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Rodney Pollitt

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Rodney J Pollitt
Commentary: What degree of hyperphenylalaninaemia requires treatment?
Rodney J Pollitt
New technologies extend the scope of newborn blood-spot screening, but old problems remain unresolved.
Rodney J Pollitt; Jerry K Wales
Newborn screening for congenital hypothyroidism: improved assay performance has created an evidence gap.

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2012: Rodney J Pollitt
Commentary: What degree of hyperphenylalaninaemia requires treatment?
Journal of inherited metabolic disease 2012;35(5):927-30.
2010: Rodney J Pollitt
New technologies extend the scope of newborn blood-spot screening, but old problems remain unresolved.
Acta paediatrica (Oslo, Norway : 1992) 2010;99(12):1766-72.
2010: Rodney J Pollitt; Jerry K Wales
Newborn screening for congenital hypothyroidism: improved assay performance has created an evidence gap.
Journal of inherited metabolic disease 2010;33(Suppl 2):S201-3.
2009: Rodney J Pollitt
Newborn blood spot screening: new opportunities, old problems.
Journal of inherited metabolic disease 2009;32(3):395-9.
2009: Carlo Castellani; Kevin W Southern; Keith Brownlee; Jeannette Dankert Roelse; Alistair Duff; Michael Farrell; Anil Mehta; Anne Munck; Rodney J Pollitt; Isabelle Sermet-Gaudelus; Bridget Wilcken; Manfred Ballmann; Carlo Corbetta; Isabelle de Monestrol; Philip Farrell; Maria Feilcke; Claude Férec; Silvia Gartner; Kevin Gaskin; Jutta Hammermann; Nataliya Kashirskaya; Gerard Loeber; Milan Macek Jr.; Gita Mehta; Andreas Reiman; Paolo Rizzotti; Alec Sammon; Dorota Sands; Alan Smyth; Olaf Sommerburg; Toni Torresani; Georges Travert; Annette Vernooij; Stuart Elborn
European best practice guidelines for cystic fibrosis neonatal screening.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2009;8(3):153-73.
2008: Rodney J Pollitt
External Quality Assurance of laboratory analyses.
Journal of inherited metabolic disease 2008;31(6):659-60.
2008: Verena Peters; S F Garbade; C D Langhans; Georg F Hoffmann; Rodney J Pollitt; M Downing; J R Bonham
Qualitative urinary organic acid analysis: methodological approaches and performance.
Journal of inherited metabolic disease 2008;31(6):690-6.
2008: Melanie Downing; Rodney J Pollitt
Newborn bloodspot screening in the UK--past, present and future.
Annals of clinical biochemistry 2008;45(Pt 1):11-7.
2007: Rodney J Pollitt
Introducing new screens: why are we all doing different things?
Journal of inherited metabolic disease 2007;30(4):423-9.
2007: Rodney J Pollitt; A J Matthews
Population quantile-quantile plots for monitoring assay performance in newborn screening.
Journal of inherited metabolic disease 2007;30(4):607.
2007: Kevin W Southern; Anne Munck; Rodney J Pollitt; Georges Travert; Luisa Zanolla; Jeannette Dankert-Roelse; Carlo Castellani
A survey of newborn screening for cystic fibrosis in Europe.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2007;6(1):57-65.
2006: Rodney J Pollitt
International perspectives on newborn screening.
Journal of inherited metabolic disease 2006;29(2-3):390-6.
2006: Scott D Grosse; Muin J Khoury; Carol L Greene; Krista S Crider; Rodney J Pollitt
The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an update.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(4):205-12.
2004: Rodney J Pollitt; Mark Sharrard
Treating rare inborn errors of metabolism.
Lancet 2004;364(9452):2158-60.
2004: Rodney J Pollitt
Compliance with science: consent or coercion in newborn screening.
European journal of pediatrics 2004;163(12):757-8.
2003: Vanessa Chambers; Lindsey Sutherland; Karren Palmer; Ann Dalton; Alan S Rigby; Robert Sokol; Rodney J Pollitt; Stuart Tanner; Dermot Gleeson
Haemochromatosis-associated HFE genotypes in English blood donors: age-related frequency and biochemical expression.
Journal of hepatology 2003;39(6):925-31.
2003: Rodney J Pollitt
Newborn screening for cystic fibrosis: science, legislation, and human values.
