Adherence to hunger training using blood glucose monitoring: a feasibility study

por Jospe, M. R., Brown, R. C., Roy, M., Taylor, R. W.
Publicado 2015

Diquat causes caspase-independent cell death in SH-SY5Y cells by production of ROS independently of mitochondria

por Nisar, R., Hanson, P. S., He, L., Taylor, R. W., Blain, P. G., Morris, C. M.
Publicado 2015

Erratum to: Diquat causes caspase-independent cell death in SH-SY5Y cells by production of ROS independently of mitochondria

por Nisar, R., Hanson, P. S., He, L., Taylor, R. W., Blain, P. G., Morris, C. M.
Publicado 2015

Self‐monitoring has no adverse effect on disordered eating in adults seeking treatment for obesity

por Jospe, M. R., Brown, R. C., Williams, S. M., Roy, M., Meredith‐Jones, K. A., Taylor, R. W.
Publicado 2018

Mitochondrial DNA deletions and depletion within paraspinal muscles

por Campbell, G R, Reeve, A, Ziabreva, I, Polvikoski, T M, Taylor, R W, Reynolds, R, Turnbull, D M, Mahad, D J
Publicado 2013

Organic matter composition and thermal stability influence greenhouse gases production in subtropical peatland under different vegetation types

por Akinbi, G.O., Ngatia, L.W., Grace, J.M., Fu, R., Tan, C., Olaborode, S.O., Abichou, T., Taylor, R.W.
Publicado 2022

Improving rates of overweight, obesity and extreme obesity in New Zealand 4‐year‐old children in 2010–2016

por Shackleton, N., Milne, B. J., Audas, R., Derraik, J. G. B., Zhu, T., Taylor, R. W., Morton, S. M. B., Glover, M., Cutfield, W. S., Taylor, B.
Publicado 2017

Initial development and validation of a mitochondrial disease quality of life scale

por Elson, J.L., Cadogan, M., Apabhai, S., Whittaker, R.G., Phillips, A., Trennell, M.I., Horvath, R., Taylor, R.W., McFarland, R., McColl, E., Turnbull, D.M., Gorman, G.S.
Publicado 2013

Biallelic mutations in mitochondrial tryptophanyl‐tRNA synthetase cause Levodopa‐responsive infantile‐onset Parkinsonism

por Burke, E.A., Frucht, S.J., Thompson, K., Wolfe, L.A., Yokoyama, T., Bertoni, M., Huang, Y., Sincan, M., Adams, D.R., Taylor, R.W., Gahl, W.A., Toro, C., Malicdan, M.C.V.
Publicado 2018

Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease

por Boczonadi, V., King, M. S., Smith, A. C., Olahova, M., Bansagi, B., Roos, A., Eyassu, F., Borchers, C., Ramesh, V., Lochmüller, H., Polvikoski, T., Whittaker, R. G., Pyle, A., Griffin, H., Taylor, R. W., Chinnery, P. F., Robinson, A. J., Kunji, E. R. S., Horvath, R.
Publicado 2019

A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disorders

por Rodenburg, R.J.T., Schoonderwoerd, G.C., Tiranti, V., Taylor, R.W., Rötig, A., Valente, L., Invernizzi, F., Chretien, D., He, L., Backx, G.P.B.M., Janssen, K.J.G.M., Chinnery, P.F., Smeets, H.J., de Coo, I.F., van den Heuvel, L.P.
Publicado 2013

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

por Yu-Wai-Man, P., Griffiths, P.G., Gorman, G.S., Lourenco, C.M., Wright, A.F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M.L., Caporali, L., Lamperti, C., Tallaksen, C.M., Duffey, P., Miller, J., Whittaker, R.G., Baker, M.R., Jackson, M.J., Clarke, M.P., Dhillon, B., Czermin, B., Stewart, J.D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R.W., Turnbull, D.M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L.A., Horvath, R., Amati-Bonneau, P., Chinnery, P.F.
Publicado 2010