Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome-Reference-Cited by-同舟云学术

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Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome

Published:2007-08 Issue:4 Volume:49 Page:540-542
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatr Int

Author:

SUGITA KENICHI,MARUO YOSHIHIRO,KUROSAWA HIDEMITSU,TSUCHIOKA AKIRA,FUJIWARA TOSHIO,MORI ASAMI,IDEGUCHI HIROSHI,EGUCHI MITSUOKI

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2007.02410.x/fullpdf

Reference15 articles.

1. DOES GILBERT'S DISEASE EXIST?

2. Population studies on Gilbert's syndrome.

3. Membrane protein phosphorylation of intact normal and hereditary spherocytic erythrocytes.

4. Gilbert syndrome caused by a homozygousmissense mutation (Tyr486Asp) of bilirubinUDP-glucuronosyltransferase gene

5. Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

Cited by 11 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. A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1;Journal of Inflammation Research;2024-09

2. Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia;Internal Medicine;2017

3. Identification of a Novel p.Q1772X ANK1 Mutation in a Korean Family with Hereditary Spherocytosis;PLOS ONE;2015-06-24

4. A Case of Hereditary Spherocytosis Coexisting with Gilbert's Syndrome;The Korean Journal of Gastroenterology;2013

5. Inherited Deficient Conjugation of Bilirubin;Textbook of Clinical Pediatrics;2012

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