Full title: Perceptions of European ME/CFS Experts Concerning Knowledge and Understanding of ME/CFS among Primary Care Physicians in Europe: A Report from the European ME/CFS Research Network (EUROMENE)
Open access, https://www.mdpi.com/1010-660X/57/3/208/htm
When is lack of scientific integrity a reason for retracting a paper? A case study.
Abstract:
This editorial has just come out in the Journal of Psychosomatic Research. It is a discussion of issues that arose from this 2004 publication:
This study is a triple-blinded randomised controlled...
Full title: The Neuroinflammatory Etiopathology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
https://www.frontiersin.org/articles/10.3389/fphys.2017.00088/full
Full title:
Reduced endothelial function in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome - results from open-label cyclophosphamide intervention study
Provisionally accepted
https://www.frontiersin.org/articles/10.3389/fmed.2021.642710/abstract
Full title: Cost-effectiveness of Interventions for Chronic Fatigue Syndrome or Myalgic Encephalomyelitis: A Systematic Review of Economic Evaluations
Open access, https://link.springer.com/article/10.1007/s40258-021-00635-7
Effects of Post-Exertional Malaise on Markers of Arterial
Stiffness in Individuals with Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome
https://www.mdpi.com/1660-4601/18/5/2366/htm
Some people insist ME can only follow from an enterovirus; there are other post viral/infectious sequelae but they are distinctly different and not ME.
I don’t recall reading about any studies that showed this but I don’t know or recall every bit of evidence of course.
I imagine there is supposed to be a point somewhere in there but all I read is people saying if they had been tasked with it they would have done it differently because they don't like the outcome it gave without being there to change it to their preference. No substantial argument other than...
Sorry about the clickbait title. :)
So here is my situation and strategy: Right now I am the only person in the entire country advocating for ME/CFS, I'm literally like the Popular Front of Judea. I have a group and followers but they are very passive as it is still quite a new community. I'm...
I can't see any CFS criteria being mentioned, so I'm not sure whether the patients are well-defined CFS patients or not.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888998/
This thread has been split from a thread discussing a book about Ron Davis:
The Puzzle Solver by Tracie White
I've been following ME/CFS research and news and reading forums for over 25 years. I think that the UK has played a much bigger part internationally in psychologising the condition and...
Myalgic encephalomyelitis/chronic fatigue syndrome and gulf war illness patients exhibit increased humoral responses to the herpesviruses-encoded dUTPase: Implications in disease pathophysiology
Peter Halpin 1, Marshall Vance Williams 1 2, Nancy G Klimas 3 4, Mary Ann Fletcher 3 4, Zachary...
They talk, in the abstract, about chronic fatigue only, but the patients they discuss have gone through a "CFS/ME" assessment, so may or may not have ME.
Open access, https://www.tandfonline.com/doi/full/10.1080/01459740.2021.1883011
This part possibly explains a bit more clearly what the...
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