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