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Journal Abstract Search

185 related items for PubMed ID: 26762549

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  • 5. Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.
    Saki F, Karamizadeh Z, Nasirabadi S, Mumm S, McAlister WH, Whyte MP.
    J Bone Miner Res; 2013 Jun; 28(6):1501-8. PubMed ID: 23322328
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  • 10. Juvenile Paget's disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype.
    Naot D, Wilson LC, Allgrove J, Adviento E, Piec I, Musson DS, Cundy T, Calder AD.
    Bone; 2020 Jan; 130():115098. PubMed ID: 31655221
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  • 12. Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.
    Brunetti G, Marzano F, Colucci S, Ventura A, Cavallo L, Grano M, Faienza MF.
    Endocrine; 2012 Oct; 42(2):266-71. PubMed ID: 22638612
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  • 13. Denosumab treatment for juvenile Paget's disease: results from two adult patients with osteoprotegerin deficiency ("Balkan" mutation in the TNFRSF11B gene).
    Polyzos SA, Singhellakis PN, Naot D, Adamidou F, Malandrinou FC, Anastasilakis AD, Polymerou V, Kita M.
    J Clin Endocrinol Metab; 2014 Mar; 99(3):703-7. PubMed ID: 24433001
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  • 18. Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapy.
    Craven M, Vajravelu ME, Shekdar KV, Levine MA, Mumm S, Whyte MP, Mancilla EE.
    Bone; 2023 May; 170():116698. PubMed ID: 36740137
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