Bilirubin Genetics for the Nongeneticist: Hereditary Defects of Neonatal Bilirubin Conjugation-Reference-Cited by-同舟云学术

Bilirubin Genetics for the Nongeneticist: Hereditary Defects of Neonatal Bilirubin Conjugation

Published:2003-04-01 Issue:4 Volume:111 Page:886-893
ISSN:0031-4005
Container-title:Pediatrics
language:en
Short-container-title:

Author:

Kaplan Michael¹,Hammerman Cathy²,Maisels M. Jeffrey³

Affiliation:

1. Department of Neonatology  Shaare Zedek Medical Center  Faculty of Medicine of the Hebrew University  Jerusalem 91031, Israel

2. Department of Neonatology  Shaare Zedek Medical Center  Jerusalem 91031, Israel  Faculty of Health Sciences  Ben Gurion University of the Negev  Beer Sheva 84105, Israel

3. Department of Pediatrics  William Beaumont Hospital  Royal Oak, MI 48073-6769

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Link

https://publications.aap.org/pediatrics/article-pdf/111/4/886/1005281/pe0403000886.pdf

Reference66 articles.

1. Dennery PA, Seidman DS, Stevenson DK. Neonatal hyperbilirubinemia. N Engl J Med.2001;344:581–590

2. Iyanagi T, Emi Y, Ikushiro S-I. Biochemical and molecular aspects of genetic disorders of bilirubin metabolism. Biochim Biophys Acta.1998;1407:173–184

3. Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Hum Mutat.2000;16:297–306

4. Clarke DJ, Moghrabi N, Monaghan G, et al. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias. Clin Chim Acta.1997;266:63–74

5. Sampietro M, Iolascon A. Molecular pathology of Crigler-Najjar type I and II and Gilbert’s syndromes. Haematologica.1999;84:150–157

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