Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert's syndrome;Défice de glicose-6-fosfato desidrogenase, ictericia neonatal e sindroma de Gilbert

Acta Medica Portuguesa

Volumn 15, Issue 6, 2002, Pages 409-412

  Costa, Elísio ^a   Vieira, Emilia ^a   Cleto, Esmeralda ^a   Cabeda, José M ^a   Pinho, Luciana ^a   Coimbra, Eduarda ^a   Dos Santos, Rosário ^a   Barbot, José ^a  

^a HOSPITAL MARIA PIA   (Portugal)

Author keywords

G6PD; Jaundice; Neonatal Hyperbilirubinemia; Polymorphism; TATA box; UGT1A1

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUCURONOSYLTRANSFERASE;

ADOLESCENT; ALLELE; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EXCHANGE BLOOD TRANSFUSION; GENETIC ANALYSIS; GENETIC VARIABILITY; GILBERT DISEASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYTIC ANEMIA; HUMAN; INCIDENCE; INFANT; NEWBORN JAUNDICE; PROMOTER REGION;

ADOLESCENT; ALLELES; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC; CHILD; CHILD, PRESCHOOL; FEMALE; GENE FREQUENCY; GILBERT DISEASE; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCURONOSYLTRANSFERASE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; JAUNDICE; JAUNDICE, NEONATAL; MALE;

EID: 0036869792     PISSN: None     EISSN: 16460758     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

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