Evidence-based activism: Patients’, users’ and activists’ groups in knowledge society
暂无分享,去创建一个
Tiago Moreira | M. Akrich | V. Rabeharisoa | Vololona Rabeharisoa | Tiago Moreira | Madeleine Akrich
[1] M. Langer. The illness experience , 2014, Canadian Medical Association Journal.
[2] E. Howlett,et al. Tracking Transformations in Health Movement Organisations: Alzheimer's Disease Organisations and their Changing ‘Cause Regimes’ , 2013 .
[3] I. Stengers,et al. The cosmopolitical proposal , 2013 .
[4] Tiago Moreira. Health Care Standards and the Politics of Singularities , 2012 .
[5] N. Tomes,et al. Patients as Policy Actors , 2013 .
[6] S. Epstein. Measuring success scientific, institutional, and cultural effects of patient advocacy , 2011 .
[7] C. Silverman. Understanding Autism: Parents, Doctors, and the History of a Disorder , 2011 .
[8] K. Barker. Listening to Lyrica: contested illnesses and pharmaceutical determinism. , 2011, Social science & medicine.
[9] Brice Laurent,et al. Technologies of Democracy: Experiments and Demonstrations , 2011, Sci. Eng. Ethics.
[10] H. Lofgren,et al. Democratizing Health: Consumer Groups in the Policy Process , 2011 .
[11] A. Faulkner. The Artificial Ear: Cochlear Implants and the Culture of Deafness , 2011 .
[12] M. Davis. Biomedicalization: technoscience, health, and illness in the US , 2011 .
[13] Aaron Panofsky. Generating sociability to drive science: Patient advocacy organizations and genetics research , 2011, Social studies of science.
[14] Michaela Mueller. Acting in An Uncertain World: An Essay on Technical Democracy , 2011 .
[15] Tiago Moreira,et al. Medical proofs, social experiments : clinical trials in shifting contexts , 2010 .
[16] Gwen Ottinger,et al. Undone Science: Charting Social Movement and Civil Society Challenges to Research Agenda Setting , 2010, Science, technology & human values.
[17] D. Hess. The Potentials and Limitations of Civil Society Research: Getting Undone Science Done , 2009 .
[18] 하대청. Acting in an Uncertain World , 2009 .
[19] A. Clarke,et al. Biomedicalization : technoscience, health, and illness in the U.S. , 2009 .
[20] Michel Callon,et al. Acting in an uncertain world , 2009 .
[21] A. Fearnley. Inclusion: The Politics of Difference in Medical Research , 2008 .
[22] Steven Epstein,et al. Patient Groups and Health Movements , 2008 .
[23] Peter Conrad,et al. The Medicalization of Society: On the Transformation of Human Conditions into Treatable Disorders , 2007 .
[24] C. Novas. The Political Economy of Hope: Patients’ Organizations, Science and Biovalue , 2006 .
[25] Alberto Cambrosio,et al. Regulatory objectivity and the generation and management of evidence in medicine. , 2006, Social science & medicine.
[26] S. Philpin. The Fibromyalgia Story: Medical Authority and Women's Worlds of Pain ‐ by Barker, K.K. , 2006 .
[27] D. Longo. Speaking for patients and carers: health consumer groups and the policy process , 2006 .
[28] K. Landzelius. Introduction: Patient organization movements and new metamorphoses in patienthood. , 2006, Social science & medicine.
[29] V. Rabeharisoa,et al. From representation to mediation: the shaping of collective mobilization on muscular dystrophy in France. , 2006, Social science & medicine.
[30] J. Dumit. Illnesses you have to fight to get: facts as forces in uncertain, emergent illnesses. , 2006, Social science & medicine.
[31] Janine Barbot,et al. How to build an "active" patient? The work of AIDS associations in France. , 2006, Social science & medicine.
[32] R. J. Evenson. The Fibromyalgia Story: Medical Authority and Women's Worlds of Pain (review) , 2005 .
