Turnbull DM - Search Results

1

Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.

Watmough NJ, Bindoff LA, Birch-Machin MA, Jackson S, Bartlett K, Ragan CI, Poulton J, Gardiner RM, Sherratt HS, Turnbull DM. Watmough NJ, et al. Among authors: turnbull dm. J Clin Invest. 1990 Jan;85(1):177-84. doi: 10.1172/JCI114409. J Clin Invest. 1990. PMID: 2153151 Free PMC article.

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. Among authors: turnbull dm. 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

The sequence of the flavoprotein subunit of bovine heart succinate dehydrogenase.

Birch-Machin MA, Farnsworth L, Ackrell BA, Cochran B, Jackson S, Bindoff LA, Aitken A, Diamond AG, Turnbull DM. Birch-Machin MA, et al. Among authors: turnbull dm. J Biol Chem. 1992 Jun 5;267(16):11553-8. J Biol Chem. 1992. PMID: 1375942 Free article.

4

Combined enzyme defect of mitochondrial fatty acid oxidation.

Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM. Jackson S, et al. Among authors: turnbull dm. J Clin Invest. 1992 Oct;90(4):1219-25. doi: 10.1172/JCI115983. J Clin Invest. 1992. PMID: 1401059 Free PMC article.

5

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

Howell N, Halvorson S, Kubacka I, McCullough DA, Bindoff LA, Turnbull DM. Howell N, et al. Among authors: turnbull dm. Hum Genet. 1992 Sep-Oct;90(1-2):117-20. doi: 10.1007/BF00210753. Hum Genet. 1992. PMID: 1427765

6

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets.

Taylor RW, Jackson S, Pourfarzam M, Bartlett K, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

7

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. Among authors: turnbull dm. Prog Clin Biol Res. 1992;375:327-37. Prog Clin Biol Res. 1992. PMID: 1438378 No abstract available.

8

The measurement of mitochondrial beta-oxidation by release of 3H2O from [9,10-3H]hexadecanoate: application to skeletal muscle and the use of inhibitors as models of metabolic disease.

Kler RS, Sherratt HS, Turnbull DM. Kler RS, et al. Among authors: turnbull dm. Biochem Med Metab Biol. 1992 Apr;47(2):145-56. doi: 10.1016/0885-4505(92)90018-t. Biochem Med Metab Biol. 1992. PMID: 1515172

9

Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic diet.

Wijburg FA, Barth PG, Bindoff LA, Birch-Machin MA, van der Blij JF, Ruitenbeek W, Turnbull DM, Schutgens RB. Wijburg FA, et al. Among authors: turnbull dm. Neuropediatrics. 1992 Jun;23(3):147-52. doi: 10.1055/s-2008-1071331. Neuropediatrics. 1992. PMID: 1641082

10

Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study.

Bindoff LA, Desnuelle C, Birch-Machin MA, Pellissier JF, Serratrice G, Dravet C, Bureau M, Howell N, Turnbull DM. Bindoff LA, et al. Among authors: turnbull dm. J Neurol Sci. 1991 Mar;102(1):17-24. doi: 10.1016/0022-510x(91)90088-o. J Neurol Sci. 1991. PMID: 1649912 Review.

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