46 results on '"Livermore, Polly"'
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2. Understanding the lived experience and psychosocial needs of children and young people with Juvenile Dermatomyositis : a mixed methods study
3. Gaining consensus on emotional wellbeing themes and preferences for digital intervention type and content to support the mental health of young people with long‐term health conditions: A Delphi study
4. P092 Empowering Parents: Navigating the Healthcare Journey as Nurses, Pharmacists, Therapists, Educators, Psychologists and Partners
5. Using poetry to illuminate the lived accounts of Juvenile Dermatomyositis in children and young people
6. Mental health in paediatric and adult myositis-related diseases: current state of research, interventions, and future steps from the MIHRA Psychological Impact Scientific Working Group
7. Beyond aches and pain: the hidden economic burden of musculoskeletal conditions in children and adolescents
8. Evaluating a competency framework for rheumatology nurses
9. Towards a consensus for nurse education of methotrexate for people with rheumatic and musculoskeletal diseases: A scoping review
10. 4 AHPs – making a difference through clinical research
11. 86 Musical moments from childhood to musical meetings with a baby: listening to parent voices on music therapy on the neonatal unit
12. 11 First steps in research-pre doctoral NIHR fellowships at GOSH
13. 55 Enhancing cardiac patient discharge through better use of digital systems: a systems improvement project
14. Being on the juvenile dermatomyositis rollercoaster: a qualitative study
15. Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
16. The standards for nurse education on Methotrexate for patients with Rheumatic and Musculoskeletal Diseases: a scoping review protocol
17. OA27 Growth of the UK and Ireland paediatric rheumatology nurses’ group
18. The benefits of a peer-support group for paediatric rheumatology nurses working in isolation
19. P087 RCN Rheumatology Nurse Competency Framework a reliable tool to improve quality care and set standards for education of nurses
20. Juvenile dermatomyositis. Where are we now?
21. 83 Children and caregiver experiences of taking part in clinical trials – results from the great ormond street hospital clinical research facility patient research experience survey
22. Mapping the current psychology provision for children and young people with juvenile dermatomyositis
23. Autologous T cell depleted haematopoietic stem cell transplantation in children with severe juvenile idiopathic arthritis in the UK (2000–2007)
24. British Society for Rheumatology guideline on management of paediatric, adolescent and adult patients with idiopathic inflammatory myopathy.
25. A survey to understand the feelings towards and impact of COVID-19 on the households of juvenile dermato myositis patients from a parent or carer perspective
26. 69 ‘The importance of peer-support for clinical academics at great ormond street children’s hospital’
27. The Use of Emerging Biological Treatments in Children
28. Teaching home administration of sub-cutaneous methotrexate: Polly Livermore describes the successful implementation of a teaching package to prepare parents to administer methotrexate to their children with rheumatic disease. (Clinical)
29. P99 National competency framework for rheumatology nurse specialists
30. ‘Reducing anxiety and maintaining care’ during the COVID-19 pandemic
31. 37 Using research poems to share experiences of having a complex health condition
32. Additional file 5: of Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
33. Additional file 2: of Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
34. Additional file 3: of Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
35. Additional file 1: of Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
36. Additional file 4: of Development of a benchmarking toolkit for adolescent and young adult rheumatology services (BeTAR)
37. survey to understand the feelings towards and impact of COVID-19 on the households of juvenile dermato myositis patients from a parent or carer perspective.
38. benefits of a peer-support group for paediatric rheumatology nurses working in isolation.
39. R11 Understanding juvenile dermatomyositis from a young person’s perspective
40. 33. Developing a toolkit to benchmark young person friendly services for patients with autoimmune rheumatic disease
41. 289. DEVELOPING A TOOLKIT TO BENCHMARK YOUNG PERSON–FRIENDLY SERVICES FOR PATIENTS WITH AUTOIMMUNE RHEUMATIC DISEASE
42. Open label phase II trial of single, ascending doses of MRA in Caucasian children with severe systemic juvenile idiopathic arthritis: proof of principle of the efficacy of IL-6 receptor blockade in this type of arthritis and demonstration of prolonged clinical improvement
43. Juvenile idiopathic arthritis: updated guide to administering methotrexate
44. Designing, Developing, and Testing a Chatbot for Parents and Caregivers of Children and Young People With Rheumatological Conditions (the IMPACT Study): Protocol for a Co-Designed Proof-of-Concept Study.
45. Adoption of technology enabled care to support the management of children and teenagers in rheumatology services: a protocol for a mixed-methods systematic review.
46. Beyond aches and pain: the hidden economic burden of musculoskeletal conditions in children and adolescents.
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