Items where authors include "Taylor, R.W."

Article

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Dudgeon, A.P. orcid.org/0000-0002-4536-1147 et al. (9 more authors) (2024) Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology. The Analyst, 149 (9). pp. 2738-2746. ISSN 0003-2654

Jebeile, H., Lister, N.B., Libesman, S. et al. (64 more authors) (2023) Eating disorders in weight-related therapy (EDIT): Protocol for a systematic review with individual participant data meta-analysis of eating disorder risk in behavioural weight management. PLOS ONE, 18 (7). e0282401. ISSN 1932-6203

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Schooling, C.N. et al. (9 more authors) (2023) Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue. Journal of Raman Spectroscopy, 54 (3). pp. 258-268. ISSN 0377-0486

Nolden, K.A., Egner, J.M., Collier, J.J. et al. (21 more authors) (2022) Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms. Life Science Alliance, 5 (12). ARTN e202101284.

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Lloyd, G.R. et al. (7 more authors) (2022) The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease : a preliminary comparison between fibre optic probe and microscope formats. Journal of Raman Spectroscopy, 53 (2). pp. 172-181. ISSN 0377-0486

Zierz, C.M., Baty, K., Blakely, E.L. et al. (7 more authors) (2019) A novel pathogenic variant in MT-CO2 causes an isolated mitochondrial complex IV deficiency and late-onset cerebellar ataxia. Journal of Clinical Medicine, 8 (6). 789. ISSN 2077-0383

Ng, Y.S., Powell, H., Hoggard, N. orcid.org/0000-0002-6447-7639 et al. (3 more authors) (2017) Novel POLG variants associated with late-onset de novo status epilepticus and progressive ataxia. Neurology Genetics, 3 (5). e181. ISSN 2376-7839

Dombi, E., Diot, A., Morten, K. et al. (16 more authors) (2016) The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. Neurology, 86 (20). pp. 1921-1923. ISSN 0028-3878

Bargiela, D., Shanmugarajah, P., Lo, C. et al. (6 more authors) (2015) Mitochondrial pathology in progressive cerebellar ataxia. Cerebellum & Ataxias, 2. 16.