Journal of inherited metabolic disease 2003;26(8):725-7.
2003: Simon E Olpin; A Afifi; S Clark; NJ Manning; James R Bonham; A Dalton; J V Leonard; JM Land; Brage S Andresen; Andrew A M Morris; F Muntoni; D Turnbull; Morteza Pourfarzam; S Rahman; Rodney J Pollitt
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency.
Journal of inherited metabolic disease 2003;26(6):543-57.
2002: Simon E Olpin; Rodney J Pollitt; J McMenamin; NJ Manning; G T N Besley; J P N Ruiter; R J A Wanders
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old man.
Journal of inherited metabolic disease 2002;25(6):477-82.
2002: Anne-Marie Lamhonwah; Simon E Olpin; Rodney J Pollitt; Christine Vianey-Saban; Priscille Divry; Nathalie Guffon; G T N Besley; Russell Onizuka; Linda De Meirleir; Ljerka Cvitanovic-Sojat; Ivo Baric; Carlo Dionisi Vici; Ksenija Fumic; Miljenka Maradin; Ingrid Tein
Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy.
American journal of medical genetics 2002;111(3):271-84.
2001: Rodney J Pollitt
Newborn mass screening versus selective investigation: benefits and costs.
Journal of inherited metabolic disease 2001;24(2):299-302.
2001: Simon E Olpin; J Allen; James R Bonham; S Clark; P T Clayton; J Calvin; Melanie Downing; K Ives; S Jones; NJ Manning; Rodney J Pollitt; S J Standing; M Stuart Tanner
Features of carnitine palmitoyltransferase type I deficiency.
Journal of inherited metabolic disease 2001;24(1):35-42.
2000: NJ Manning; Simon E Olpin; Rodney J Pollitt; Melanie Downing; A F Heeley; I D Young
Fumarate hydratase deficiency: increased fumaric acid in amniotic fluid of two affected pregnancies.
Journal of inherited metabolic disease 2000;23(7):757-9.
2000: J Boyne; S Evans; Rodney J Pollitt; C J Taylor; A Dalton
Many deltaF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation.
Journal of medical genetics 2000;37(7):543-7.
2000: Ken L Chambliss; R G Gray; G Rylance; Rodney J Pollitt; K M Gibson
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency.
Journal of inherited metabolic disease 2000;23(5):497-504.
2000: M J Nowaczyk; Donald T Whelan; R E Hill; Joe T R Clarke; Rodney J Pollitt
Long-chain hydroxydicarboxylic aciduria, carnitine depletion and acetaminophen exposure.
Journal of inherited metabolic disease 2000;23(2):188-9.
1999: Rodney J Pollitt
Principles and performance: assessing the evidence.
Acta paediatrica (Oslo, Norway : 1992). Supplement 1999;88(432):110-4.
1999: Rodney J Pollitt
Tandem mass spectrometry screening: proving effectiveness.
Acta paediatrica (Oslo, Norway : 1992). Supplement 1999;88(432):40-4.
1999: A Green; Rodney J Pollitt
Population newborn screening for inherited metabolic disease: current UK perspectives.
Journal of inherited metabolic disease 1999;22(4):572-9.
1999: Melanie Downing; JC Allen; James R Bonham; Robert G Edwards; NJ Manning; Simon E Olpin; Rodney J Pollitt
Problems in the detection of fatty acid oxidation defects: experience of a quality assurance programme for qualitative urinary organic acid analysis.
Journal of inherited metabolic disease 1999;22(3):289-92.
1999: NJ Manning; James R Bonham; Melanie Downing; Robert G Edwards; Simon E Olpin; Rodney J Pollitt; Morteza Pourfarzam; Mark Sharrard; M Stuart Tanner
Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II.
Journal of inherited metabolic disease 1999;22(1):88-9.
1999: Simon E Olpin; NJ Manning; Rodney J Pollitt; James R Bonham; Melanie Downing; S Clark
The use of [9,10-3H]myristate, [9,10-3H]palmitate and [9,10-3H]oleate for the detection and diagnosis of medium and long-chain fatty acid oxidation disorders in intact cultured fibroblasts.
Advances in experimental medicine and biology 1999;466():321-5.
1998: Rodney J Pollitt; J V Leonard
Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UK.
Archives of disease in childhood 1998;79(2):116-9.
