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Volumn 49, Issue 6, 2015, Pages S528-S535

Connecting the Dots: Linking the National Program of Cancer Registries and the Needs of Survivors and Clinicians

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER MORTALITY; CANCER RECURRENCE; CANCER REGISTRY; CANCER SCREENING; CANCER STAGING; CANCER SURVIVOR; CANCER THERAPY; CLINICAL PRACTICE; CLINICAL RESEARCH; COMPARATIVE EFFECTIVENESS; DEMOGRAPHY; FOLLOW UP; HEALTH SURVEY; HUMAN; OUTCOMES RESEARCH; QUALITY CONTROL; TOTAL QUALITY MANAGEMENT; TREATMENT PLANNING; TUMOR VOLUME; ELECTRONIC HEALTH RECORD; INFORMATION DISSEMINATION; MEDICAL RESEARCH; NEOPLASMS; OUTCOME ASSESSMENT; PATIENT CARE PLANNING; PATIENT SELECTION; PUBLIC HEALTH; PUBLIC HEALTH SERVICE; REGISTER; SURVIVOR; UNITED STATES;

EID: 84955073883     PISSN: 07493797     EISSN: 18732607     Source Type: Journal    
DOI: 10.1016/j.amepre.2015.08.026     Document Type: Article
Times cited : (13)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.