Zobrazeno 1 - 10
of 897
pro vyhledávání: '"Davies SJ"'
Publikováno v:
Journal of Pain Research, Vol Volume 10, Pp 2089-2095 (2017)
Gregory F Parkin-Smith,1,2 Stephanie J Davies,3–5 Lyndon G Amorin-Woods2,61General Practice, Dunsborough WA, Australia; 2School of Health Professions, Murdoch University, Perth, WA, Australia; 3Private Practice Pain Medicine, Painless Clinic, Perth
Externí odkaz:
https://doaj.org/article/d8e5f390192547ee9abf5bc45fcbfab9
Publikováno v:
Journal of Pain Research, Vol 2015, Iss default, Pp 741-752 (2015)
Gregory F Parkin-Smith,1 Lyndon G Amorin-Woods,2–4 Stephanie J Davies,5–7 Barrett E Losco,8 Jon Adams9,10 1General Practice, Surgery 82, Busselton, WA, Australia; 2School of Health Professions, Murdoch University, Murdoch, WA, Australia; 3Chiropr
Externí odkaz:
https://doaj.org/article/bab204018ec6461293ab7b9ab703bf71
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol 2011, Iss Issue 1, Pp 431-439 (2011)
David M Christmas, JP Potokar, Simon JC DaviesAcademic Unit of Psychiatry, School of Social and Community Medicine, University of Bristol, Bristol, UK A presentation relating to this manuscript was made by Dr David Christmas at the 9th International
Externí odkaz:
https://doaj.org/article/051bdd674e7b4926b2909d702f9fc307
Autor:
Davies, SJ, Zhao, J, McCullough, KP, Kim, Y-L, Wang, AY-M, Badve, SV, Mehrotra, R, Kanjanabuch, T, Kawanishi, H, Robinson, BM, Pisoni, R, Perl, J
Publikováno v:
Kidney360. 3:872-882
Background: Icodextrin has been shown in randomized controlled trials to benefit fluid management in peritoneal dialysis (PD). We describe international icodextrin prescription practices and their relationship to clinical outcomes. Methods We analyze
Autor:
Davies, SJ, Zhao, J, Morgenstern, H, Zee, J, Bieber, B, Fuller, DS, Sloand, JA, Vychytil, A, Kawanishi, H, Johnson, DW, Wang, AY-M, Kanjanabuch, T, Boongird, S, Moraes, TP, Badve, SV, Pisoni, RL, Perl, J, Prescip, PDOPPSD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::b51d7e4a7c54346bf33741ebc262f122
https://eprints.keele.ac.uk/10399/1/PIIS2468024921010196.pdf
https://eprints.keele.ac.uk/10399/1/PIIS2468024921010196.pdf
Autor:
Koven, CD, Knox, RG, Fisher, RA, Chambers, JQ, Christoffersen, BO, Davies, SJ, Detto, M, Dietze, MC, Faybishenko, B, Holm, J, Huang, M, Kovenock, M, Kueppers, LM, Lemieux, G, Massoud, E, McDowell, NG, Muller-Landau, HC, Needham, JF, Norby, RJ, Powell, T, Rogers, A, Serbin, SP, Shuman, JK, Swann, ALS, Varadharajan, C, Walker, AP, Joseph Wright, S, Xu, C
Publikováno v:
Biogeosciences, vol 17, iss 11
Plant functional traits determine vegetation responses to environmental variation, but variation in trait values is large, even within a single site. Likewise, uncertainty in how these traits map to Earth system feedbacks is large. We use a vegetatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e7ff8e4826dca4d685f39da079becf33
https://escholarship.org/uc/item/6458741n
https://escholarship.org/uc/item/6458741n
Biocompatible solutions and long-term changes in peritoneal solute transport (vol 13, pg 1526, 2018)
Autor:
Elphick, EH, Teece, L, Chess, JA, Do, J-Y, Kim, Y-L, Lee, HB, Davison, SN, Topley, N, Davies, SJ, Lambie, MR
Background and objectives: The inflammation-driven increase in peritoneal solute transport rate that occurs during long-term peritoneal dialysis is associated with higher mortality, hospitalization, and encapsulating peritoneal sclerosis. Because bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::8885fe1cc2dff46a4dce3d058d460c86
