An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference36 articles.
1. Congenital hyperphosphatasia. A clinical, pathological, and biochemical study of two cases;Eyring;J. Bone Joint Surg. Am.,1968
2. Chronic idiopathic hyperphosphatasia. Report of a case treated with pamidronate and a review of the literature;Spindler;J. Rheumatol.,1992
3. Multifocal osteogenic sarcoma of the skull in a patient who had congenital hyperphosphatasemic skeletal dysplasia. A case report;Nerlich;J. Bone Joint Surg. Am.,1992
4. Calcitonin treatment in osteoectasia with hyperphosphatasia (juvenile Paget's disease): radiographic changes after treatment;Tüysüz;Pediatr. Radiol.,1999
5. Fragile bones and macrocranium;Bakwin;J. Pediatr.,1956
Cited by 32 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. Identifying the effective combination of acupuncture and traditional Chinese medicinal herbs for postmenopausal osteoporosis therapy through studies of their molecular regulation of bone homeostasis;J TRADIT CHIN MED;2024
2. Biochemical characterization of a disease-causing human osteoprotegerin variant;Scientific Reports;2022-09-10
3. Rhizomelia and Impaired Linear Growth in a Girl with Juvenile Paget Disease: The Natural History of the Condition;Hormone Research in Paediatrics;2021
4. Rare Inherited forms of Paget’s Disease and Related Syndromes;Calcified Tissue International;2019-02-13
5. Juvenile Paget disease;Metabolism;2018-03
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