Turnbull DM - Search Results

1

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.

Lax NZ, Whittaker RG, Hepplewhite PD, Reeve AK, Blakely EL, Jaros E, Ince PG, Taylor RW, Fawcett PR, Turnbull DM. Lax NZ, et al. Among authors: turnbull dm. Brain. 2012 Jan;135(Pt 1):62-71. doi: 10.1093/brain/awr326. Epub 2011 Dec 20. Brain. 2012. PMID: 22189570 Free PMC article.

2

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

3

Lipid storage myopathy associated with low acyl-CoA dehydrogenase activities.

Turnbull DM, Shepherd IM, Ashworth B, Bartlett K, Johnson MA, Cullen MJ, Jackson S, Sherratt HS. Turnbull DM, et al. Brain. 1988 Aug;111 ( Pt 4):815-28. doi: 10.1093/brain/111.4.815. Brain. 1988. PMID: 3042086

4

Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain.

Morris AA, Taylor RW, Birch-Machin MA, Jackson MJ, Coulthard MG, Bindoff LA, Welch RJ, Howell N, Turnbull DM. Morris AA, et al. Among authors: turnbull dm. Pediatr Nephrol. 1995 Aug;9(4):407-11. doi: 10.1007/BF00866711. Pediatr Nephrol. 1995. PMID: 7577396

5

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. Among authors: turnbull dm. 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.

6

Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients.

Jackson MJ, Schaefer JA, Johnson MA, Morris AA, Turnbull DM, Bindoff LA. Jackson MJ, et al. Among authors: turnbull dm. Brain. 1995 Apr;118 ( Pt 2):339-57. doi: 10.1093/brain/118.2.339. Brain. 1995. PMID: 7735877

7

Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.

Jackson MJ, Bindoff LA, Weber K, Wilson JN, Ince P, Alberti KG, Turnbull DM. Jackson MJ, et al. Among authors: turnbull dm. Diabetes Care. 1994 Jul;17(7):728-33. doi: 10.2337/diacare.17.7.728. Diabetes Care. 1994. PMID: 7924787

8

Complex aetiology of type 2 diabetes.

Walker M, Taylor R, Armstrong M, Turnbull DM. Walker M, et al. Among authors: turnbull dm. Br J Hosp Med. 1994 Aug 17-Sep 6;52(4):179. Br J Hosp Med. 1994. PMID: 8000686 No abstract available.

9

The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria. Implications for our understanding of mitochondrial cytopathies in man.

Taylor RW, Birch-Machin MA, Bartlett K, Lowerson SA, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. J Biol Chem. 1994 Feb 4;269(5):3523-8. J Biol Chem. 1994. PMID: 8106394 Free article.

10

Defects of oxidative phosphorylation in man.

Taylor RW, Birch-Machin MA, Lowerson S, Sherratt HS, West IC, Bartlett K, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. Biochem Soc Trans. 1993 Aug;21 ( Pt 3)(3):804-7. doi: 10.1042/bst0210804. Biochem Soc Trans. 1993. PMID: 8224514 Review. No abstract available.

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