Quality of life and impact of the disease on primary caregivers of juvenile idiopathic arthritis patients

Joint Bone Spine

Volumn 75, Issue 2, 2008, Pages 149-154

  Bruns, Alessandra ^a   Hilário, Maria Odete Esteves ^a   Jennings, Fabio ^a   Silva, Clovis Artur ^b   Natour, Jamil ^a  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Arthritis; Burden of disease; Caregivers; Juvenile idiopathic arthritis; Quality of life

Indexed keywords

ADOLESCENT; ARTICLE; CAREGIVER; CHILD; FEMALE; HEALTH STATUS; HEALTH SURVEY; HUMAN; INFANT; JUVENILE RHEUMATOID ARTHRITIS; LOWEST INCOME GROUP; MAJOR CLINICAL STUDY; MENTAL HEALTH; MENTAL TEST; NEWBORN; PSYCHOLOGIC ASSESSMENT; QUALITY OF LIFE; QUESTIONNAIRE; SCREENING TEST; SOCIOECONOMICS; STATISTICAL SIGNIFICANCE;

ADOLESCENT; ADULT; ARTHRITIS, JUVENILE RHEUMATOID; CAREGIVERS; CHILD; COST OF ILLNESS; FAMILY HEALTH; FEMALE; HEALTH SURVEYS; HUMANS; MALE; MIDDLE AGED; OUTCOME ASSESSMENT (HEALTH CARE); QUALITY OF LIFE; REGRESSION ANALYSIS; SICKNESS IMPACT PROFILE; SOCIAL CLASS;

EID: 40949091428     PISSN: 1297319X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbspin.2007.07.007     Document Type: Article

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