Lis Cordingley
0000-0001-7675-240X
University of Manchester
81 papers found
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Beliefs About Pain in Pediatric Inflammatory and Noninflammatory Chronic Musculoskeletal Conditions: A Scoping Review
‘That's what makes me better’: Investigating children and adolescents' experiences of pain communication with healthcare professionals in paediatric rheumatology
Identifying and managing psoriasis-associated comorbidities: the IMPACT research programme
“I just want to be normal” : A qualitative investigation of adolescents' coping goals when dealing with pain related to arthritis and the underlying parent‐adolescent personal models
Sleep disturbance and quality of life in Rheumatoid Arthritis: a prospective mobile health study (Preprint)
Implementation of the PsoWell™ Model for the Management of People with Complex Psoriasis
Changes in the illness perceptions of patients with rheumatoid arthritis over the first year of methotrexate therapy
Progress to Date in Advancing Stratified Medicine in Psoriasis
‘We’re the First Port of Call’ – Perspectives of Ambulance Staff on Responding to Deaths by Suicide: A Qualitative Study
Exploring what constitutes effective continued healthcare professional training: A qualitative study and the development of a training intervention component taxonomy.
Can we implement the new research agenda for mental health?
What are the barriers to physical activity in patients with chronic plaque psoriasis?
“Asking Too Much?”: Randomized N-of-1 Trial Exploring Patient Preferences and Measurement Reactivity to Frequent Use of Remote Multidimensional Pain Assessments in Children and Young People With Juvenile Idiopathic Arthritis
Experiences of support from primary care and perceived needs of parents bereaved by suicide: a qualitative study
Evaluation of the Impact of the PABBS Suicide Bereavement Training on Clinicians' Knowledge and Skills
The predictors of and reasons for non-adherence in an observational cohort of patients with rheumatoid arthritis commencing methotrexate.
“Reluctant to Assess Pain”: A Qualitative Study of Health Care Professionals’ Beliefs About the Role of Pain in Juvenile Idiopathic Arthritis
Quality of life and psychological impact in the photodermatoses: a systematic review
“Seeing Pain Differently”: A Qualitative Investigation Into the Differences and Similarities of Pain and Rheumatology Specialists’ Interpretation of Multidimensional Mobile Health Pain Data From Children and Young People With Juvenile Idiopathic Arthritis
Depressive symptoms, pain and disability for adolescent patients with juvenile idiopathic arthritis: results from the Childhood Arthritis Prospective Study
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