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Disability and Rehabilitation|June 23, 2018
Myalgic encephalomyelitis/chronic fatigue syndrome and the biopsychosocial model: a review of patient harm and distress in the medical encounterKeith J Geraghty, Charlotte BleaseJournal of Health Psychology|September 17, 2016
Cognitive behavioural therapy in the treatment of chronic fatigue syndrome: A narrative review on efficacy and informed consentKeith J Geraghty, Charlotte BleaseJournal of Bioethical Inquiry|July 5, 2018
Are ME/CFS Patient Organizations "Militant"? : Patient Protest in a Medical ControversyCharlotte Blease, Keith J GeraghtyJournal of Health Psychology|March 28, 2022
Long Covid at the crossroads: Comparisons and lessons from the treatment of patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)Joanne Hunt, Charlotte Blease, Keith J GeraghtyJournal of Medical Ethics|April 30, 2013
The duty to be well-informed: the case of depressionCharlotte BleasePerspectives in Biology and Medicine|October 9, 2018
Consensus in Placebo Studies: Lessons from The Philosophy of ScienceCharlotte BleaseMedical Humanities|February 5, 2016
In defence of utility: the medical humanities and medical educationCharlotte BleaseJournal of Medical Ethics|December 5, 2023
Open AI meets open notes: surveillance capitalism, patient privacy and online record accessCharlotte BleaseJournal of Medical Ethics|October 22, 2010
Deception as treatment: the case of depressionCharlotte BleaseJournal of Medical Ethics|November 4, 2011
The principle of parity: the 'placebo effect' and physician communicationCharlotte BleasePageof 12