1998: E M Coughlin; E Christensen; P L Kunz; Kalpathy S Krishnamoorthy; V Walker; N R Dennis; R A Chalmers; O N Elpeleg; Donald T Whelan; Rodney J Pollitt; V Ramesh; Roseann Mandell; Vivian E Shih
Molecular analysis and prenatal diagnosis of human fumarase deficiency.
Molecular genetics and metabolism 1998;63(4):254-62.
1997: Simon E Olpin; James R Bonham; Melanie Downing; NJ Manning; Rodney J Pollitt; Mark Sharrard; M Stuart Tanner
Carnitine-acylcarnitine translocase deficiency--a mild phenotype.
Journal of inherited metabolic disease 1997;20(5):714-5.
1997: Simon E Olpin; NJ Manning; Rodney J Pollitt; S Clarke
Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid.
Journal of inherited metabolic disease 1997;20(3):415-9.
1997: H R Seddon; G Gray; Rodney J Pollitt; A Iitiä; A Green
Population screening for the common G985 mutation causing medium-chain acyl-CoA dehydrogenase deficiency with Eu-labeled oligonucleotides and the DELFIA system.
Clinical chemistry 1997;43(3):436-42.
1997: Rodney J Pollitt; A Green; C J McCabe; Andrew Booth; N J Cooper; J V Leonard; Jon P Nicholl; P Nicholson; J R Tunaley; N K Virdi
Neonatal screening for inborn errors of metabolism: cost, yield and outcome.
Health technology assessment (Winchester, England) 1997;1(7):i-iv, 1-202.
1997: Rodney J Pollitt; A Dalton; S Evans; H N Hughes; D Curtis
Neonatal screening for cystic fibrosis in the Trent region (UK): two-stage immunoreactive trypsin screening compared with a three-stage protocol with DNA analysis as an intermediate step.
Journal of medical screening 1997;4(1):23-8.
1996: Michael J Bennett; Daniel Hale; Rodney J Pollitt; C A Stanley; S Variend
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter.
Clinical cardiology 1996;19(3):243-6.
1995: A Streetly; C Grant; Rodney J Pollitt; G M Addison
Survey of scope of neonatal screening in the United Kingdom.
BMJ (Clinical research ed.) 1995;311(7007):726.
1995: S A Lynch; D de Berker; Alan Lehmann; Rodney J Pollitt; M M Reid; W H Lamb
Trichothiodystrophy with sideroblastic anaemia and developmental delay.
Archives of disease in childhood 1995;73(3):249-51.
1995: H R Seddon; A Green; R G Gray; J V Leonard; Rodney J Pollitt
Regional variations in medium-chain acyl-CoA dehydrogenase deficiency.
Lancet 1995;345(8942):135-6.
1995: Rodney J Pollitt
Disorders of mitochondrial long-chain fatty acid oxidation.
Journal of inherited metabolic disease 1995;18(4):473-90.
1994: N J Manning; N P Davies; Simon E Olpin; K H Carpenter; M F Smith; Rodney J Pollitt; S L Duncan; A Larsson; B Carlsson
Prenatal diagnosis of glutathione synthase deficiency.
Prenatal diagnosis 1994;14(6):475-8.
1994: James R Bonham; Melanie Downing; Rodney J Pollitt; NJ Manning; K H Carpenter; Simon E Olpin; JC Allen; E Worthy
Quality assessment of urinary organic acid analysis.
Annals of clinical biochemistry 1994;31 ( Pt 2)():129-33.
1994: John Tolmie; D de Berker; R Dawber; C Galloway; D W Gregory; Alan Lehmann; J McClure; Rodney J Pollitt; John Stephenson
Syndromes associated with trichothiodystrophy.
Clinical dysmorphology 1994;3(1):1-14.
1994: C H Cromby; NJ Manning; Rodney J Pollitt; S Powell; M J Bennett
6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemia.
Journal of inherited metabolic disease 1994;17(1):81-4.
1994: Rodney J Pollitt; NJ Manning; Simon E Olpin; I D Young
Prenatal diagnosis of a defect in medium-chain fatty acid oxidation.
Journal of inherited metabolic disease 1994;17(3):279-82.
