Aynsley-Green A - Search Results

1

Inherited defects of mitochondrial fatty acid oxidation.

Turnbull DM, Shepherd IM, Aynsley-Green A. Turnbull DM, et al. Biochem Soc Trans. 1988 Jun;16(3):424-7. doi: 10.1042/bst0160424. Biochem Soc Trans. 1988. PMID: 3181618 No abstract available.

2

The measurement of carnitine and acyl-carnitines: application to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidation.

Bhuiyan AK, Jackson S, Turnbull DM, Aynsley-Green A, Leonard JV, Bartlett K. Bhuiyan AK, et al. Clin Chim Acta. 1992 May 15;207(3):185-204. doi: 10.1016/0009-8981(92)90118-a. Clin Chim Acta. 1992. PMID: 1327583

3

Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.

Jackson S, Kler RS, Bartlett K, Pourfarzam M, Aynsley-Green A, Bindoff LA, Turnbull DM. Jackson S, et al. Prog Clin Biol Res. 1992;375:327-37. Prog Clin Biol Res. 1992. PMID: 1438378 No abstract available.

4

Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain.

Birch-Machin MA, Shepherd IM, Watmough NJ, Sherratt HS, Bartlett K, Darley-Usmar VM, Milligan DW, Welch RJ, Aynsley-Green A, Turnbull DM. Birch-Machin MA, et al. Pediatr Res. 1989 May;25(5):553-9. doi: 10.1203/00006450-198905000-00025. Pediatr Res. 1989. PMID: 2541396

5

Tissue specific defect of complex I of the mitochondrial respiratory chain.

Watmough NJ, Birch-Machin MA, Bindoff LA, Aynsley-Green A, Simpson K, Ragan CI, Sherratt HS, Turnbull DM. Watmough NJ, et al. Biochem Biophys Res Commun. 1989 Apr 28;160(2):623-7. doi: 10.1016/0006-291x(89)92478-9. Biochem Biophys Res Commun. 1989. PMID: 2719685

6

Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractions.

Shepherd IM, Birch-Machin MA, Johnson MA, Sherratt HS, Aynsley-Green A, Droste M, Kadenbach B, Stephenson JB, King MD, Dick DJ, et al. Shepherd IM, et al. J Neurol Sci. 1988 Nov;87(2-3):265-74. doi: 10.1016/0022-510x(88)90251-1. J Neurol Sci. 1988. PMID: 2850350

7

Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complex.

Birch-Machin MA, Shepherd IM, Solomon M, Yeaman SJ, Gardner-Medwin D, Sherratt HS, Lindsay JG, Aynsley-Green A, Turnbull DM. Birch-Machin MA, et al. J Inherit Metab Dis. 1988;11(2):207-17. doi: 10.1007/BF01799876. J Inherit Metab Dis. 1988. PMID: 3139934

8

Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12.

Morris AA, Taylor RW, Lightowlers RN, Aynsley-Green A, Bartlett K, Turnbull DM. Morris AA, et al. Hum Mol Genet. 1995 Apr;4(4):747-9. doi: 10.1093/hmg/4.4.747. Hum Mol Genet. 1995. PMID: 7633427 No abstract available.

9

A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiency.

Bhuiyan AK, Watmough NJ, Turnbull DM, Aynsley-Green A, Leonard JV, Bartlett K. Bhuiyan AK, et al. Clin Chim Acta. 1987 May 29;165(1):39-44. doi: 10.1016/0009-8981(87)90216-6. Clin Chim Acta. 1987. PMID: 3608187

10

Glucose: a fuel for thought!

Aynsley-Green A. Aynsley-Green A. J Paediatr Child Health. 1991 Feb;27(1):21-30. doi: 10.1111/j.1440-1754.1991.tb00340.x. J Paediatr Child Health. 1991. PMID: 1828360 Review. No abstract available.

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