Long-term follow-up data collection and use in state newborn screening programs

Archives of Pediatrics and Adolescent Medicine

Volumn 161, Issue 10, 2007, Pages 994-1000

  Hoff, Timothy ^a,c   Ayoob, Maria ^a   Therrell, Bradford L ^b  

^a STATE UNIVERSITY OF NEW YORK   (United States)

^b National Newborn Screening and Genetics Resource Center   (United States)

^c UNIVERSITY AT ALBANY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL PRACTICE; ELECTRONICS; FOLLOW UP; HEALTH CARE PERSONNEL; HEALTH CARE POLICY; HEALTH CARE QUALITY; HEALTH PROGRAM; HEALTH STATUS; HEALTH SURVEY; HUMAN; INFORMATION PROCESSING; LONG TERM CARE; MEDICAL INFORMATION; NEWBORN DISEASE; NEWBORN SCREENING; OUTCOME ASSESSMENT; PRIORITY JOURNAL; QUESTIONNAIRE; VERBAL COMMUNICATION;

CONTINUITY OF PATIENT CARE; DATA COLLECTION; FEMALE; HEALTH CARE SURVEYS; HEALTH POLICY; HUMANS; INFANT WELFARE; INFANT, NEWBORN; INTERNET; MALE; NEONATAL SCREENING; OUTCOME ASSESSMENT (HEALTH CARE); PROGRAM DEVELOPMENT; PROGRAM EVALUATION; PUBLIC HEALTH ADMINISTRATION; PUBLIC HEALTH INFORMATICS; STATE HEALTH PLANS; TIME FACTORS; UNITED STATES;

EID: 34948822964     PISSN: 10724710     EISSN: 15383628     Source Type: Journal    
DOI: 10.1001/archpedi.161.10.994     Document Type: Article

References (13)

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