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Volumn 16, Issue 6, 2013, Pages 259-267

New and evolving rare diseases research programs at the national institutes of health

Author keywords

Biospecimens; Common data elements; Orphan drugs; Patient advocacy groups; Patient registries; Rare and genetic diseases research; Research network; Undiagnosed diseases

Indexed keywords

ACCESS TO INFORMATION; ARTICLE; CLINICAL DATA REPOSITORY; CLINICAL RESEARCH; DATA BASE; DISEASE REGISTRY; DRUG EFFICACY; DRUG SCREENING; DRUG TOXICITY; EDUCATION PROGRAM; FINANCIAL MANAGEMENT; FUNDING; GENETIC DISORDER; HOSPITAL; HUMAN; INFORMATION CENTER; INTERVENTION STUDY; MEDICAL EDUCATION; MEDICAL RESEARCH; NATIONAL HEALTH ORGANIZATION; NEGLECTED DISEASE; PATIENT ADVOCACY; POINT OF CARE TESTING; PRIORITY JOURNAL; RARE DISEASE; RESEARCH PRIORITY; THERAPY EFFECT; TRANSLATIONAL RESEARCH; COOPERATION; DRUG INDUSTRY; FACTUAL DATABASE; PUBLIC-PRIVATE PARTNERSHIP; REGISTER; UNITED STATES;

EID: 84899940552     PISSN: 16624246     EISSN: 16628063     Source Type: Journal    
DOI: 10.1159/000355929     Document Type: Article
Times cited : (16)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.