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Van Buchem disease

Known as: Hyperostosis Corticalis Generalisata, VBCH, Sost Sclerosing Bone Dysplasia 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
Sclerosteosis and van Buchem disease (VBD) are two rare autosomal recessive disorders that results from osteoblast hyperactivity… Expand
Highly Cited
2013
Highly Cited
2013
Van Buchem disease (VBD) is a rare bone sclerosing dysplasia caused by the lack of a regulatory element of the SOST gene, which… Expand
Review
2011
Review
2011
Sclerosing bone dysplasias are skeletal abnormalities of varying severity with a wide range of radiologic, clinical, and genetic… Expand
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Highly Cited
2010
Highly Cited
2010
The recently identified type VI secretion system (T6SS) is implicated in the virulence of many Gram-negative bacteria… Expand
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2010
2010
SOST is a negative regulator of bone formation, and mutations in human SOST are responsible for sclerosteosis. In addition to… Expand
Highly Cited
2009
Highly Cited
2009
Sclerostin is an inhibitor of bone formation expressed by osteocytes. We hypothesized that sclerostin is expressed by cells of… Expand
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Highly Cited
2009
Highly Cited
2009
Edwardsiella tarda is a gram-negative pathogen for hemorrhagic septicemia in a broad range of hosts. The type VI secretion system… Expand
2009
2009
A combination of clinical and MR examinations should be used to assess the severity of Van Buchem disease, particularly in… Expand
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Highly Cited
1998
Highly Cited
1998
Van Buchem disease (hyperostosis corticalis generalisata; OMIM 239100 [http://www3.ncbi.nlm.nih. gov:80/htbin-post/Omim/dispmim… Expand
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1976
1976
  • R. Owen
  • The British journal of radiology
  • 1976
  • Corpus ID: 31913259
The features of Van Buchem's disease are described, affecting six members of one family, spanning three generations of ages from… Expand