37 results on '"Guha, Chandana"'
Search Results
2. School attendance and sport participation amongst children with chronic kidney disease: a cross-sectional analysis from the Kids with CKD (KCAD) study
3. Consumer involvement in the development and dissemination of chronic kidney disease guidelines: a summary of a meaningful and sustainable approach developed by Caring for Australians and New ZealandeRs with kidney Impairment guidelines
4. Socioeconomic Position and Health Among Children and Adolescents With CKD Across the Life-Course
5. Baseline characteristics of participants in the NAVKIDS.sup.2 trial: a patient navigator program in children with chronic kidney disease
6. The randomized controlled trial (NAVKIDS2) of a patient navigator program created for children with chronic kidney disease
7. Improving Diverse and Equitable Involvement of Patients and Caregivers in Research in CKD: Report of a Better Evidence and Translation–Chronic Kidney Disease (BEAT-CKD) Workshop
8. Patient-Centered Research and Outcomes in Cancer and Kidney Transplantation
9. Patient-Centered Research and Innovation in Nephrology
10. Patient Perspectives on Clotting in the Extracorporeal Circuit and Decision-Making Regarding Anticoagulation Therapy
11. The Impact of the COVID-19 Pandemic on Patients With CKD: Systematic Review of Qualitative Studies
12. Sociodemographic Drivers of Donor and Recipient Gender Disparities in Living Kidney Donation in Australia
13. Patients’ Perspectives, Factors, and Patterns of eHealth Use in Kidney Transplant Recipients
14. Longitudinal assessment of the health-related quality of life of children and adolescents with chronic kidney disease
15. Perspectives on ability to work from patients’ receiving dialysis and caregivers: analysis of data from the global SONG initiative
16. NAVKIDS2 trial: a multi-centre, waitlisted randomised controlled trial of a patient navigator intervention in children with chronic kidney disease — statistical analysis plan and update to the protocol
17. Outcomes for clinical trials involving adults with chronic kidney disease: a multinational Delphi survey involving patients, caregivers and health professionals.
18. Perspectives of solid organ transplant recipients on medicine-taking: Systematic review of qualitative studies
19. Equity in national policies for Australians with kidney disease
20. Transparency, trust and minimizing burden to increase recruitment and retention in trials: a systematic review
21. Patient experiences of sleep in dialysis: systematic review of qualitative studies
22. NAV-KIDS2 trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease
23. Partnering with patients and caregivers to enrich research and care in kidney disease: values and strategies.
24. Baseline characteristics of participants in the NAVKIDS2 trial: a patient navigator program in children with chronic kidney disease.
25. Patient and caregiver perspectives on blood pressure in children with chronic kidney disease.
26. Experiences and Perspectives of Transgender Youths in Accessing Health Care: A Systematic Review.
27. Qualitative research methods and its application in nephrology.
28. Standardised Outcomes in Nephrology - Chronic Kidney Disease (SONG-CKD): a protocol for establishing a core outcome set for adults with chronic kidney disease who do not require kidney replacement therapy.
29. Kidney transplant recipient perspectives on telehealth during the COVID‐19 pandemic.
30. Patient and caregiver perspectives on sleep in dialysis.
31. Perspectives on mental health among patients receiving dialysis.
32. A practical guide to interpreting and applying systematic reviews of qualitative studies in rheumatology.
33. Suspension and resumption of kidney transplant programmes during the COVID‐19 pandemic: perspectives from patients, caregivers and potential living donors – a qualitative study.
34. Patients' perspectives of pain in dialysis: systematic review and thematic synthesis of qualitative studies.
35. Harnessing hope: Key to engaging patients and families in research.
36. The critical role of mixed methods research in developing valid and reliable patient-reported outcome measures.
37. NAV-KIDS2 trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease.
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