Clayton PT - Search Results

1

The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra.

Lemonde HA, Johnson AW, Clayton PT. Lemonde HA, et al. Among authors: clayton pt. Rapid Commun Mass Spectrom. 1999;13(12):1159-64. doi: 10.1002/(SICI)1097-0231(19990630)13:12<1159::AID-RCM636>3.0.CO;2-#. Rapid Commun Mass Spectrom. 1999. PMID: 10390861

2

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.

3

Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.

Clayton PT, Patel E, Lawson AM, Carruthers RA, Collins J. Clayton PT, et al. J Clin Invest. 1990 Apr;85(4):1267-73. doi: 10.1172/JCI114563. J Clin Invest. 1990. PMID: 2318981 Free PMC article.

4

Delta 4-3-oxosteroid 5 beta-reductase deficiency: failure of ursodeoxycholic acid treatment and response to chenodeoxycholic acid plus cholic acid.

Clayton PT, Mills KA, Johnson AW, Barabino A, Marazzi MG. Clayton PT, et al. Gut. 1996 Apr;38(4):623-8. doi: 10.1136/gut.38.4.623. Gut. 1996. PMID: 8707100 Free PMC article.

5

The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots.

Johnson AW, Mills K, Clayton PT. Johnson AW, et al. Among authors: clayton pt. Biochem Soc Trans. 1996 Aug;24(3):932-8. doi: 10.1042/bst0240932. Biochem Soc Trans. 1996. PMID: 8878877 No abstract available.

6

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

7

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

8

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.

van Grunsven EG, van Berkel E, Ijlst L, Vreken P, de Klerk JB, Adamski J, Lemonde H, Clayton PT, Cuebas DA, Wanders RJ. van Grunsven EG, et al. Among authors: clayton pt. Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2128-33. doi: 10.1073/pnas.95.5.2128. Proc Natl Acad Sci U S A. 1998. PMID: 9482850 Free PMC article.

9

A method for the quantitation of conjugated bile acids in dried blood spots using electrospray ionization-mass spectrometry.

Mills KA, Mushtaq I, Johnson AW, Whitfield PD, Clayton PT. Mills KA, et al. Among authors: clayton pt. Pediatr Res. 1998 Mar;43(3):361-8. doi: 10.1203/00006450-199803000-00009. Pediatr Res. 1998. PMID: 9505275

10

Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basis.

Van Grunsven EG, van Berkel E, Lemonde H, Clayton PT, Wanders RJ. Van Grunsven EG, et al. Among authors: clayton pt. J Inherit Metab Dis. 1998 Jun;21(3):298-301. doi: 10.1023/a:1005396912015. J Inherit Metab Dis. 1998. PMID: 9686380 No abstract available.

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