Clayton PT - Search Results

1

Pyridoxal 5'-phosphate in cerebrospinal fluid; factors affecting concentration.

Footitt EJ, Heales SJ, Mills PB, Allen GF, Oppenheim M, Clayton PT. Footitt EJ, et al. Among authors: clayton pt. J Inherit Metab Dis. 2011 Apr;34(2):529-38. doi: 10.1007/s10545-011-9279-7. Epub 2011 Feb 9. J Inherit Metab Dis. 2011. PMID: 21305354

2

Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome.

Clayton PT, Winchester BG, Keir G. Clayton PT, et al. J Inherit Metab Dis. 1992;15(6):857-61. doi: 10.1007/BF01800221. J Inherit Metab Dis. 1992. PMID: 1293380

3

Aromatic amino acid decarboxylase deficiency in twins.

Hyland K, Clayton PT. Hyland K, et al. Among authors: clayton pt. J Inherit Metab Dis. 1990;13(3):301-4. doi: 10.1007/BF01799380. J Inherit Metab Dis. 1990. PMID: 1700191 No abstract available.

4

Inborn errors of bile acid metabolism.

Clayton PT. Clayton PT. J Inherit Metab Dis. 1991;14(4):478-96. doi: 10.1007/BF01797919. J Inherit Metab Dis. 1991. PMID: 1749214 Review.

5

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation.

Clayton PT, Lake BD, Hjelm M, Stephenson JB, Besley GT, Wanders RJ, Schram AW, Tager JM, Schutgens RB, Lawson AM. Clayton PT, et al. J Inherit Metab Dis. 1988;11 Suppl 2:165-8. doi: 10.1007/BF01804226. J Inherit Metab Dis. 1988. PMID: 3141700 No abstract available.

6

Sanfilippo disease (mucopolysaccharidosis type III) presenting as transient renal tubular dysfunction.

Ramaswami U, Van 't Hoff W, Clayton P, Vellodi A. Ramaswami U, et al. J Inherit Metab Dis. 1996;19(1):87-8. doi: 10.1007/BF01799354. J Inherit Metab Dis. 1996. PMID: 8830184 No abstract available.

7

Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidation.

Clayton PT, Johnson AW, Mills KA, Lynes GW, Wilson J, Casteels M, Mannaerts G. Clayton PT, et al. J Inherit Metab Dis. 1996;19(6):761-8. doi: 10.1007/BF01799170. J Inherit Metab Dis. 1996. PMID: 8982949

8

A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity.

Charlwood J, Clayton P, Johnson A, Keir G, Mian N, Winchester B. Charlwood J, et al. J Inherit Metab Dis. 1997 Nov;20(6):817-26. doi: 10.1023/a:1005380003902. J Inherit Metab Dis. 1997. PMID: 9427152

9

Applications of mass spectrometry in the study of inborn errors of metabolism.

Clayton PT. Clayton PT. J Inherit Metab Dis. 2001 Apr;24(2):139-50. doi: 10.1023/a:1010358715835. J Inherit Metab Dis. 2001. PMID: 11405336 Review.

10

Neonatal presentation of coenzyme Q10 deficiency.

Rahman S, Hargreaves I, Clayton P, Heales S. Rahman S, et al. J Pediatr. 2001 Sep;139(3):456-8. doi: 10.1067/mpd.2001.117575. J Pediatr. 2001. PMID: 11562630

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