Non-Invasive Liver Iron Quantification by SQUID-Biosusceptometry and Serum Ferritin Iron as New Diagnostic Parameters in Hereditary Hemochromatosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference24 articles.
1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat. Genet.,1996
2. The gene TFR2 is mutated in a new type of haemochromatosis to 7q22;2Camaschella;Nat. Genet.,2000
3. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene;Montosi;J. Clin. Invest.,2001
4. Global prevalence of putative haemochromatosis mutations;Merryweather-Clarke;J. Med. Genet.,1997
5. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis;Gottschalk;Tissue Antigens,1998
Cited by 45 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. Diagnosing iron deficiency: Controversies and novel metrics;Best Practice & Research Clinical Anaesthesiology;2023-11
2. Proteomic changes in broiler liver by body weight differences under chronic heat stress;Poultry Science;2022-05
3. Iron overload in the HCT patient: a review;Bone Marrow Transplantation;2021-03-29
4. Re-examining ferritin-bound iron: current and developing clinical tools;Clinical Chemistry and Laboratory Medicine (CCLM);2020-10-22
5. Susceptibility based multiparametric quantification of liver disease: Non-invasive evaluation of steatosis and iron overload;Magnetic Resonance Imaging;2019-11
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