1993: C J Taylor; Simon E Olpin; J Rattenbury; A Whippey; C Lunt; N Beckles-Willson; J Higginbottom; Rodney J Pollitt; J Bonham; L S Taitz
Familial hypercholesterolaemia: pilot study to identify children at risk.
Journal of clinical pathology 1993;46(8):730-3.
1993: Rodney J Pollitt
Neonatal screening.
Journal of clinical pathology 1993;46(6):497-9.
1993: R Moore; J F Glasgow; M A Bingham; J A Dodge; Rodney J Pollitt; Simon E Olpin; B Middleton; K Carpenter
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient.
European journal of pediatrics 1993;152(5):433-6.
1993: K Carpenter; Rodney J Pollitt; B Middleton
A unique, membrane-bound, multifunctional enzyme from human liver mitochondria catalysing three steps of fatty acid beta-oxidation.
Biochemical Society transactions 1993;21(1):35S.
1993: Rodney J Pollitt
Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death.
Pädiatrie und Pädologie 1993;28(1):13-7.
1992: S Lowes; M E Rose; Graham A Mills; Rodney J Pollitt
Identification of urinary acylcarnitines using gas chromatography-mass spectrometry: preliminary clinical applications.
Journal of chromatography 1992;577(2):205-14.
1992: K Carpenter; Rodney J Pollitt; B Middleton
Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria.
Biochemical and biophysical research communications 1992;183(2):443-8.
1992: K Carpenter; B Middleton; Rodney J Pollitt
Purification of long-chain 3-hydroxyacyl-CoA dehydrogenase from human infant liver.
Progress in clinical and biological research 1992;375():75-84.
1992: D Curtis; A I Blakemore; Paul C Engel; S Kolvraa; Niels Gregersen; Rodney J Pollitt
Medium chain acyl-CoA dehydrogenase deficiency in the United Kingdom.
Progress in clinical and biological research 1992;375():489-94.
1992: France Demaugre; Jean-Paul Bonnefont; Michèle Brivet; Claude Cepanec; Rodney J Pollitt; B L Priestley; J M Saudubray; J P Leroux
Pathophysiological approach to carnitine palmitoyltransferase II deficiencies.
Progress in clinical and biological research 1992;375():301-8.
1992: Simon E Olpin; NJ Manning; K Carpenter; B Middleton; Rodney J Pollitt
Differential diagnosis of hydroxydicarboxylic aciduria based on release of 3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblasts.
Journal of inherited metabolic disease 1992;15(6):883-90.
1991: S Jackson; K Bartlett; J Land; E R Moxon; Rodney J Pollitt; James V Leonard; Douglass M Turnbull
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
Pediatric research 1991;29(4 Pt 1):406-11.
1991: A I Blakemore; H Singleton; Rodney J Pollitt; Paul C Engel; S Kolvraa; Niels Gregersen; D Curtis
Frequency of the G985 MCAD mutation in the general population.
Lancet 1991;337(8736):298-9.
1991: M J Bennett; Rodney J Pollitt; S I Goodman; Daniel Hale; J Vamecq
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.
Journal of inherited metabolic disease 1991;14(2):165-73.
1991: A Green; M A Preece; C de Sousa; Rodney J Pollitt
Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).
Journal of inherited metabolic disease 1991;14(5):691-7.
1991: K Carpenter; B Middleton; Rodney J Pollitt
The long-chain 3-hydroxyacyl-CoA dehydrogenase of human liver mitochondria.
Journal of inherited metabolic disease 1991;14(3):321-4.
1990: M J Bennett; Rodney J Pollitt; L S Taitz; S Variend
Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death.
Clinical chemistry 1990;36(9):1695-7.
1990: Yoichi Matsubara; Kuniaki Narisawa; Shigeaki Miyabayashi; K Tada; P M Coates; C Bachmann; Louis J Elsas; Rodney J Pollitt; W J Rhead; C R Roe
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.
Biochemical and biophysical research communications 1990;171(1):498-505.
1990: James R Bonham; T J Stephenson; K H Carpenter; J M Rattenbury; C H Cromby; Rodney J Pollitt; D Hull
D(+)-glyceric aciduria: etiology and clinical consequences.
Pediatric research 1990;28(1):38-41.
1990: Serge Przedborski; A Ferster; S Goldman; R Wolter; M Song; T Tonnesen; Rodney J Pollitt; E Vamos
Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings.
