Sporadic Hyperphosphatasia Syndrome Featuring Periostitis and Accelerated Skeletal Turnover without Receptor Activator of Nuclear Factor-κB, Osteoprotegerin, or Sequestosome-1 Gene Defects-Reference-Cited by-同舟云学术

Sporadic Hyperphosphatasia Syndrome Featuring Periostitis and Accelerated Skeletal Turnover without Receptor Activator of Nuclear Factor-κB, Osteoprotegerin, or Sequestosome-1 Gene Defects

Published:2007-05-01 Issue:5 Volume:92 Page:1897-1901
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Simsek Suat¹,Basoski Natalja M.²,Bravenboer Nathalie¹,Zhang Xiafang³,Mumm Steven³,Whyte Michael P.³⁴,Netelenbos J. Coen¹

Affiliation:

1. Department of Endocrinology (S.S., N.B., J.C.N.), VU University Medical Center, 1007 MB Amsterdam, The Netherlands

2. Department of Rheumatology (N.M.B.), VU University Medical Center, 1007 MB Amsterdam, The Netherlands

3. Division of Bone and Mineral Diseases (X.Z., S.M., M.P.W.), Washington University School of Medicine, St. Louis, Missouri 63110

4. Center for Metabolic Bone Disease and Molecular Research (S.M., M.P.W.), Shriners Hospitals for Children, St. Louis, Missouri 63131

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/92/5/1897/9055357/jcem1897.pdf

Reference36 articles.

1. Hyperphosphatasia syndromes;Cole;In: Cohen Jr MM, Baum BJ, eds. Studies in stomatology and craniofacial biology. Amsterdam: IOS Press;,1996

2. Heritable disorders of the RANKL/OPG/RANK signaling pathway.;Whyte;J Musculoskelet Neuronal Interact,2004

3. McKusick VA 2006 Online Mendelian inheritance in man, OMIM. Baltimore, MD: McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University, and Bethesda, MD: National Center for Biotechnology Information, National Library of Medicine. www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174810

4. Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis.;Hughes;Nat Genet,2000

5. Familial expansile osteolysis (excessive RANK effect) in a 5-generation American kindred.;Whyte;Medicine (Baltimore),2002

Cited by 4 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. Juvenile Paget disease;Metabolism;2018-03

2. Profound hypocalcemia following effective response to zoledronic acid treatment in a patient with juvenile Paget’s disease;Journal of Bone and Mineral Metabolism;2010-06-09

3. IKKβ activation is sufficient for RANK-independent osteoclast differentiation and osteolysis;Journal of Bone and Mineral Research;2010-02-01

4. Current World Literature;Current Opinion in Rheumatology;2008-01