EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)

Published:2015-07-08 Issue:4 Volume:24 Page:479-495
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Porto Graça,Brissot Pierre,Swinkels Dorine W,Zoller Heinz,Kamarainen Outi,Patton Simon,Alonso Isabel,Morris Michael,Keeney Steve

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2015128.pdf

Reference176 articles.

1. Fleming RE, Ponka P : Iron overload in human disease. N Engl J Med 2012; 366: 348–359.

2. Mayr R, Janecke AR, Schranz M et al: Ferroportin disease: a systematic meta-analysis of clinical and molecular findings. J Hepatol 2010; 53: 941–949.

3. European Association For The Study Of The Liver: EASL clinical practice guidelines for HFE hemochromatosis. J Hepatol 2010; 53: 3–22.

4. Bacon BR, Adams PC, Kowdley KV, Powell LW, Tavill AS : Diagnosis and management of hemochromatosis: 2011 practice guideline by the American Association for the Study of Liver Diseases. Hepatology 2011; 54: 328–343.

5. van Bokhoven MA, van Deursen CT, Swinkels DW : Diagnosis and management of hereditary haemochromatosis. BMJ 2011; 342: c7251.

Cited by 72 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. Exploring the interplay between iron metabolism imbalance and esophageal cancer;Oncologie;2024-07-01

2. Case report: A rare case of hereditary hemochromatosis caused by a mutation in the HAMP gene in Fuyang, China;Frontiers in Medicine;2024-06-28

3. Investigative algorithms for disorders affecting plasma transaminases (aspartate transaminase and alanine transaminase)—a narrative review;Journal of Laboratory and Precision Medicine;2024-04

4. A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis;Hepatology Forum;2024

5. Molecular testing in hemochromatosis;Diagnostic Molecular Pathology;2024

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

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3