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Journal of Health Services Research & Policy|August 2, 2005
When is research on patient records without consent ethical?Michael Parker
Psychological Medicine|April 29, 2005
Beyond major depressionGordon Parker
Social Science & Medicine (1982)|August 1, 1993
Bilharzia and the boys: questioning common assumptionsM Parker
AJOB Neuroscience|July 17, 2025
The Memory Remains: Reciprocity and Veteran Super SoldiersParker Crutchfield
Monash Bioethics Review|October 13, 2025
Moral craft: engaging with value pluralism in healthcare decision-makingMichael Parker
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)|April 10, 2013
The history and development of Australia's Black Dog InstituteGordon Parker
Journal of Medical Ethics|March 1, 1990
Moral intuition, good deaths and ordinary medical practitionersM Parker
International Journal of Law and Psychiatry|July 13, 2013
Defending the indefensible? Psychiatry, assisted suicide and human freedomMalcolm Parker
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
The pooling of manpower and resources through the establishment of European reference networks and rare disease patient registries is a necessary area of collaboration for rare renal disordersSamantha Parker
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