Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
about
Coping and coping assistance among children with sickle cell disease and their parentsHydroxyurea in children with sickle cell disease: practice patterns and barriers to utilization.Development and validation of the Youth Acute Pain Functional Ability Questionnaire (YAPFAQ).The impact of a multidisciplinary pain management model on sickle cell disease pain hospitalizationsEvaluation and Treatment of Sickle Cell Pain in the Emergency Department: Paths to a Better FutureHealth related quality of life among adolescents with sickle cell disease in Saudi ArabiaPedsQL™ sickle cell disease module: feasibility, reliability, and validity.Health-related quality of life in children with sickle cell disease using the child health questionnaireSaudi SCD patients' symptoms and quality of life relative to the number of ED visits.Responsiveness of the PedsQL to pain-related changes in health-related quality of life in pediatric sickle cell disease.Benchmarking pain outcomes for children with sickle cell disease hospitalized in a tertiary referral pediatric hospitalImpact of hydroxyurea on clinical events in the BABY HUG trial.Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.Initial Evaluation of the Pediatric PROMIS® Health Domains in Children and Adolescents With Sickle Cell DiseaseHealth-related quality of life in pediatric minor injury: reliability, validity, and responsiveness of the Pediatric Quality of Life Inventory in the emergency department.Mistrust of Pediatric Sickle Cell Disease Clinical Trials Research.Differences in health-related quality of life in children with sickle cell disease receiving hydroxyureaValidation of the sickle cell disease pain burden interview-youth.Responsiveness of PROMIS® Pediatric Measures to Hospitalizations for Sickle Pain and Subsequent Recovery.PedsQL™ Multidimensional Fatigue Scale in sickle cell disease: feasibility, reliability, and validityHealth-related quality of life in sickle cell disease: past, present, and future.Psychosocial and pharmacological management of pain in pediatric sickle cell disease.Impact of emergency department care on outcomes of acute pain events in children with sickle cell disease.Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use.Sickle cell disease: primum non nocere (first do no harm).Quality of life in patients with sickle cell disease.Using photovoice to explore the unique life perspectives of youth with sickle cell disease: a pilot study.HABIT, a Randomized Feasibility Trial to Increase Hydroxyurea Adherence, Suggests Improved Health-Related Quality of Life in Youths with Sickle Cell Disease.[Formula: see text]Executive functioning and health-related quality of life in pediatric sickle cell disease.Sickle cell disease: a natural model of acute and chronic pain.
P2860
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P2860
Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
@en
type
label
Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
@en
prefLabel
Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
@en
P2093
P2860
P356
P1476
Vaso-occlusive painful events in sickle cell disease: impact on child well-being.
@en
P2093
Amanda M Brandow
David C Brousseau
Julie A Panepinto
Nicholas M Pajewski
P2860
P356
10.1002/PBC.22222
P577
2010-01-01T00:00:00Z