Clayton PT - Search Results

1

Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates.

Sequeira JS, Vellodi A, Vanier MT, Clayton PT. Sequeira JS, et al. Among authors: clayton pt. J Inherit Metab Dis. 1998 Apr;21(2):149-54. doi: 10.1023/a:1005395709826. J Inherit Metab Dis. 1998. PMID: 9584266

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

3 beta-hydroxy-delta 5-C27-steroid dehydrogenase deficiency; effect of chenodeoxycholic acid therapy on liver histology.

Horslen SP, Lawson AM, Malone M, Clayton PT. Horslen SP, et al. Among authors: clayton pt. J Inherit Metab Dis. 1992;15(1):38-46. doi: 10.1007/BF01800342. J Inherit Metab Dis. 1992. PMID: 1583874

4

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.

5

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.

6

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.

7

Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome.

Clayton PT, Kalter DC, Atherton DJ, Besley GT, Broadhead DM. Clayton PT, et al. J Inherit Metab Dis. 1989;12 Suppl 2:358-60. doi: 10.1007/BF03335422. J Inherit Metab Dis. 1989. PMID: 2512444 No abstract available.

8

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.

9

Phytanic acid alpha-oxidase deficiency (Refsum disease) presenting in infancy.

Herbert MA, Clayton PT. Herbert MA, et al. Among authors: clayton pt. J Inherit Metab Dis. 1994;17(2):211-4. doi: 10.1007/BF00711620. J Inherit Metab Dis. 1994. PMID: 7526031

10

Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay.

Clayton PT, Eckhardt S, Wilson J, Hall CM, Yousuf Y, Wanders RJ, Schutgens RB. Clayton PT, et al. J Inherit Metab Dis. 1994;17(5):533-40. doi: 10.1007/BF00711587. J Inherit Metab Dis. 1994. PMID: 7530787

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