American journal of medical genetics 1990;35(4):566-73.
1990: Rodney J Pollitt
Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria.
Progress in clinical and biological research 1990;321():495-502.
1990: M J Bennett; F Allison; Rodney J Pollitt; S Variend
Fatty acid oxidation defects as causes of unexpected death in infancy.
Progress in clinical and biological research 1990;321():349-64.
1990: M J Bennett; P M Coates; Daniel Hale; D S Millington; Rodney J Pollitt; P Rinaldo; C R Roe; K Tanaka
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease 1990;13(5):707-15.
1990: F Allison; M J Bennett; Rodney J Pollitt; S Variend
Acquired deficiency of long-chain acyl-CoA dehydrogenase in liver: a cautionary tale.
Journal of inherited metabolic disease 1990;13(3):333-6.
1990: Graham A Mills; V Walker; M R Ashton; N J Manning; Rodney J Pollitt
Vitreous humour organic acids in medium chain acyl-CoA dehydrogenase deficiency.
Journal of inherited metabolic disease 1990;13(2):239-40.
1990: NJ Manning; Simon E Olpin; Rodney J Pollitt; J Webley
A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts.
Journal of inherited metabolic disease 1990;13(1):58-68.
1989: R E McKerrell; William F Blakemore; M Fred Heath; J Plumb; M J Bennett; Rodney J Pollitt; Christopher J Danpure
Primary hyperoxaluria (L-glyceric aciduria) in the cat: a newly recognised inherited disease.
The Veterinary record 1989;125(2):31-4.
1989: James R Bonham; J M Rattenbury; A Meeks; Rodney J Pollitt
Pyroglutamicaciduria from vigabatrin.
Lancet 1989;1(8652):1452-3.
1989: E M Layward; M S Tanner; Rodney J Pollitt; K Bartlett
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency presenting as a Reye syndrome-like illness.
Journal of inherited metabolic disease 1989;12(3):339-40.
1989: Melanie Downing; P Rose; M J Bennett; NJ Manning; Rodney J Pollitt
Generalised dicarboxylic aciduria: a common finding in neonates.
Journal of inherited metabolic disease 1989;12 Suppl 2():321-4.
1989: Rodney J Pollitt
Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death.
Journal of inherited metabolic disease 1989;12 Suppl 1():215-30.
1988: J F Brookfield; Rodney J Pollitt; I D Young
Family size limitation: a method for demonstrating recessive inheritance.
Journal of medical genetics 1988;25(3):181-5.
1988: William F Blakemore; M Fred Heath; M J Bennett; C H Cromby; Rodney J Pollitt
Primary hyperoxaluria and L-glyceric aciduria in the cat.
Journal of inherited metabolic disease 1988;11 Suppl 2():215-7.
1987: Rodney J Pollitt; B Fowler; I B Sardharwalla; M A Edwards; R G Gray
Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gut.
Clinica chimica acta; international journal of clinical chemistry 1987;169(2-3):151-7.
1987: Rodney J Pollitt
Endogenous catabolism as source of toxic metabolites in isovaleric acidemia.
The Journal of pediatrics 1987;111(3):477-8.
1987: R G Gray; Rodney J Pollitt; J Webley
Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblasts.
Biochemical medicine and metabolic biology 1987;38(1):121-4.
1987: M J Bennett; F Allison; Rodney J Pollitt; N J Manning; R G Gray; A Green; Daniel Hale; P M Coates
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.
Lancet 1987;1(8530):440-1.
1987: M J Bennett; F Allison; G W Lowther; R G Gray; D I Johnston; J S Fitzsimmons; N J Manning; Rodney J Pollitt
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.
Prenatal diagnosis 1987;7(2):135-41.
1987: Rodney J Pollitt
Inherited disorders of straight chain fatty acid oxidation.
Archives of disease in childhood 1987;62(1):6-7.
1987: B E Barwell; Rodney J Pollitt
[Attitude of parents toward the prenatal diagnosis of phenylketonuria].
Archives françaises de pédiatrie 1987;44 Suppl 1():665-6.
1987: G K Brown; C H Cromby; NJ Manning; Rodney J Pollitt
Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidation.
Journal of inherited metabolic disease 1987;10(4):367-75.
1987: M J Bennett; E Worthy; Rodney J Pollitt
The incidence and presentation of dicarboxylic aciduria.
