Causes of hemolysis in neonates with extreme hyperbilirubinemia

Journal of Perinatology

Volumn 34, Issue 8, 2014, Pages 616-619

  Christensen, R D ^a   Nussenzveig, R H ^b   Yaish, H M ^c,d   Henry, E ^a   Eggert, L D ^a   Agarwal, A M ^b  

^a Women and Newborns Program   (United States)

^b ARUP LABORATORIES   (United States)

^c PRIMARY CHILDREN'S MEDICAL CENTER   (United States)

^d UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; PYRUVATE KINASE;

ARTICLE; BILIRUBIN BLOOD LEVEL; CLINICAL ARTICLE; ERYTHROCYTE MEMBRANE; ERYTHROCYTE STRUCTURE; FLOW CYTOMETRY; HEMOLYSIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HUMAN CELL; NEONATAL HYPERBILIRUBINEMIA; NEWBORN; NEWBORN HEMOLYTIC DISEASE; NEWBORN JAUNDICE; NEXT GENERATION SEQUENCING; PHOTOTHERAPY; PROTEIN DEFICIENCY; PYRUVATE KINASE DEFICIENCY; SEQUENCE ANALYSIS; ANEMIA, HEMOLYTIC, CONGENITAL; BLOOD; CLINICAL PROTOCOL; COHORT ANALYSIS; ERYTHROBLASTOSIS, FETAL; GENETIC SCREENING; GENETICS; HYPERBILIRUBINEMIA, NEONATAL; NEWBORN SCREENING; TOTAL QUALITY MANAGEMENT;

ANEMIA, HEMOLYTIC, CONGENITAL; BILIRUBIN; CLINICAL PROTOCOLS; COHORT STUDIES; ERYTHROBLASTOSIS, FETAL; GENETIC TESTING; HEMOLYSIS; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; NEONATAL SCREENING; QUALITY IMPROVEMENT;

EID: 84905243262     PISSN: 07438346     EISSN: 14765543     Source Type: Journal    
DOI: 10.1038/jp.2014.68     Document Type: Article

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