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Hyperphosphatemic Familial Tumoral Calcinosis With Galnt3 Mutation: Transient Response to Anti‐Interleukin‐1 Treatments

Hyperphosphatemic familial tumoral calcinosis (HFTC) is a rare autosomal recessive disease caused by mutations in genes involved in phosphate homeostasis and characterized by high serum phosphate concentration and occurrence of ectopic calcifications. Management of the disease includes lowering of p...

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Bibliografske podrobnosti
izdano v:JBMR Plus
Main Authors: Dauchez, Astrid, Souffir, Camille, Quartier, Pierre, Baujat, Geneviève, Briot, Karine, Roux, Christian
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6659445/
https://ncbi.nlm.nih.gov/pubmed/31372591
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbm4.10185
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