A mutation in bilirubin uridine 5′-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A mutation in bilirubin uridine 5′-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II

Published:1993-07 Issue:1 Volume:105 Page:216-220
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Bosma Piter J.,Goldhoorn Bart,Oude Elferink Ronald P.J.,Sinaasappel Maarten,Oostra Ben A.,Jansen Peter L.M.

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference24 articles.

1. Congenital familial nonhaemolytic jaundice with kernicterus;Crigler;Pediatrics,1952

2. Hereditary jaundice and disorders of bilirubin metabolism;Wolkoff,1983

3. Hyperbilirubinemia;Smid,1978

4. Inherited disorders of bilirubin metabolism;Roy Chowdhury,1990

5. Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults;Arias;J Clin Invest,1962

Cited by 97 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. Human Hepatocyte Transplantation: Three Decades of Clinical Experience and Future Perspective;Stem Cells Translational Medicine;2023-12-16

2. Disorders of Bilirubin Metabolism;The Liver;2020-01-24

3. Bile Pigment Metabolism and Its Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

4. Uridine diphosphate glucuronosyltransferase 1A1;Xenobiotica;2019-06-03

5. Hyperbilirubinemia;Diagnosis of Liver Disease;2019

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP