39 results on '"Guha, Chandana"'
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2. 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
3. WCN24-1948 PERSPECTIVES OF CAREGIVERS ON ACCESS TO CARE FOR CHILDREN WITH CHRONIC KIDNEY DISEASE: A SEMI-STRUCTURED INTERVIEW STUDY
4. WCN24-1881 Interventions to improve life participation in kidney transplant recipients: a systematic review and meta-analysis
5. Consumer Involvement in Research and Decision-Making in Nephrology
6. Nephrologists’ perspectives on communication and decision-making regarding technique survival in peritoneal dialysis: an international qualitative interview study
7. Socioeconomic position and health among children and adolescents with chronic kidney disease across the life-course
8. Outcomes for clinical trials involving adults with chronic kidney disease: a multinational Delphi survey involving patients, caregivers and health professionals
9. Patient Perspectives on Clotting in the Extracorporeal Circuit and Decision-Making Regarding Anticoagulation Therapy
10. School attendance and sport participation amongst children with chronic kidney disease: a cross-sectional analysis from the Kids with CKD (KCAD) study
11. The Impact of the COVID-19 Pandemic on Patients With CKD: Systematic Review of Qualitative Studies
12. Socio-demographic drivers of donor and recipient gender disparities in living kidney donation in Australia.
13. Caring for the peritoneal dialysis catheter: Reflections on catheter and exit site care in peritoneal dialysis
14. Patients’ Perspectives, Factors, and Patterns of eHealth Use in Kidney Transplant Recipients
15. Longitudinal assessment of the health-related quality of life of children and adolescents with chronic kidney disease
16. Baseline characteristics of participants in the NAVKIDS2 trial: a patient navigator program in children with chronic kidney disease
17. 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
18. Perspectives of Clinicians on Shared Decision Making in Pediatric CKD: A Qualitative Study
19. Experiences and Perspectives of Transgender Youths in Accessing Health Care
20. Perspectives of solid organ transplant recipients on medicine-taking: Systematic review of qualitative studies
21. Patient navigator programmes for children and adolescents with chronic diseases
22. Establishing a core outcome measure for pain in patients with autosomal dominant polycystic kidney disease: a consensus workshop report
23. Kidney transplant recipient perspectives on telehealth during the COVID‐19 pandemic
24. Patient and caregiver perspectives on blood pressure in children with chronic kidney disease
25. Transparency, trust and minimizing burden to increase recruitment and retention in trials: a systematic review
26. Qualitative research methods and its application in nephrology
27. Equity in national policies for Australians with kidney disease
28. Patient experiences of sleep in dialysis: systematic review of qualitative studies
29. Harnessing hope: Key to engaging patients and families in research
30. A practical guide to interpreting and applying systematic reviews of qualitative studies in rheumatology
31. Patient needs and priorities for patient navigator programmes in chronic kidney disease: a workshop report
32. Perspectives on life participation by young adults with chronic kidney disease: an interview study
33. Developing Consensus-Based Outcome Domains for Trials in Children and Adolescents With CKD: An International Delphi Survey
34. Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology—Children and Adolescents (SONG-KIDS) consensus workshops
35. International Survey to Establish Prioritized Outcomes for Trials in People With Coronavirus Disease 2019
36. Suspension and resumption of kidney transplant programmes during the COVID‐19 pandemic: perspectives from patients, caregivers and potential living donors – a qualitative study
37. Patients' perspectives of pain in dialysis: systematic review and thematic synthesis of qualitative studies
38. Establishing a Core Outcome Set for Peritoneal Dialysis: Report of the SONG-PD (Standardized Outcomes in Nephrology–Peritoneal Dialysis) Consensus Workshop
39. 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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