about
Treatment of dental complications in sickle cell diseaseTreatment of dental complications in sickle cell diseaseAdult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.Depression and functioning in relation to health care use in sickle cell diseaseDepression and loneliness in Jamaicans with sickle cell diseaseRisk and resilience factors for grade retention in youth with sickle cell disease.The role of stress and mood in sickle cell disease pain: an analysis of daily diary data.Association between elevated depressive symptoms and clinical disease severity in African-American adults with sickle cell disease.Sickle cell anemia and dental caries: a literature review and pilot study.Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease.Emerging biobehavioral factors of fatigue in sickle cell diseaseScreening for depression in a hepatitis C population: the reliability and validity of the Center for Epidemiologic Studies Depression Scale (CES-D).Health-related stigma in young adults with sickle cell disease.Prevalence and psychosocial correlates of depressive symptoms among adolescents and adults with Klinefelter syndrome.Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival.Psychological complications in sickle cell disease.Prevalence of psychological symptoms among adults with sickle cell disease in Korle-Bu Teaching Hospital, Ghana.The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust studyAcute Pain and Depressive Symptoms: Independent Predictors of Insomnia Symptoms among Adults with Sickle Cell Disease.A preliminary study of psychiatric, familial, and medical characteristics of high-utilizing sickle cell disease patientsUtility of WHOQOL-BREF in measuring quality of life in sickle cell diseaseA biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.Socio-demographic characteristics and psychosocial consequences of sickle cell disease: the case of patients in a public hospital in GhanaAdolescents with life-threatening illnesses.Chronic Opioid Therapy and Central Sensitization in Sickle Cell Disease.A systematic review of the association between depression and health care utilization in children and adults with sickle cell disease.Increased rates of body dissatisfaction, depressive symptoms, and suicide attempts in Jamaican teens with sickle cell disease.The lives of adults over 30 living with sickle cell disorder.Impact of psychiatric diagnoses on hospital length of stay in children with sickle cell anemia.Prospective analysis of depression during peginterferon and ribavirin therapy of chronic hepatitis C: results of the Virahep-C study.Sickle cell disease: a stigmatizing condition that may lead to depression.Validation of the SF-36 in Jamaicans with sickle-cell disease.Predictors of health-related quality of life over time among adolescents and young adults with sickle cell disease.Depressive symptoms and sickle cell pain: The moderating role of internalized stigma.The severity of psychiatric disorders
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Depression, disease severity, and sickle cell disease.
@en
type
label
Depression, disease severity, and sickle cell disease.
@en
prefLabel
Depression, disease severity, and sickle cell disease.
@en
P2093
P356
P1476
Depression, disease severity, and sickle cell disease.
@en
P2093
Burchinal M
Orringer E
Strayhorn D
Wison Schaeffer JJ
P2888
P304
P356
10.1023/A:1018755831101
P577
1999-04-01T00:00:00Z
P6179
1009198836