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Louise Locock

Showing results (1-10 of 125) with videos related to

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Journal of Health Services Research & Policy|June 25, 2003
Redesigning health care: new wine from old bottles?Louise Locock
The Veterinary Record|November 12, 2017
Labour and love for Mr PinkLouise Locock
The 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 Kai
Clinical Trials (London, England)|December 18, 2010
Personal benefit, or benefiting others? Deciding whether to take part in clinical trialsLouise Locock, Lorraine Smith
Social Science & Medicine (1982)|September 17, 2005
'Just a bystander'? Men's place in the process of fetal screening and diagnosisLouise Locock, Jo Alexander
Patient Education and Counseling|July 9, 2011
Personal experiences of taking part in clinical trials - a qualitative studyLouise Locock, Lorraine Smith
Nature|September 14, 2013
Health care: Bring on the evidenceSophie Petit-Zeman, Louise Locock
Social 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 Brown
Health 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 Boylan
Chronic Illness|March 30, 2012
Metaphoric language and the articulation of emotions by people affected by motor neurone diseaseLouise Locock, Fadhila Mazanderani, John Powell
Pageof 13

Showing results (1-10 of 125) with videos related to

Sort By:
Pageof 13
Journal of Health Services Research & Policy|June 25, 2003
Redesigning health care: new wine from old bottles?Louise Locock
The Veterinary Record|November 12, 2017
Labour and love for Mr PinkLouise Locock
The 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 Kai
Clinical Trials (London, England)|December 18, 2010
Personal benefit, or benefiting others? Deciding whether to take part in clinical trialsLouise Locock, Lorraine Smith
Social Science & Medicine (1982)|September 17, 2005
'Just a bystander'? Men's place in the process of fetal screening and diagnosisLouise Locock, Jo Alexander
Patient Education and Counseling|July 9, 2011
Personal experiences of taking part in clinical trials - a qualitative studyLouise Locock, Lorraine Smith
Nature|September 14, 2013
Health care: Bring on the evidenceSophie Petit-Zeman, Louise Locock
Social 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 Brown
Health 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 Boylan
Chronic Illness|March 30, 2012
Metaphoric language and the articulation of emotions by people affected by motor neurone diseaseLouise Locock, Fadhila Mazanderani, John Powell
Pageof 13