An unusual case of Crigler-Najjar disease in the adult
Author:
Publisher
Elsevier BV
Subject
Hepatology
Reference23 articles.
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2. Bilirubin metabolism — State of the art;Schmid;Gastroenterology,1978
3. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency — Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity;Arias;Amer. J. Med.,1969
4. Quantitative separation and determination of bilirubin and conjugated bilirubin in human serum;Weber;Clin. Chim. Acta,1962
5. Determination of bilirubin in liver homogenates and serum with diazotized p-iodoaniline;Van Roy;Clin. Chim. Acta,1971
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome;BMC Pediatrics;2018-10-03
2. Assessment of UGT Polymorphisms and Neonatal Jaundice;Seminars in Perinatology;2011-06
3. Clinical Utility of Electrophysiological Evaluation in Crigler-Najjar Syndrome;Neuropediatrics;2007-08
4. Neurologic Perspectives of Crigler-Najjar Syndrome Type I;Journal of Child Neurology;1998-06
5. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man.;Journal of Biological Chemistry;1994-07
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