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- ...<ref>[http://www.npcf.nl/ NPCF] (2008), "Gids Patiënteninformatie 2008" (''Patient information guide'')</ref> ...#1, 2006, 9-14</ref> scientific research, and together with other patient organizations represented patients in the development of protocols and guidelines.<ref na ...7 KB (929 words) - 21:32, 2 October 2014
- ...=EMEA|website=www.euro-me.org|access-date=2019-09-18}}</ref> It has member organizations from Belgium, Denmark, Germany, Ireland, Italy, Netherlands, Norway, Spain, ==Member organizations== ...1 KB (175 words) - 01:09, 18 September 2019
- ...16321154</ref> The RNase L fragmentation has been shown to correlate with patient dysfunction and to be useful as a [[marker (medicine)|marker]] for ME.<ref> ...08] (''"Care for ME/CFS patients. Experiences of the supporters of patient organizations with health care."'')</ref> Coping techniques for ME invariably include som ...16 KB (2,313 words) - 01:18, 31 December 2011
- * Doorlopende Enquête Patiëntenperspectief (''Continuous Patient Perspective Survey'')<ref>G. den Broeder (2015), [http://www.meresearch.nl/ ...part of the 'Hersenstraat' (''Brain Street''), a joint activity by member organizations of the Dutch Brain Council to present themselves at events.<ref>PGO Support ...7 KB (831 words) - 22:08, 17 September 2019
- ...' (Science for Patients) is the title of several projects of Dutch patient organizations, including the [[ME Vereniging Nederland]] and the [[ME/cvs Vereniging]]. I ...1 KB (188 words) - 22:37, 17 September 2019