Journal of inherited metabolic disease 1987;10(3):241-2.
1987: M J Bennett; Rodney J Pollitt; J M Land; M J Turner; C H Cheetham
Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic features.
Journal of inherited metabolic disease 1987;10(1):95-6.
1986: M J Bennett; S Variend; Rodney J Pollitt
Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant death.
Lancet 1986;2(8521-22):1470.
1986: M J Bennett; Neil Marlow; Rodney J Pollitt; J K Wales
Glutaric aciduria type 1: biochemical investigations and postmortem findings.
European journal of pediatrics 1986;145(5):403-5.
1985: N J Manning; Rodney J Pollitt
Tracer studies of the interconversion of R- and S-methylmalonic semialdehydes in man.
The Biochemical journal 1985;231(2):481-4.
1985: Rodney J Pollitt; A Green; R Smith
Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes.
Journal of inherited metabolic disease 1985;8(2):75-9.
1985: A Green; T G Marshall; M J Bennett; R G Gray; Rodney J Pollitt
Riboflavin-responsive ethylmalonic-adipic aciduria.
Journal of inherited metabolic disease 1985;8(2):67-70.
1985: A Sahota; J A Blair; P A Barford; R J Leeming; A Green; Rodney J Pollitt
Neonatal screening for dihydropteridine reductase deficiency.
Journal of inherited metabolic disease 1985;8 Suppl 2():99-100.
1985: M J Bennett; R G Gray; D M Isherwood; N Murphy; Rodney J Pollitt
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect.
Journal of inherited metabolic disease 1985;8 Suppl 2():135-6.
1984: M J Bennett; A Green; Rodney J Pollitt; E Worthy
The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year period.
Annals of clinical biochemistry 1984;21 ( Pt 1)():45-50.
1984: K Bartlett; M J Bennett; R P Hill; L S Lashford; Rodney J Pollitt; H G Worth
Isolated biotin-resistant 3-methylcrotonyl CoA carboxylase deficiency presenting with life-threatening hypoglycaemia.
Journal of inherited metabolic disease 1984;7(4):182.
1984: M J Bennett; D A Curnock; P C Engel; L Shaw; R G Gray; D Hull; A D Patrick; Rodney J Pollitt
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally.
Journal of inherited metabolic disease 1984;7(2):57-61.
1983: Rodney J Pollitt
The occurrence of substituted 3-methyl-3-hydroxyglutaric acids in urine in propionic acidaemia and in beta-ketothiolase deficiency.
Biomedical mass spectrometry 1983;10(4):253-7.
1983: M J Bennett; J M Littlewood; A MacDonald; Rodney J Pollitt; J Thompson
A case of beta-ketothiolase deficiency.
Journal of inherited metabolic disease 1983;6(4):157.
1983: R G Gray; S E Hill; Rodney J Pollitt
Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuria.
Journal of inherited metabolic disease 1983;6(4):143-8.
1983: Rodney J Pollitt
Neonatal screening in France.
Journal of inherited metabolic disease 1983;6(2):49-50.
1982: L Stankler; D Lloyd; Rodney J Pollitt; E S Gray; H Thom; G Russell
Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndrome.
Archives of disease in childhood 1982;57(3):212-6.
1982: R G Gray; S E Hill; Rodney J Pollitt
Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria.
Clinica chimica acta; international journal of clinical chemistry 1982;118(2-3):141-8.
1981: P J Congdon; D Haigh; R Smith; A Green; Rodney J Pollitt
Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby.
Journal of inherited metabolic disease 1981;4(2):79-80.
1980: J P Farriaux; J L Dhondt; Rodney J Pollitt
Detection of carbamyl phosphate synthetase 1 deficiency using duodenal biopsy samples.
Archives of disease in childhood 1980;55(10):826-7.
1980: D C Watts; E O Anosike; B Moreland; Rodney J Pollitt; Christopher Lee
The use of arginine analogues for investigating the functional organization of the arginine-binding site in lobster muscle arginine kinase. Role of the 'essential' thiol group.
The Biochemical journal 1980;185(3):593-9.
1980: R G Gray; E M O'Neill; Rodney J Pollitt
Alpha-aminoadipic aciduria: chemical and enzymatic studies.
Journal of inherited metabolic disease 1980;2(4):89-92.