[33] B. Latour,et al. Making Things Public : Atmospheres of Democracy , 2005 .
[34] J. Allsop,et al. Speaking for Patients and Carers: Health Consumer Groups and the Policy Process , 2004 .
[35] J. Allsop,et al. Health consumer groups in the UK: a new social movement? , 2004, Sociology of health & illness.
[36] P. Brown,et al. Social movements in health: an introduction. , 2004, Sociology of health & illness.
[37] A. Rosoff. THE GOLD STANDARD: THE CHALLENGE OF EVIDENCE-BASED MEDICINE AND STANDARDIZATION IN HEALTH CARE , 2004 .
[38] S. Jasanoff. States of Knowledge: The Co-production of Science and the Social Order , 2004 .
[39] Jean Gayton Carroll,et al. The Gold Standard: The Challenge of Evidence-Based Medicine and Standardization in Health Care , 2004 .
[40] M. Callon,et al. Patients and scientists in French muscular dystrophy research , 2004 .
[41] Phil Brown,et al. Embodied health movements: new approaches to social movements in health. , 2004, Sociology of health & illness.
[42] Alberto Cambrosio,et al. Biomedical Platforms: Realigning the Normal and the Pathological in Late-Twentieth-Century Medicine , 2003 .
[43] Janine Pierret,et al. The illness experience: state of knowledge and perspectives for research. , 2003, Sociology of health & illness.
[44] N. Dodier,et al. Leçons politiques de l'épidémie de sida , 2003 .
[45] Rohit Parikh,et al. States of Knowledge , 2002, WoLLIC.
[46] Nicolas Dodier,et al. Multiplicity in Scientific Medicine: The Experience of HIV-Positive Patients , 2002 .
[47] S. Franklin,et al. Relative Values : Reconfiguring Kinship Studies , 2017 .
[48] J. Barbot. Les malades en mouvements : la médecine et la science à l'épreuve du sida , 2002 .
[49] Stephanie J. Bird,et al. Science and Engineering Ethics , 2000 .
[50] Mary-Jo DelVecchio Good,et al. Differences in Medicine: Unraveling Practices, Techniques, and Bodies , 1999 .
[51] Marc Berg,et al. Differences in Medicine: Unraveling Practices, Techniques, and Bodies , 1999 .
[52] Peter Galison,et al. The science studies reader , 1999 .
[53] S. Epstein. Impure Science: AIDS, Activism, and the Politics of Knowledge , 1998, Nature Medicine.
[54] A. Stockdale. Conflicting perspectives : coping with cystic fibrosis in the age of molecular medicine , 1997 .
[55] Sheila Jasanoff,et al. Handbook of Science and Technology Studies , 1995 .
[56] Steven Epstein,et al. The Construction of Lay Expertise: AIDS Activism and the Forging of Credibility in the Reform of Clinical Trials , 1995, Science, technology & human values.
[57] A. Mol,et al. Regions, Networks and Fluids: Anaemia and Social Topology , 1994, Social studies of science.
[58] H. Arksey. Expert and lay participation in the construction of medical knowledge , 1994 .
[59] P. Haas. Introduction: epistemic communities and international policy coordination , 1992, International Organization.
[60] Peter Conrad,et al. Medicalization and Social Control , 1992 .
[61] D W Light,et al. Professionalism as a countervailing power. , 1991, Journal of health politics, policy and law.
[62] Anselm L. Strauss,et al. Unending work and care: Managing chronic illness at home. , 1989 .
[63] B. Latour,et al. Power, Action and Belief. A New Sociology of Knowledge? , 1986 .
[64] M. Callon. Some Elements of a Sociology of Translation: Domestication of the Scallops and the Fishermen of St Brieuc Bay , 1984 .
[65] T. Borkman. Experiential Knowledge: A New Concept for the Analysis of Self-Help Groups , 1976, Social Service Review.