Musculoskeletal complications associated with lysosomal storage disorders: Gaucher disease and Hurler-Scheie syndrome (mucopolysaccharidosis type I)
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Rheumatology
Reference41 articles.
1. Enzyme replacement therapy: conception, chaos and culmination
2. Enzyme therapy for the lysosomal storage disorders: principles, patents, practice and prospects
3. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry
4. Substrate reduction therapy: miglustat as a remedy for symptomatic patients with Gaucher disease type 1
5. The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations
Cited by 70 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. Bone: A Neglected Endocrine Organ?;Journal of Clinical Medicine;2024-07-02
2. Wnt signaling pathway inhibitors, sclerostin and DKK-1, correlate with pain and bone pathology in patients with Gaucher disease;Frontiers in Endocrinology;2022-11-24
3. A Child Presenting with Mucopolysaccharidosis;Case Reports in Clinical Medicine;2022
4. Dual Cancer in a Patient with Type 1 Gaucher Disease: Case Report and Literature Review;Timisoara Medical Journal;2021-10-26
5. Ultrasound findings of finger, wrist and knee joints in Mucopolysaccharidosis Type I;Molecular Genetics and Metabolism;2021-07
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