A. Aynsley-Green, 1987, Clinica chimica acta; international journal of clinical chemistry.

Variation in the levels and composition of the sterols and sterol esters of Phycomyces blakesleeanus with age of culture

E. Mercer, K. Bartlett, 1974 .

Kinetics of enzymes requiring long-chain acyl-CoA esters as substrates: effects of substrate binding to albumin.

P. Bartlett, N. Bartlett, K. Bartlett, 1985, The Biochemical journal.

[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)].

J. Saudubray, F. Coudé, D. Gompertz, 1980, Archives francaises de pediatrie.

The effects of valproate on intermediary metabolism in isolated rat hepatocytes and intact rats.

D. Turnbull, K. Bartlett, A. Bone, 1983, Biochemical pharmacology.

Inhibition of mitochondrial β-oxidation at the stage of carnitine palmitoyltransferase I by the coenzyme A esters of some substituted hypoglycaemic oxiran-2-carboxylic acids

D. Turnbull, K. Bartlett, A. Bone, 1981 .

An HPLC assay for sn-1,2-diacylglycerol.

S. Eaton, K. Bartlett, H. Al-Mardini, 1995, Clinica chimica acta; international journal of clinical chemistry.

Carnitine palmitoyl transferase I and the control of beta-oxidation in heart mitochondria.

S. Eaton, K. Bartlett, P. Quant, 2001, Biochemical and biophysical research communications.

Lipid storage myopathy associated with low acyl-CoA dehydrogenase activities.

D. Turnbull, M. Johnson, B. Ashworth, 1988, Brain : a journal of neurology.

The effects of some short-chain fatty acids on pyruvate carboxylase activity in intact isolated rat liver mitochondria

K. Bartlett, H. Sherratt, J. Stirk, 1983 .

Thermal desorption-gas chromatography of plasma isovaleraldehyde in hepatic encephalopathy in man.

R. Williams, K. Bartlett, C. J. O’Brien, 1987, Clinica chimica acta; international journal of clinical chemistry.

The effect of respiratory chain impairment of beta-oxidation in rat heart mitochondria.

S. Eaton, M. Pourfarzam, K. Bartlett, 1996, The Biochemical journal.

Brain indoles in human hepatic encephalopathy

P. Ince, C. Record, K. Bartlett, 1993, Hepatology.

Intermediates of beta-oxidation.

N. Watmough, K. Bartlett, A. G. Causey, 1988, Biochemical Society transactions.

Effect of oral antibiotics on intestinal production of propionic acid

K. Bartlett, A. Mellon, S. Deshpande, 2000, Archives of disease in childhood.

Non-glucose metabolism in cancer cells—is it all in the fat?

J. Lunec, S. Biswas, K. Bartlett, 2012, Cancer and Metastasis Reviews.

beta-Oxidation in human alcoholic and non-alcoholic hepatic steatosis.

S. Eaton, C. Record, K. Bartlett, 1996, Clinical science.

Hypocholesterolaemia in chronic Hepatitis C virus (HCV) infection – Reduced production or increased LDL clearance?

N. Seidah, J. Davignon, M. Bassendine, 2010 .

Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency

Alan Craft, Morteza Pourfarzam, A. Craft, 2001, The Lancet.

Recent developments in the detection of inherited disorders of mitochondrial beta-oxidation.

M. Pourfarzam, K. Bartlett, 1998, Biochemical Society transactions.

Intermediates of mitochondrial beta-oxidation.

S. Eaton, K. Bartlett, 1994, Biochemical Society transactions.