A prospective study of the role of coping and family functioning in health outcomes for adolescents with sickle cell disease

Journal of Pediatric Hematology/Oncology

Volumn 29, Issue 11, 2007, Pages 752-760

  Barakat, Lamia P ^a,b   Patterson, Chavis A ^b   Weinberger, Beverley Slome ^a   Simon, Katherine ^a   Gonzalez, Elizabeth R ^a   Dampier, Carlton ^b  

^a DREXEL UNIVERSITY   (United States)

^b DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

Family functioning; Pediatric sickle cell disease; Sociodemographic risk

Indexed keywords

ADAPTIVE BEHAVIOR; ADOLESCENT; ADULT; ARTICLE; CAREGIVER; CLINICAL ARTICLE; CONTROLLED STUDY; COPING BEHAVIOR; DEMOGRAPHY; DISEASE ASSOCIATION; DISEASE SEVERITY; FAMILY FUNCTIONING; FEMALE; HEALTH CARE UTILIZATION; HEMOGLOBIN BLOOD LEVEL; HUMAN; MALE; MEASUREMENT; MEDICAL RECORD REVIEW; NORMAL HUMAN; OUTCOME ASSESSMENT; PARENTAL STRESS; PRIORITY JOURNAL; PROSPECTIVE STUDY; RISK FACTOR; SCHOOL CHILD; SIBLING; SICKLE CELL ANEMIA; SOCIAL PSYCHOLOGY;

ADAPTATION, PSYCHOLOGICAL; ADOLESCENT; ANEMIA, SICKLE CELL; FAMILY; HUMANS; PARENTING; PROGNOSIS; PROSPECTIVE STUDIES; STRESS, PSYCHOLOGICAL;

EID: 35948963663     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e318157fdac     Document Type: Article

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