Gilbert's syndrome is not associated with HELLP syndrome

British Journal of Obstetrics and Gynaecology

Volumn 108, Issue 9, 2001, Pages 1003-1004

  Zusterzeel, Petra L M ^a   Te Morsche, René ^a   Raijmakers, Maarten T M ^a   Peters, Wilbert H M ^a   Steegers, Eric A P ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE; URIDINE DIPHOSPHATE;

ARTICLE; CAUCASIAN; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC CODE; GENETIC DISORDER; GILBERT DISEASE; HELLP SYNDROME; HISTORY OF MEDICINE; HOMOZYGOSITY; HUMAN; MEDICAL ASSESSMENT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; TATA BOX;

BILIRUBIN; FEMALE; GENOTYPE; GILBERT DISEASE; HELLP SYNDROME; HUMANS; POLYMORPHISM, GENETIC; PREGNANCY; TATA BOX;

EID: 0034884689     PISSN: 03065456     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-5456(01)00233-9     Document Type: Article

References (5)

1. Liver function following pregnancy complicated by the HELLP syndrome
2. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
3. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promotor region of the UGT1A1 gene
4. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome
5. Hereditary jaundice and disorders of bilirubin metabolism