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International Journal of Pediatric Otorhinolaryngology|December 21, 2012
Patients/carers and clinicians can set joint priorities for research in cleft lip and palateSophie Petit-Zeman, Katherine CowanThe Journal of Ambulatory Care Management|June 12, 2010
"Natural ground" for medical research charities: public and patient involvement in research fundingSophie Petit-Zeman, Elizabeth Philpots, Simon DenegriJournal of Health Services Research & Policy|June 25, 2003
Redesigning health care: new wine from old bottles?Louise LocockThe British Journal of General Practice : the Journal of the Royal College of General Practitioners|March 6, 2008
Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics eraLouise Locock, Joe KaiClinical Trials (London, England)|December 18, 2010
Personal benefit, or benefiting others? Deciding whether to take part in clinical trialsLouise Locock, Lorraine SmithSocial Science & Medicine (1982)|September 17, 2005
'Just a bystander'? Men's place in the process of fetal screening and diagnosisLouise Locock, Jo AlexanderPatient Education and Counseling|July 9, 2011
Personal experiences of taking part in clinical trials - a qualitative studyLouise Locock, Lorraine SmithSocial Science & Medicine (1982)|August 20, 2010
'All in the same boat'? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND)Louise Locock, Janice B BrownHealth Expectations : an International Journal of Public Participation in Health Care and Health Policy|June 16, 2015
Biosamples as gifts? How participants in biobanking projects talk about donationLouise Locock, Anne-Marie R BoylanPageof 12