An uncommon cause of early infantile liver disease and raised chitotriosidase-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

An uncommon cause of early infantile liver disease and raised chitotriosidase

Published:2020-04-15 Issue:1 Volume:54 Page:22-24
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Sreekantam Srividya¹,Rizvi Hina²,Brown Rachel³,Santra Saikat¹,Raiman Julian¹,Vijay Suresh¹,Mckiernan Patrick J.⁴,Gupte Girish L.²

Affiliation:

1. Department of Clinical Inherited Metabolic DisordersBirmingham Women's and Children's Hospital NHS Trust UK

2. Department of HepatologyBirmingham Women's and Children's Hospital NHS Trust UK

3. Department of HistopathologyBirmingham Women's and Children's Hospital NHS Trust UK

4. Department of Gastroenterology, Hepatology, and NutritionChildren's Hospital of Pittsburgh Pittsburgh Pennsylvania USA

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12123

Reference4 articles.

1. A Rare Cause of Elevated Chitotriosidase Activity: Glycogen Storage Disease Type IV

2. The expanding spectrum of disorders with elevated plasma chitotriosidase activity:An update

3. Liver transplantation for glycogen storage disease types I, III, and IV;Matern D;Eur J Pediatr,1999

4. Analysis of GBE1 mutations via protein expression studies in glycogen storage disease type IV: A report on a non-progressive form with a literature review

Cited by 5 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 Rare Cause of Cirrhosis in a Toddler;Annals of Pediatric Gastroenterology and Hepatology ISPGHAN;2023-10-18

2. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource;Molecular Genetics and Metabolism;2023-03

3. SMPD1 gene variants in patients with β-Thalassemia major;Molecular Biology Reports;2023-02-01

4. A novel approach to characterize phenotypic variation in GSD IV: Reconceptualizing the clinical continuum;Frontiers in Genetics;2022-09-13

5. Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI;Orphanet Journal of Rare Diseases;2022-06-20

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