New England consortium: A model for medical evaluation of expanded newborn screening with tandem mass spectrometry

Journal of Inherited Metabolic Disease

Volumn 24, Issue 2, 2001, Pages 303-304

  Albers, S ^a   Waisbren, S E ^b   Ampola, M G ^b   Brewster, T G ^b   Burke, L W ^b   Demmer, L A ^b   Filiano, J ^b   Greenstein, R M G ^b   Ingham, C L ^b   Korson, M S ^b   Marsden, D ^b   Schwartz, R C ^b   Seashore, M R ^b   Shih, V E ^b   Levy, H L ^b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE;

ARTICLE; FIRST AID; FOLLOW UP; HUMAN; INBORN ERROR OF METABOLISM; INFORMATION SYSTEM; MEDICAL ASSESSMENT; MEDICAL RESEARCH; MODEL; NEWBORN; NEWBORN SCREENING; PATIENT CARE; PEDIATRICS; PHYSICIAN ATTITUDE; PRIMARY MEDICAL CARE; PROSPECTIVE STUDY; RISK MANAGEMENT; SYMPTOM; TANDEM MASS SPECTROMETRY; UNITED STATES;

HUMANS; INFANT, NEWBORN; MASS SPECTROMETRY; METABOLISM, INBORN ERRORS; NEONATAL SCREENING; NEW ENGLAND;

EID: 0035005548     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1010391623104     Document Type: Article

References (2)

1. American Academy of Pediatrics Ad Hoc Task Force on Definition of the Medical Home. (1992) The medical home. Pediatrics 90: 774.
2. Levy HL, Albers S (2000) Genetic screening of newborns. In: Lander E, Lifton R, Page D, eds. Annual Review of Genomics and Human Genetics, vol. 1. Palo Alto: Annual Reviews, 139-177.