https://eprints.keele.ac.uk/8961/1/Biocompatible-Global-Paper-290618-Archive.docx
https://eprints.keele.ac.uk/8961/1/Biocompatible-Global-Paper-290618-Archive.docx
Autor:
Qie, L, Lewis, SL, Sullivan, MJP, Lopez-Gonzalez, G, Pickavance, GC, Sunderland, T, Ashton, P, Hubau, W, Abu Salim, K, Aiba, S-I, Banin, LF, Berry, N, Brearley, FQ, Burslem, DFRP, Dančák, M, Davies, SJ, Fredriksson, G, Hamer, KC, Hédl, R, Kho, LK, Kitayama, K, Krisnawati, H, Lhota, S, Malhi, Y, Maycock, C, Metali, F, Mirmanto, E, Nagy, L, Nilus, R, Ong, R, Pendry, CA, Poulsen, AD, Primack, RB, Rutishauser, E, Samsoedin, I, Saragih, B, Sist, P, Slik, JWF, Sukri, RS, Svátek, M, Tan, S, Tjoa, A, van Nieuwstadt, M, Vernimmen, RRE, Yassir, I, Kidd, PS, Fitriadi, M, Ideris, NKH, Serudin, RM, Abdullah Lim, LS, Saparudin, MS, Phillips, OL
Publikováno v:
NATURE COMMUNICATIONS
Nature Communications
Nature Communications
© 2017 The Author(s). Less than half of anthropogenic carbon dioxide emissions remain in the atmosphere. While carbon balance models imply large carbon uptake in tropical forests, direct on-the-ground observations are still lacking in Southeast Asia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4c7802cc4f5a2397240b8509592de08c
https://hdl.handle.net/1854/LU-8677006
https://hdl.handle.net/1854/LU-8677006
Heimler syndrome is caused by hypomorphic mutations in the peroxisome-biogenesis genes PEX1 and PEX6
Autor:
Ratbi, I, Falkenberg, KD, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, JE, Chandler, KE, Williams, SJ, Roberts, NA, El Alloussi, M, Black, GC, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S, Cooper, N, Ong, KR, Smith, CEL, Inglehearn, CF, Mighell, AJ, Elcock, C, Poulter, JA, Tischkowitz, M, Davies, SJ, Sefiani, A, Mironov, AA, Newman, WG, Waterham, HR, Van Camp, G
Publikováno v:
The American journal of human genetics
Ratbi, I, Falkenberg, K D, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, J, Chandler, K E, Williams, S, Roberts, N, El Alloussi, M, Black, G, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S-A, Cooper, N, Ong, K R, Smith, C E L, Inglehearn, C F, Mighell, A J, Elcock, C, Poulter, J A, Tischkowitz, M, Davies, S J, Sefiani, A, Mironov, A, Newman, W, Waterham, H R & Van Camp, G 2015, ' Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. ', American Journal of Human Genetics, vol. 97, no. 4, pp. 535-545 . https://doi.org/10.1016/j.ajhg.2015.08.011
American journal of human genetics, 97(4), 535-545. Cell Press
Ratbi, I, Falkenberg, K D, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, J, Chandler, K E, Williams, S, Roberts, N, El Alloussi, M, Black, G, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S-A, Cooper, N, Ong, K R, Smith, C E L, Inglehearn, C F, Mighell, A J, Elcock, C, Poulter, J A, Tischkowitz, M, Davies, S J, Sefiani, A, Mironov, A, Newman, W, Waterham, H R & Van Camp, G 2015, ' Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. ', American Journal of Human Genetics, vol. 97, no. 4, pp. 535-545 . https://doi.org/10.1016/j.ajhg.2015.08.011
American journal of human genetics, 97(4), 535-545. Cell Press
Heimler syndrome (HS) is a rare recessive disorder characterized by sensorineural hearing loss (SNHL), amelogenesis imperfecta, nail abnormalities and occasional or late onset retinal pigmentation. We ascertained eight families with HS, and - using a