1980: Rodney J Pollitt; B Sandhu
Ascorbic acid: an unstable ninhydrin-positive urinary constituent running with valine in a commonly used screening system.
Journal of inherited metabolic disease 1980;3(1):17-8.
1979: S E Hill; F A Jenner; Christopher Lee; C Paschalis; Rodney J Pollitt; G A Sampson
Urinary dicarboxylic acids in patients receiving lithium or rubidium salts.
Psychopharmacology 1979;65(1):85-7.
1979: H Peck; Rodney J Pollitt
The occurrence of gamma-glutamylphenylalanine in the urine of newborn phenylketonurics.
Clinica chimica acta; international journal of clinical chemistry 1979;94(3):237-40.
1979: Rodney J Pollitt
Investigation of atypical phenylketonuria.
Lancet 1979;1(8116):618.
1978: V Fell; Rodney J Pollitt
3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuria.
Clinica chimica acta; international journal of clinical chemistry 1978;87(3):405-9.
1978: J A Hoskins; Rodney J Pollitt
The determination of 5-methoxyindole-3-acetic acid in human urine by mass fragmentography.
Journal of chromatography 1978;145(2):285-9.
1978: Rodney J Pollitt
Loads versus tracers for assessing phenylalanine hydroxylase activity using plasma phenylalanine decay curves.
Clinica chimica acta; international journal of clinical chemistry 1978;83(3):270-2.
1978: V Fell; J A Hoskins; Rodney J Pollitt
The labelling of urinary acids after oral doses of deuterated L-phenylalanine and L-tyrosine in normal subjects. Quantitative studies with implications for the deuterated phenylalanine load test in phenylketonuria.
Clinica chimica acta; international journal of clinical chemistry 1978;83(3):259-69.
1977: J P Farriaux; C Ponte; Rodney J Pollitt; P Lequien; P Formstecher; J L Dhondt
Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptoms.
Acta paediatrica Scandinavica 1977;66(4):529-34.
1977: Rodney J Pollitt; J A Black; R G Gray; V H Lyons
Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratios.
Annals of clinical biochemistry 1977;14(3):139.
1976: R G Gray; J A Black; V H Lyons; Rodney J Pollitt
Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratios.
Pediatric research 1976;10(11):918-23.
1976: R A Jones; Rodney J Pollitt
The hydroxylation of p-tyramine in man.
The Journal of pharmacy and pharmacology 1976;28(5):461-2.
1976: J L Dhondt; J P Farriaux; Rodney J Pollitt; E Vamos; P Richard; D Blanckaert; M Delecour; J C Monnier; G Fontaine
[Attempt at antenatal diagnosis of argininosuccinic aciduria].
Annales de génétique 1976;19(1):23-7.
1976: J P Farriaux; J L Dhondt; P Formstecher; J J Martin; Rodney J Pollitt; J Knit; A Lagrou; Y Mardens; G Fontaine
[Pathological and biochemical studies on a neonatal case of argininosuccinic aciduria (author's transl)].
Acta neurologica Belgica 1976;76(1):26-34.
1975: Christopher Lee; S E Hill; M Dimitrakoudi; F A Jenner; Rodney J Pollitt
The relationship of plasma to erythrocyte lithium levels in patients taking lithium carbonate.
The British journal of psychiatry : the journal of mental science 1975;127():596-8.
1975: J A Hoskins; Rodney J Pollitt
Quantitative aspects of urinary indolo-3-acetic acid and 5-hydroxyindole-3-acetic acid excretion.
Journal of chromatography 1975;109(2):436-8.
1975: V Fell; Christopher Lee; Rodney J Pollitt
The occurrence of (S)-3,4-dihydroxybutyrate in human blood and urine.
Biochemical medicine 1975;13(1):40-5.
1975: E Bailey; P A Bond; B A Brooks; M Dimitrakoudi; F A Jenner; A Judd; Christopher Lee; E A Lenton; S McNeil; Rodney J Pollitt; G A Sampson; E A Thompson
The medicinal chemistry of lithium.
Progress in medicinal chemistry 1975;11():193-272.
1974: Rodney J Pollitt
Phenylpropionic acid in the urine of patients with phenylketonuria and normals.
Clinica chimica acta; international journal of clinical chemistry 1974;55(3):317-22.
