Pain, quality of life, and coping in sickle cell disease.
about
Health related quality of life in sickle cell patients: the PiSCES projectChanges in coping, pain, and activity after cognitive-behavioral training: a randomized clinical trial for pediatric sickle cell disease using smartphones.Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress.Coping and coping assistance among children with sickle cell disease and their parentsSerum levels of leptin in Nigerian patients with sickle cell anaemia.Poor health related quality of life among patients of sickle cell disease.The role of stress and mood in sickle cell disease pain: an analysis of daily diary data.Commentary on the role of stress and mood in sickle cell disease pain: an analysis of daily diary data by laura s. Porter, karen m. Gil, james w. Carson, kelly k. Anthony, & jawana ready.Hydroxyurea for sickle cell disease.A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell diseaseHydroxyurea and sickle cell anemia: effect on quality of life.Parental problem-solving abilities and the association of sickle cell disease complications with health-related quality of life for school-age children.The Cellie Coping Kit for Sickle Cell Disease: Initial acceptability and feasibility.Health-related quality of life in children and adolescents with sickle cell diseaseObjective and subjective assessment of sleep in adolescents with chronic pain compared to healthy adolescents.Sleep quality and efficiency in adolescents with chronic pain: relationship with activity limitations and health-related quality of lifeHealth related quality of life among adolescents with sickle cell disease in Saudi ArabiaSensitization to acute procedural pain in pediatric sickle cell disease: modulation by painful vaso-occlusive episodes, age, and endothelin-1.Responsiveness of the PedsQL to pain-related changes in health-related quality of life in pediatric sickle cell disease.Evaluating the protective role of racial identity in children with sickle cell disease.The impact of chronic pain on adolescents: a review of previously used measures.The impact of iron overload and its treatment on quality of life: results from a literature review.Predictors of Academic Achievement for School Age Children with Sickle Cell Disease.Validation of the sickle cell disease pain burden interview-youth.Pain measurement as part of primary healthcare of adult patients with sickle cell disease.Psychosocial and pharmacological management of pain in pediatric sickle cell disease.Out with the bad and in with the good; red cell exchange, white cell reduction, and platelet reduction.Hydroxyurea (hydroxycarbamide) for sickle cell disease.Cognitive Testing of an Electronic Version of the Faces Pain Scale-Revised with Pediatric and Adolescent Sickle Cell Patients.Current Management in Sickle Cell Disease.Daily pain in adults with sickle cell disease-a different perspective.Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.Fast track admission for children with sickle cell crises. Should morphine or pethidine be given?The psychosocial impact of leg ulcers in patients with sickle cell disease: I don't want them to know my little secret.Perception of pain among pediatric patients with sickle cell pain crisis.Low adjusted-dose acenocoumarol therapy in sickle cell disease: a pilot study.Living with sickle cell disease: the perspective of young people.Predictive Ability of Intermittent Daily Sickle Cell Pain Assessment: The PiSCES Project.Design of the DOVE (Determining Effects of Platelet Inhibition on Vaso-Occlusive Events) trial: A global Phase 3 double-blind, randomized, placebo-controlled, multicenter study of the efficacy and safety of prasugrel in pediatric patients with sicklDifferences in quality of life between pediatric sickle cell patients who used hydroxyurea and those who did not.
P2860
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P2860
Pain, quality of life, and coping in sickle cell disease.
description
1996 nî lūn-bûn
@nan
1996 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Pain, quality of life, and coping in sickle cell disease.
@ast
Pain, quality of life, and coping in sickle cell disease.
@en
Pain, quality of life, and coping in sickle cell disease.
@nl
type
label
Pain, quality of life, and coping in sickle cell disease.
@ast
Pain, quality of life, and coping in sickle cell disease.
@en
Pain, quality of life, and coping in sickle cell disease.
@nl
prefLabel
Pain, quality of life, and coping in sickle cell disease.
@ast
Pain, quality of life, and coping in sickle cell disease.
@en
Pain, quality of life, and coping in sickle cell disease.
@nl
P2093
P356
P1476
Pain, quality of life, and coping in sickle cell disease.
@en
P2093
P2860
P304
P356
10.1136/ADC.75.3.199
P407
P577
1996-09-01T00:00:00Z