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125 results on '"Miller, Fiona A."'

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1. Planning for social justice, anticipating sea level rise: the case of Lake Macquarie, Australia.

2. Transgenerational Trauma and Trust Restoration.

3. Rescaling political ecology? World regional approaches to climate change in the Asia Pacific.

4. Exploring the consequences of climate-related displacement for just resilience in Vietnam.

5. Slow, small and shared voluntary relocations: Learning from the experience of migrants living on the urban fringes of Khulna, Bangladesh.

6. Climate‐related displacement in the Asia Pacific: Justice, rights and culture.

7. Resettlement and the environment in Vietnam: Implications for climate change adaptation planning.

8. Genetic counselors' preferences for coverage of preimplantation genetic diagnosis: A discrete choice experiment.

9. The institutional workers of biomedical science: Legitimizing academic entrepreneurship and obscuring conflicts of interest.

10. False-Positive Newborn Screening for Cystic Fibrosis and Health Care Use.

11. Heat as emergency, heat as chronic stress: policy and institutional responses to vulnerability to extreme heat.

12. Understanding relevance of health research: considerations in the context of research impact assessment.

13. How do Policy and Institutional Settings Shape Opportunities for Community-Based Primary Health Care? A Comparison of Ontario, Québec and New Zealand.

14. Health Canada needs to act on laboratory-developed diagnostics.

15. Parent Experience With False-Positive Newborn Screening Results for Cystic Fibrosis.

16. Resources and population served: a description of the Ontario Paediatric Diabetes Network.

17. Citizen expectations of 'academic entrepreneurship' in health research: public science, practical benefit.

18. Expectations and values about expanded newborn screening: a public engagement study.

19. The relevance of a coproductive capacity framework to climate change adaptation: investigating the health and water sectors in Cambodia.

20. Public views on participating in newborn screening using genome sequencing.

21. The Effervescent Patriot: Jean-Jacques Rousseau on Achieving One’s Country.

23. The Consultant's intermediary role in the regulation of molecular diagnostics in the US.

24. What We Should Learn from Rousseau’s Portrayal of Women or Humiliation as Social Integration.

25. Saving Grace: The Incarnational Art of Flannery OConnor, the "Bad Catholicism" of Walker Percy and the Immanent Mysticism of Nietzsche as Potential Routes to the Quickening of Bourgeois Liberalism.

26. The Political Virtue of Hypocrisy: A Nietzschean Critique of Rousseauan Sincerity (with a Rousseauan Rebuttal).

27. Analyzing The Pace and Direction of Primary Health Care Reform in Ontario, Canada: Transformative Change or Tranformation Lite?

28. Constructing Risk: multi-scale change, livelihoods and vulnerability in the Mekong Delta, Vietnam.

29. Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care.

30. A Plan to Push Limits? Investigating the ecologically sustainable development dimensions of Melbourne's Central Region sustainable water strategy.

31. Questioning the assumptions: the role of vulnerability assessments in climate change adaptation.

32. The Sad Story of Newborn Screening for Krabbe: The Need for Good Governance.

33. Antibias Efforts in United States Maternity Care: A Scoping Review of the Publicly Funded Health Equity Intervention Pipeline.

34. Leveraging the “living laboratory”: On the emergence of the entrepreneurial hospital.

35. Leveraging the “living laboratory”: On the emergence of the entrepreneurial hospital

36. One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants.

37. Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

38. Citizens' Values Regarding Research With Stored Samples From Newborn Screening in Canada.

39. What does 'respect for persons' require? Attitudes and reported practices of genetics researchers in informing research participants about research.

40. Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results.

41. Reframing norms: boundary maintenance and partial accommodations in the work of academic technology transfer.

42. The primary care physician role in cancer genetics: a qualitative study of patient experience.

43. Resilience and Vulnerability: Complementary or Conflicting Concepts?

44. What is a meaningful result? Disclosing the results of genomic research in autism to research participants.

45. Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

46. Understanding sickle cell carrier status identified through newborn screening: a qualitative study.

47. Informing Parents About Expanded Newborn Screening: Influences on Provider Involvement.

48. Imagining value, imagining users: Academic technology transfer for health innovation

49. Contending visions in the evolution of genetic medicine: The case of cancer genetic services in Ontario, Canada

50. Testicular calcification and microlithiasis: association with primary intra-testicular malignancy in 3,477 patients.

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