Taylor RW - Search Results

1

A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency.

Deschauer M, Chrzanowska-Lightowlers ZM, Biekmann E, Pourfarzam M, Taylor RW, Turnbull DM, Zierz S. Deschauer M, et al. Among authors: taylor rw. Mol Genet Metab. 2003 Jun;79(2):124-8. doi: 10.1016/s1096-7192(03)00067-2. Mol Genet Metab. 2003. PMID: 12809643

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. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

3

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: taylor rw. Pediatr Nephrol. 1995 Aug;9(4):407-11. doi: 10.1007/BF00866711. Pediatr Nephrol. 1995. PMID: 7577396

4

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: taylor rw. 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.

5

Insulin sensitivity and mitochondrial gene mutation.

Walker M, Taylor RW, Stewart MW, Bindoff LA, Jackson MJ, Alberti GK, Turnbull DM. Walker M, et al. Among authors: taylor rw. Diabetes Care. 1995 Feb;18(2):273-5. doi: 10.2337/diacare.18.2.273. Diabetes Care. 1995. PMID: 7729311 No abstract available.

6

Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency.

Ruitenbeek W, Poels PJ, Turnbull DM, Garavaglia B, Chalmers RA, Taylor RW, Gabreëls FJ. Ruitenbeek W, et al. Among authors: taylor rw. J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):209-14. doi: 10.1136/jnnp.58.2.209. J Neurol Neurosurg Psychiatry. 1995. PMID: 7876853 Free PMC article.

7

Complex aetiology of type 2 diabetes.

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

8

Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.

Taylor RW, Birch-Machin MA, Bartlett K, Turnbull DM. Taylor RW, et al. Biochim Biophys Acta. 1993 Jun 19;1181(3):261-5. doi: 10.1016/0925-4439(93)90030-5. Biochim Biophys Acta. 1993. PMID: 8391327

9

Human insulin receptor substrate-1: variant sequences in familial non-insulin-dependent diabetes mellitus.

Armstrong M, Haldane F, Taylor RW, Humphriss D, Berrish T, Stewart MW, Turnbull DM, Alberti KG, Walker M. Armstrong M, et al. Among authors: taylor rw. Diabet Med. 1996 Feb;13(2):133-8. doi: 10.1002/(SICI)1096-9136(199602)13:2<133::AID-DIA7>3.0.CO;2-2. Diabet Med. 1996. PMID: 8641117

10

Variant sequences of the Hexokinase II gene in familial NIDDM.

Taylor RW, Printz RL, Armstrong M, Granner DK, Alberti KG, Turnbull DM, Walker M. Taylor RW, et al. Diabetologia. 1996 Mar;39(3):322-8. doi: 10.1007/BF00418348. Diabetologia. 1996. PMID: 8721778

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