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Volumn 37, Issue 8, 2015, Pages 577-583

Transitioning adolescents and young adults with sickle cell disease from pediatric to adult health care: Provider perspectives

Author keywords

Adolescent; Sickle cell anemia; Transition to adult care; Young adult

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATTITUDE TO HEALTH; CONTROLLED STUDY; DOCTOR PATIENT RELATION; EMOTIONAL STABILITY; FAMILY LIFE; FEMALE; HEALTH CARE UTILIZATION; HEALTH LITERACY; HEALTH PERSONNEL ATTITUDE; HEALTH STATUS; HUMAN; ILLNESS TRAJECTORY; MALE; MEDICAL EXPERT; MEDICATION COMPLIANCE; MOTIVATION; PATIENT CARE PLANNING; PATIENT COMFORT; PATIENT PARTICIPATION; PERSONAL EXPERIENCE; PRIORITY JOURNAL; PROFESSIONAL COMPETENCE; QUALITY OF LIFE; SEMI STRUCTURED INTERVIEW; SICKLE CELL ANEMIA; SOCIAL STATUS; SUPPORT GROUP; TRANSITION TO ADULT CARE; WORK EXPERIENCE; YOUNG ADULT; ANEMIA, SICKLE CELL; CHILD PARENT RELATION; CHILD PSYCHOLOGY; CLINICAL TRIAL; COGNITION DISORDERS; COMPLICATION; HEALTH CARE PERSONNEL; HUMAN RELATION; INTERVIEW; MULTICENTER STUDY; PATIENT ATTITUDE; PSYCHOLOGICAL MODEL; PSYCHOLOGY; QUALITATIVE RESEARCH; SOCIOECONOMICS; STROKE;

EID: 84945957913     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0000000000000427     Document Type: Article
Times cited : (49)

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