172 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. Establishing a Core Outcome Measure for Peritoneal Dialysis-related Peritonitis: A Standardized Outcomes in Nephrology—Peritoneal Dialysis Consensus Workshop Report
4. 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
5. Socioeconomic Position and Health Among Children and Adolescents With CKD Across the Life-Course
6. Baseline characteristics of participants in the NAVKIDS.sup.2 trial: a patient navigator program in children with chronic kidney disease
7. Report of the Standardized Outcomes in Nephrology-transplant Consensus Workshop on Establishing a Core Outcome Measure for Infection in Kidney Transplant Recipients
8. 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
9. Patient-Centered Research and Outcomes in Cancer and Kidney Transplantation
10. Patient-Centered Research and Innovation in Nephrology
11. Patient Perspectives on Clotting in the Extracorporeal Circuit and Decision-Making Regarding Anticoagulation Therapy
12. The Impact of the COVID-19 Pandemic on Patients With CKD: Systematic Review of Qualitative Studies
13. Sociodemographic Drivers of Donor and Recipient Gender Disparities in Living Kidney Donation in Australia
14. 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
15. Patients’ Perspectives, Factors, and Patterns of eHealth Use in Kidney Transplant Recipients
16. Consumer Involvement in Research and Decision-Making in Nephrology
17. WCN24-1948 PERSPECTIVES OF CAREGIVERS ON ACCESS TO CARE FOR CHILDREN WITH CHRONIC KIDNEY DISEASE: A SEMI-STRUCTURED INTERVIEW STUDY
18. WCN24-1881 Interventions to improve life participation in kidney transplant recipients: a systematic review and meta-analysis
19. Nephrologists’ perspectives on communication and decision-making regarding technique survival in peritoneal dialysis: an international qualitative interview study
20. Socioeconomic position and health among children and adolescents with chronic kidney disease across the life-course
21. 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
22. Perspectives on ability to work from patients’ receiving dialysis and caregivers: analysis of data from the global SONG initiative
23. Longitudinal assessment of the health-related quality of life of children and adolescents with chronic kidney disease
24. Outcomes for clinical trials involving adults with chronic kidney disease: a multinational Delphi survey involving patients, caregivers and health professionals
25. Patient Perspectives on Clotting in the Extracorporeal Circuit and Decision-Making Regarding Anticoagulation Therapy
26. Perspectives of solid organ transplant recipients on medicine-taking: Systematic review of qualitative studies
27. Equity in national policies for Australians with kidney disease
28. School attendance and sport participation amongst children with chronic kidney disease: a cross-sectional analysis from the Kids with CKD (KCAD) study
29. Transparency, trust and minimizing burden to increase recruitment and retention in trials: a systematic review
30. Patient experiences of sleep in dialysis: systematic review of qualitative studies
31. Socio-demographic drivers of donor and recipient gender disparities in living kidney donation in Australia.
32. Caring for the peritoneal dialysis catheter: Reflections on catheter and exit site care in peritoneal dialysis
33. International Survey to Establish Prioritized Outcomes for Trials in People With Coronavirus Disease 2019
34. Longitudinal assessment of the health-related quality of life of children and adolescents with chronic kidney disease
35. Patientsʼ perspectives of pain in dialysis: systematic review and thematic synthesis of qualitative studies
36. NAV-KIDS2 trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease
37. Partnering with patients and caregivers to enrich research and care in kidney disease: values and strategies.
38. Baseline characteristics of participants in the NAVKIDS2 trial: a patient navigator program in children with chronic kidney disease.
39. Baseline characteristics of participants in the NAVKIDS2 trial: a patient navigator program in children with chronic kidney disease
40. Perspectives of Clinicians on Shared Decision Making in Pediatric CKD: A Qualitative Study
41. Establishing a Core Outcome Measure for Peritoneal Dialysis-related Peritonitis: A Standardized Outcomes in Nephrology—Peritoneal Dialysis Consensus Workshop Report
42. Experiences and Perspectives of Transgender Youths in Accessing Health Care
43. Patient navigator programmes for children and adolescents with chronic diseases
44. Establishing a core outcome measure for pain in patients with autosomal dominant polycystic kidney disease: a consensus workshop report
45. Kidney transplant recipient perspectives on telehealth during the COVID‐19 pandemic
46. Patient and caregiver perspectives on blood pressure in children with chronic kidney disease
47. Qualitative research methods and its application in nephrology
48. Patient and caregiver perspectives on blood pressure in children with chronic kidney disease.
49. Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology—Children and Adolescents (SONG-KIDS) consensus workshops
50. Harnessing hope: Key to engaging patients and families in research
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