Taylor RW - Search Results

1

Rapid identification of human muscle disease with fibre optic Raman spectroscopy.

Alix JJP, Plesia M, Lloyd GR, Dudgeon AP, Kendall CA, Hewamadduma C, Hadjivassiliou M, McDermott CJ, Gorman GS, Taylor RW, Shaw PJ, Day JCC. Alix JJP, et al. Among authors: taylor rw. Analyst. 2022 May 30;147(11):2533-2540. doi: 10.1039/d1an01932e. Analyst. 2022. PMID: 35545877 Free PMC article.

2

Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis.

Menzies FM, Cookson MR, Taylor RW, Turnbull DM, Chrzanowska-Lightowlers ZM, Dong L, Figlewicz DA, Shaw PJ. Menzies FM, et al. Among authors: taylor rw. Brain. 2002 Jul;125(Pt 7):1522-33. doi: 10.1093/brain/awf167. Brain. 2002. PMID: 12077002

3

Investigation of mitochondrial function in hereditary spastic paraparesis.

McDermott CJ, Taylor RW, Hayes C, Johnson M, Bushby KM, Turnbull DM, Shaw PJ. McDermott CJ, et al. Among authors: taylor rw. Neuroreport. 2003 Mar 3;14(3):485-8. doi: 10.1097/00001756-200303030-00038. Neuroreport. 2003. PMID: 12634509

4

Motor neuron disease in a patient with a mitochondrial tRNAIle mutation.

Borthwick GM, Taylor RW, Walls TJ, Tonska K, Taylor GA, Shaw PJ, Ince PG, Turnbull DM. Borthwick GM, et al. Among authors: taylor rw, taylor ga. Ann Neurol. 2006 Mar;59(3):570-4. doi: 10.1002/ana.20758. Ann Neurol. 2006. PMID: 16358336

5

Investigation of the mitochondrial genome in patients with atypical motor neuron disease.

Phoenix C, Taylor GA, Hartley J, Nixon H, Ince PG, Shaw PJ, Turnbull DM, Taylor RW. Phoenix C, et al. Among authors: taylor rw, taylor ga. J Neurol. 2007 Apr;254(4):482-7. doi: 10.1007/s00415-006-0399-1. Epub 2007 Mar 31. J Neurol. 2007. PMID: 17401521

6

Clinical reasoning: Blurred vision and dancing feet: restless legs syndrome presenting in mitochondrial disease.

Aitken H, Gorman G, McFarland R, Roberts M, Taylor RW, Turnbull DM. Aitken H, et al. Among authors: taylor rw. Neurology. 2009 May 5;72(18):e86-90. doi: 10.1212/WNL.0b013e3181a411b8. Neurology. 2009. PMID: 19414717 No abstract available.

7

Multi-system neurological disease is common in patients with OPA1 mutations.

Yu-Wai-Man P, Griffiths PG, Gorman GS, Lourenco CM, Wright AF, Auer-Grumbach M, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke MP, Dhillon B, Czermin B, Stewart JD, Hudson G, Reynier P, Bonneau D, Marques W Jr, Lenaers G, McFarland R, Taylor RW, Turnbull DM, Votruba M, Zeviani M, Carelli V, Bindoff LA, Horvath R, Amati-Bonneau P, Chinnery PF. Yu-Wai-Man P, et al. Among authors: taylor rw. Brain. 2010 Mar;133(Pt 3):771-86. doi: 10.1093/brain/awq007. Epub 2010 Feb 15. Brain. 2010. PMID: 20157015 Free PMC article.

8

Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3.

Horvath R, Czermin B, Gulati S, Demuth S, Houge G, Pyle A, Dineiger C, Blakely EL, Hassani A, Foley C, Brodhun M, Storm K, Kirschner J, Gorman GS, Lochmüller H, Holinski-Feder E, Taylor RW, Chinnery PF. Horvath R, et al. Among authors: taylor rw. J Neurol Neurosurg Psychiatry. 2012 Feb;83(2):174-8. doi: 10.1136/jnnp-2011-301258. Epub 2011 Oct 29. J Neurol Neurosurg Psychiatry. 2012. PMID: 22036850

9

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.

Hollingsworth KG, Gorman GS, Trenell MI, McFarland R, Taylor RW, Turnbull DM, MacGowan GA, Blamire AM, Chinnery PF. Hollingsworth KG, et al. Among authors: taylor rw. Neuromuscul Disord. 2012 Jul;22(7):592-6. doi: 10.1016/j.nmd.2012.03.001. Epub 2012 Apr 17. Neuromuscul Disord. 2012. PMID: 22513320 Free PMC article.

10

Diagnostic investigations of patients with chronic progressive external ophthalmoplegia.

Yu-Wai-Man P, Gorman GS, Taylor RW, Turnbull DM. Yu-Wai-Man P, et al. Among authors: taylor rw. Br J Ophthalmol. 2012 Dec;96(12):1536. doi: 10.1136/bjophthalmol-2012-302566. Epub 2012 Sep 28. Br J Ophthalmol. 2012. PMID: 23024221 No abstract available.

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