Extending the Spectrum of Radiological Findings in Patients With Severe Osteopetrosis and Different Genetic Backgrounds-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Extending the Spectrum of Radiological Findings in Patients With Severe Osteopetrosis and Different Genetic Backgrounds

Published:2016-03-10 Issue:7 Volume:63 Page:1222-1226
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Simanovsky Natalia¹,Rozovsky Katya¹,Hiller Nurith¹,Weintraub Michael²,Stepensky Polina²

Affiliation:

1. Department of Medical Imaging; Hadassah Hebrew University Medical Center; Jerusalem Israel

2. Department of Pediatric Hematology-Oncology and Bone Marrow Transplantation; Hadassah Hebrew University Medical Center; Jerusalem Israel

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.25952/fullpdf

Reference18 articles.

1. Osteopetrosis: Genetics, treatment and new insights into osteoclast function;Sobacchi;Nat Rev Endocrinol,2013

2. Osteopetrosis;Stark;Orphanet J Rare Dis,2009

3. Osteopetrosis in children: A report of 26 cases;Loría-Cortés;J Pediatr,1977

4. Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: The unique splice site mutation in TCIRG1 gene spread by the founder effect;Bliznetz;Eur J Hum Genet,2009

5. Radiologic resolution of malignant infantile osteopetrosis skeletal changes following hematopoietic stem cell transplantation;Hashemi Taheri;Pediatr Blood Cancer,2015

Cited by 17 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. The molecular spectrum of Turkish osteopetrosis and related osteoclast disorders with natural history, including a candidate gene, CCDC120;Bone;2023-12

2. Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report;Journal of Pediatric Endocrinology and Metabolism;2023-05-05

3. MARBLE DISEASE (CASE REPORT);Wiadomości Lekarskie;2023

4. Osteoclast rich osteopetrosis due to defects in the TCIRG1 gene;Bone;2022-12

5. Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking;Bone;2022-11

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