Improving surveillance for hyperammonemia in the newborn

Molecular Genetics and Metabolism

Volumn 110, Issue 1-2, 2013, Pages 102-105

  Vergano, Samantha A ^a   Crossette, Jonathan M ^a   Cusick, Frederick C ^a   Desai, Bimal R ^a,b   Deardorff, Matthew A ^a,b   Sondheimer, Neal ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Electronic medical record; Infant; Screening; Urea cycle defect

Indexed keywords

AMMONIA; UREA;

AMMONIA BLOOD LEVEL; ARTICLE; BLOOD GAS; CHILD HOSPITALIZATION; CLINICAL ARTICLE; COHORT ANALYSIS; DISEASE SURVEILLANCE; ELECTRONIC MEDICAL RECORD; HEALTH CARE UTILIZATION; HUMAN; HYPERAMMONEMIA; NEWBORN; NEWBORN DISEASE; NEWBORN SCREENING; NEWBORN SURGERY; PHYSICIAN; PRIORITY JOURNAL; RETROSPECTIVE STUDY; EPIDEMIOLOGICAL MONITORING; FEMALE; INFANT; MALE; METABOLISM; PATHOLOGY;

AMMONIA; ELECTRONIC HEALTH RECORDS; EPIDEMIOLOGICAL MONITORING; FEMALE; HUMANS; HYPERAMMONEMIA; INFANT; INFANT, NEWBORN; MALE; RETROSPECTIVE STUDIES; UREA;

EID: 84882863909     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2013.05.005     Document Type: Article

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