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Journal Abstract Search

319 related items for PubMed ID: 15312251

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  • 3. Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders.
    Lucas GJ, Daroszewska A, Ralston SH.
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P31-7. PubMed ID: 17229006
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  • 5. Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels.
    Whyte MP, Singhellakis PN, Petersen MB, Davies M, Totty WG, Mumm S.
    J Bone Miner Res; 2007 Jun; 22(6):938-46. PubMed ID: 17352649
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  • 6. Polymorphisms in the osteoprotegerin gene are associated with osteoporotic fractures.
    Langdahl BL, Carstens M, Stenkjaer L, Eriksen EF.
    J Bone Miner Res; 2002 Jul; 17(7):1245-55. PubMed ID: 12096838
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  • 7. Genetics of Paget's disease of bone.
    Daroszewska A, Ralston SH.
    Clin Sci (Lond); 2005 Sep; 109(3):257-63. PubMed ID: 16104845
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  • 8. Osteoprotegerin deficiency and juvenile Paget's disease.
    Whyte MP, Obrecht SE, Finnegan PM, Jones JL, Podgornik MN, McAlister WH, Mumm S.
    N Engl J Med; 2002 Jul 18; 347(3):175-84. PubMed ID: 12124406
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  • 9. Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.
    Lucas GJ, Hocking LJ, Daroszewska A, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Meier C, Hooper MJ, Ralston SH.
    J Bone Miner Res; 2005 Feb 18; 20(2):227-31. PubMed ID: 15647816
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  • 10. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
    Whyte MP.
    Ann N Y Acad Sci; 2006 Apr 18; 1068():143-64. PubMed ID: 16831914
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  • 11. An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation.
    Janssens K, de Vernejoul MC, de Freitas F, Vanhoenacker F, Van Hul W.
    Bone; 2005 Mar 18; 36(3):542-8. PubMed ID: 15777670
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  • 15. Evidence for increased clinical severity of familial and sporadic Paget's disease of bone in Campania, southern Italy.
    Rendina D, Gennari L, De Filippo G, Merlotti D, de Campora E, Fazioli F, Scarano G, Nuti R, Strazzullo P, Mossetti G.
    J Bone Miner Res; 2006 Dec 18; 21(12):1828-35. PubMed ID: 17002563
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  • 17. Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease.
    Beyens G, Van Hul E, Van Driessche K, Fransen E, Devogelaer JP, Vanhoenacker F, Van Offel J, Verbruggen L, De Clerck L, Westhovens R, Van Hul W.
    Calcif Tissue Int; 2004 Aug 18; 75(2):144-52. PubMed ID: 15164150
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