Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome

CONTEXT: Hajdu-Cheney syndrome (HJCYS) is a rare, multisystem bone disease caused by heterozygous mutations in the NOTCH2 gene. Histomorphometric and bone ultrastructural analyses in children have not been reported and sparse evidence exists on response to bisphosphonate (BP) therapy. OBJECTIVE: To...

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Bibliografske podrobnosti
izdano v:J Clin Endocrinol Metab
Main Authors: Sakka, Sophia, Gafni, Rachel I., Davies, Justin H., Clarke, Bart, Tebben, Peter, Samuels, Mark, Saraff, Vrinda, Klaushofer, Klaus, Fratzl-Zelman, Nadja, Roschger, Paul, Rauch, Frank, Högler, Wolfgang
Format: Artigo
Jezik:Inglês
Izdano: Endocrine Society 2017
Teme:
Clinical Research Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5673271/
https://ncbi.nlm.nih.gov/pubmed/28938420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2017-01102
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