335 results on '"Pitama, Suzanne"'
Search Results
2. Māori preferences and practices in systemic health and social service collaborative practice
3. A bridge between : Te Ao Māori and Te Ara Paerangi
4. Mānawatia a Matariki!
5. Kia whakatōmuri te haere whakamua : engaging Māori rural communities in health and social service care
6. Te manu kai i te mātauranga : indigenous psychology in Aotearoa/New Zealand
7. Exploring elderly Maori experiences of aged residential care using a kaupapa Maori research paradigm: Methodological considerations
8. ‘People that suffer or have been through it know the answers’: stakeholders’ perspectives on improving healthcare systems for end-of-life care in chronic obstructive pulmonary disease
9. Reimagining eating disorder spaces: a qualitative study exploring Māori experiences of accessing treatment for eating disorders in Aotearoa New Zealand
10. Sustained excellence
11. Sudden unexpected death in infancy (SUDI) in New Zealand : discussion over the last 5 years and where to from here?
12. Institutional pathways to psychosis for Indigenous Māori: A qualitative exploration of experiences
13. Interviews with Indigenous Māori with type 1 diabetes using open-source automated insulin delivery in the CREATE randomised trial
14. Improving Māori health through clinical assessment : Waikare o te Waka o Meihana
15. Exploring Maori health worker perspectives on colorectal screening
16. Adjusting protocols in clinical research : finding the point of cultural/clinical fusion
17. Coping with earthquake trauma
18. The value of te reo in primary care
19. Cultural biases in the Peabody Picture Vocabulary Test-III : testing tamariki in a New Zealand sample
20. Meihana model : a clinical assessment framework
21. Maori experiences of hospital care: A qualitative systematic review
22. Indigenous peoples' experiences and preferences in aged residential care: A systematic review
23. A Systematic Review of Bipolar Disorder in Indigenous Peoples
24. Exploring indigenous ethnic inequities in first episode psychosis in New Zealand – A national cohort study
25. The Right to Equal Health: Best Practice Priorities for Māori with Bipolar Disorder from Staff Focus Groups.
26. 'E koekoe te Tūī, e ketekete te Kākā, e kuku te Kererū, The Tūī chatters, the Kākā cackles, and the Kererū coos': Insights into explanatory factors, treatment experiences and recovery for Māori with eating disorders – A qualitative study
27. It's not special treatment... That's part of the Treaty of Waitangi! Organisational barriers to enhancing the Aged Residential Care environment for older Māori and Whānau in New Zealand.
28. Reported sources of health inequities in Indigenous Peoples with chronic kidney disease: a systematic review of quantitative studies
29. ‘It’s about having that knowledge, tino rangatiratanga!’ Understanding structural barriers to accessing aged residential care services among older Māori in New Zealand
30. It's not special treatment… That's part of the Treaty of Waitangi! Organisational barriers to enhancing the Aged Residential Care environment for older Māori and Whānau in New Zealand
31. ‘E koekoe te Tūī, e ketekete te Kākā, e kuku te Kererū, The Tūī chatters, the Kākā cackles, and the Kererū coos’: Insights into explanatory factors, treatment experiences and recovery for Māori with eating disorders – A qualitative study
32. A bridge between: Te Ao Māori and Te Ara Paerangi
33. Racism, early psychosis, and institutional contact: A qualitative study of Indigenous experiences
34. Acute aortic syndrome: nationwide study of epidemiology, management, and outcomes
35. Professional development: The impacts of being a 'roadshow facilitator' on Indigenous health tertiary students
36. Race and racism: Keynote presentation: Externalising a complicated situation - Teaching racism in an indigenous curriculum: A case study
37. Survival Disparity Following Abdominal Aortic Aneurysm Repair Highlights Inequality in Ethnic and Socio-economic Status
38. Policy, system and service design influence on healthcare inequities for people with end-of-life chronic obstructive airways disease, their support people and health professionals.
39. ‘People that suffer or have been through it know the answers’: Stakeholders’ perspectives on improving healthcare systems for end-of-life care in chronic obstructive airways disease
40. Reported Māori consumer experiences of health systems and programs in qualitative research: a systematic review with meta-synthesis
41. Positioning Stakeholder Perspectives in COPD End-of-Life Care Using Critical Theory and Actor-Network Theory: A Methodological Approach.
42. Enzyme replacement in advanced pancreatic cancer: patient perceptions.
43. Acute aortic syndrome: nationwide study of epidemiology, management, and outcomes.
44. A proposed hauora Maori clinical guide for psychologists: Using the hui process and Meihana model in clinical assessment and formulation
45. Stakeholders’ Perspectives on the Quality of End-of-Life Health Care Services for Chronic Obstructive Airways Disease: A Focus Group Study
46. On pandemics and pivots: a COVID-19 reflection on envisioning the future of medical education
47. Educating for Indigenous Health Equity: An International Consensus Statement
48. Consolidated criteria for strengthening reporting of health research involving indigenous peoples: the CONSIDER statement
49. Informed consent for medical student involvement in patient care: an updated consensus statement.
50. Non-Indigenous privilege in health, justice and social services preceding first episode psychosis: A population-based cohort study.
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