1974: Rodney J Pollitt; K M Pretty
The glycoasparagines in urine of a patient with aspartylglycosaminuria.
The Biochemical journal 1974;141(1):141-6.
1974: C W Crane; F A Jenner; Rodney J Pollitt
The relationship between the formation of urea and argininosuccinate in a patient with argininosuccinic aciduria studied with labelled precursors.
Clinical science and molecular medicine 1974;46(6):715-27.
1974: V Fell; Rodney J Pollitt; G A Sampson; T Wright
Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport.
American journal of diseases of children (1960) 1974;127(5):752-6.
1973: J Palo; Rodney J Pollitt; K M Pretty; H Savolainen
Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between English and Finnish patients with special reference to storage materials.
Clinica chimica acta; international journal of clinical chemistry 1973;47(1):69-74.
1973: Rodney J Pollitt
Argininosuccinate lyase levels in blood, liver and cultured fibroblasts of a patient with argininosuccinic aciduria.
Clinica chimica acta; international journal of clinical chemistry 1973;46(1):33-7.
1972: Christopher Lee; Rodney J Pollitt
The estimation of glutarate in urine using gas chromatography mass spectrometry with an internal isotopic standard.
Biochemical medicine 1972;6(6):536-42.
1972: R J Flower; Rodney J Pollitt; P A Sanford; D H Smyth
Metabolism and transfer of choline in hamster small intestine.
The Journal of physiology 1972;226(2):473-89.
1972: P A Bond; F A Jenner; Christopher Lee; E Lenton; Rodney J Pollitt; G A Sampson
The effect of lithium salts on the urinary excretion of -oxoglutarate in man.
British journal of pharmacology 1972;46(1):116-23.
1972: Rodney J Pollitt; K M Pretty
Glycoasparagines in the urine of patients with aspartylglycosaminuria.
The Biochemical journal 1972;128(4):129P-130P.
1972: R J Flower; Rodney J Pollitt; P A Sanford; D H Smyth
The metabolite formed during choline transfer by the intestine.
The Journal of physiology 1972;222(2):146P-147P.
1972: Christopher Lee; Rodney J Pollitt
New derivatives of argininosuccinic acid in the urine of a patient with argininosuccinicaciduria.
The Biochemical journal 1972;126(1):79-87.
1971: Rodney J Pollitt; P D Stonier
Proteins of normal hair and of cystine-deficient hair from mentally retarded siblings.
The Biochemical journal 1971;122(4):433-44.
1970: Christopher Lee; Rodney J Pollitt
The anhydrides of argininosuccinic acid.
Tetrahedron 1970;26(13):3113-21.
1970: J B Garston; R R Gordon; C T Hart; Rodney J Pollitt
An unusual case of homocystinuria.
The British journal of ophthalmology 1970;54(4):248-51.
1969: Rodney J Pollitt; F A Jenner
Enzymatic cleavage of 2-acetamido-1-(beta'-L-aspartamido)-1,2-dideoxy-beta-D-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylglycosaminuria.
Clinica chimica acta; international journal of clinical chemistry 1969;25(3):413-6.
1969: D J Neadle; Rodney J Pollitt
Photolysis of N-2,4-dinitrophenylamino-acids; Structural requirements for the formation of 6-nitrobenzimidazole 1-oxides.
Journal of the Chemical Society. Perkin transactions 1 1969;16():2127-30.
1968: Rodney J Pollitt; F A Jenner; H Merskey
Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
Lancet 1968;2(7562):253-5.
1968: Rodney J Pollitt; F A Jenner; M Davies
Sibs with mental and physical retardation and trichorrhexis nodosa with abnormal amino acid composition of the hair.
Archives of disease in childhood 1968;43(228):211-6.
1967: A A Boulton; Rodney J Pollitt; J R Majer
Identity of a urinary "pink spot" in schizophrenia and Parkinson's disease.
Nature 1967;215(5097):132-4.
1967: D J Neadle; Rodney J Pollitt
The photolysis of N-2,4-dinitrophenylamino-acids to give 2-substituted 6-nitrobenzimidazole 1-oxides.
Journal of the Chemical Society. Perkin transactions 1 1967;18():1764-6.
1966: F E Pittman; Rodney J Pollitt
Studies of jejunal mucosal digestion of peptic-tryptic digests of wheat protein in coeliac disease.
Gut 1966;7(4):368-71.