Clayton PT - Search Results

1

Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease.

Morris AA, Thekekara A, Wilks Z, Clayton PT, Leonard JV, Aynsley-Green A. Morris AA, et al. Among authors: clayton pt. Arch Dis Child. 1996 Aug;75(2):115-9. doi: 10.1136/adc.75.2.115. Arch Dis Child. 1996. PMID: 8869190 Free PMC article.

2

Liver transplantation in tyrosinaemia type 1: the dilemma of timing the operation.

Salt A, Barnes ND, Rolles K, Calne RY, Clayton PT, Leonard JV. Salt A, et al. Among authors: clayton pt. Acta Paediatr. 1992 May;81(5):449-52. doi: 10.1111/j.1651-2227.1992.tb12270.x. Acta Paediatr. 1992. PMID: 1323361

3

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome.

Horslen SP, Clayton PT, Harding BN, Hall NA, Keir G, Winchester B. Horslen SP, et al. Among authors: clayton pt. Arch Dis Child. 1991 Sep;66(9):1027-32. doi: 10.1136/adc.66.9.1027. Arch Dis Child. 1991. PMID: 1929507 Free PMC article.

4

Mitochondrial phosphoenolpyruvate carboxykinase deficiency.

Leonard JV, Hyland K, Furukawa N, Clayton PT. Leonard JV, et al. Among authors: clayton pt. Eur J Pediatr. 1991 Jan;150(3):198-9. doi: 10.1007/BF01963566. Eur J Pediatr. 1991. PMID: 2044592

5

Ultrastructure of liver in inherited disorders of fat oxidation.

Lake BD, Clayton PT, Leonard JV, Bhuiyan AK, Bartlett K, Green AA. Lake BD, et al. Among authors: clayton pt. Lancet. 1987 Feb 14;1(8529):382-3. doi: 10.1016/s0140-6736(87)91752-1. Lancet. 1987. PMID: 2880182 No abstract available.

6

Mitochondrial phosphoenolpyruvate carboxykinase deficiency.

Clayton PT, Hyland K, Brand M, Leonard JV. Clayton PT, et al. Eur J Pediatr. 1986 Apr;145(1-2):46-50. doi: 10.1007/BF00441851. Eur J Pediatr. 1986. PMID: 3089795

7

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.

Walter JH, Clayton PT, Leonard JV. Walter JH, et al. Among authors: clayton pt. J Inherit Metab Dis. 1986;9(3):287-8. doi: 10.1007/BF01799665. J Inherit Metab Dis. 1986. PMID: 3099075 No abstract available.

8

Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency.

Hyland K, Smith I, Bottiglieri T, Perry J, Wendel U, Clayton PT, Leonard JV. Hyland K, et al. Among authors: clayton pt. Neurology. 1988 Mar;38(3):459-62. doi: 10.1212/wnl.38.3.459. Neurology. 1988. PMID: 3347350

9

Impaired neurotransmitter amine metabolism in arginase deficiency.

Hyland K, Smith I, Clayton PT, Leonard JV. Hyland K, et al. Among authors: clayton pt. J Neurol Neurosurg Psychiatry. 1985 Nov;48(11):1188-9. doi: 10.1136/jnnp.48.11.1188-a. J Neurol Neurosurg Psychiatry. 1985. PMID: 4078590 Free PMC article. No abstract available.

10

Cystic fibrosis presenting as kwashiorkor with florid skin rash.

Phillips RJ, Crock CM, Dillon MJ, Clayton PT, Curran A, Harper JI. Phillips RJ, et al. Among authors: clayton pt. Arch Dis Child. 1993 Oct;69(4):446-8. doi: 10.1136/adc.69.4.446. Arch Dis Child. 1993. PMID: 8259877 Free PMC article.

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