Literature DB >> 17587286

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

Kenichi Sugita1, Yoshihiro Maruo, Hidemitsu Kurosawa, Akira Tsuchioka, Toshio Fujiwara, Asami Mori, Hiroshi Ideguchi, Mitsuoki Eguchi.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2007        PMID： 17587286     DOI： 10.1111/j.1442-200X.2007.02410.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


× No keyword cloud information.
  5 in total

1.  Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.

Authors:  Shigeo Iijima; Takehiko Ohzeki; Yoshihiro Maruo
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759

2.  Severe unconjugated hyperbilirubinaemia: one and one makes three?

Authors:  Kushal Naha; Sowjanya Dasari; G Vivek; Manjunath Hande; Vasudev Acharya
Journal:  BMJ Case Rep       Date:  2013-06-18

3.  A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Authors:  Hee Jung Lee; Hee Seok Moon; Eaum Seok Lee; Seok Hyun Kim; Jae Kyu Sung; Byung Seok Lee; Hyun Yong Jeong; Heon Young Lee; Young Jae Eu
Journal:  Korean J Hepatol       Date:  2010-09

4.  Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.

Authors:  Joo Hyung Han; Seung Kim; Hoon Jang; So Won Kim; Min Goo Lee; Hong Koh; Ji Hyun Lee
Journal:  PLoS One       Date:  2015-06-24       Impact factor: 3.240

5.  Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

Authors:  Mitsuhiko Aiso; Minami Yagi; Atsushi Tanaka; Kotaro Miura; Ryo Miura; Toshihiko Arizumi; Yoriyuki Takamori; Sayuri Nakahara; Yoshihiro Maruo; Hajime Takikawa
Journal:  Intern Med       Date:  2017-03-17       Impact factor: 1.271
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.