Design and rationale of the tobacco, exercise and diet messages (TEXT ME) trial of a text message-based intervention for ongoing prevention of cardiovascular disease in people with...

por Chow, C K, Redfern, J, Thiagalingam, A, Jan, S, Whittaker, R, Hackett, M, Graves, N, Mooney, J, Hillis, G S
Publicado 2012

Whānau Māori and Pacific peoples’ knowledge, perceptions, expectations and solutions regarding antibiotic treatment of upper respiratory tract infections: a qualitative study

por Thaggard, S, Reid, S, Chan, AHY, White, C, Fraser, L, Arroll, BA, Best, E, Whittaker, R, Wells, S, Thomas, MG, Ritchie, SR
Publicado 2023

An example of governance for AI in health services from Aotearoa New Zealand

por Whittaker, R., Dobson, R., Jin, C. K., Style, R., Jayathissa, P., Hiini, K., Ross, K., Kawamura, K., Muir, P.
Publicado 2023

Long‐term follow‐up of a randomized controlled trial of a text‐message diabetes self‐management support programme, SMS4BG

por Dobson, R., Whittaker, R., Jiang, Y., McNamara, C., Shepherd, M., Maddison, R., Cutfield, R., Khanolkar, M., Murphy, R.
Publicado 2019

Validation of primary metal-on-metal hip arthroplasties on the National Joint Registry for England, Wales and Northern Ireland using data from the London Implant Retrieval Centre:...

por Sabah, S. A., Henckel, J., Cook, E., Whittaker, R., Hothi, H., Pappas, Y., Blunn, G., Skinner, J. A., Hart, A. J.
Publicado 2015

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

Evaluation of swabbing methods for estimating the prevalence of bacterial carriage in the upper respiratory tract: a cross sectional study

por Coughtrie, A L, Whittaker, R N, Begum, N, Anderson, R, Tuck, A, Faust, S N, Jefferies, J M, Yuen, H M, Roderick, P J, Mullee, M A, Moore, M V, Clarke, S C
Publicado 2014

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

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