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Journal Abstract Search

135 related items for PubMed ID: 25108083

  • 21. Loss of chaotic trabecular structure in OPG-deficient juvenile Paget's disease patients indicates a chaogenic role for OPG in nonlinear pattern formation of trabecular bone.
    Salmon P.
    J Bone Miner Res; 2004 May; 19(5):695-702. PubMed ID: 15068491
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  • 22. Serum osteoprotegerin and its ligand in Paget's disease of bone: relationship to disease activity and effect of treatment with bisphosphonates.
    Alvarez L, Peris P, Guañabens N, Vidal S, Ros I, Pons F, Filella X, Monegal A, Muñoz-Gomez J, Ballesta AM.
    Arthritis Rheum; 2003 Mar; 48(3):824-8. PubMed ID: 12632438
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  • 23. Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of bone.
    Beyens G, Daroszewska A, de Freitas F, Fransen E, Vanhoenacker F, Verbruggen L, Zmierczak HG, Westhovens R, Van Offel J, Ralston SH, Devogelaer JP, Van Hul W.
    J Bone Miner Res; 2007 Jul; 22(7):1062-71. PubMed ID: 17388729
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  • 24. Polymorphisms of CSF1 and TM7SF4 genes in a case of mild juvenile Paget's disease found using next-generation sequencing.
    Donáth J, Speer G, Kósa JP, Árvai K, Balla B, Juhász P, Lakatos P, Poór G.
    Croat Med J; 2015 Apr; 56(2):145-51. PubMed ID: 25891874
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  • 25. Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-kappaB, osteoprotegerin, or sequestosome-1 gene defects.
    Simsek S, Basoski NM, Bravenboer N, Zhang X, Mumm S, Whyte MP, Netelenbos JC.
    J Clin Endocrinol Metab; 2007 May; 92(5):1897-901. PubMed ID: 17284635
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  • 26. Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences.
    Hocking LJ, Lucas GJ, Daroszewska A, Cundy T, Nicholson GC, Donath J, Walsh JP, Finlayson C, Cavey JR, Ciani B, Sheppard PW, Searle MS, Layfield R, Ralston SH.
    J Bone Miner Res; 2004 Jul; 19(7):1122-7. PubMed ID: 15176995
    [Abstract] [Full Text] [Related]

  • 27. Effects of RANK-ligand antibody (denosumab) treatment on bone turnover markers in a girl with juvenile Paget's disease.
    Grasemann C, Schündeln MM, Hövel M, Schweiger B, Bergmann C, Herrmann R, Wieczorek D, Zabel B, Wieland R, Hauffa BP.
    J Clin Endocrinol Metab; 2013 Aug; 98(8):3121-6. PubMed ID: 23788687
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  • 31. A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype.
    Cundy T, Hegde M, Naot D, Chong B, King A, Wallace R, Mulley J, Love DR, Seidel J, Fawkner M, Banovic T, Callon KE, Grey AB, Reid IR, Middleton-Hardie CA, Cornish J.
    Hum Mol Genet; 2002 Sep 01; 11(18):2119-27. PubMed ID: 12189164
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  • 32. 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 01; 21 Suppl 2():P31-7. PubMed ID: 17229006
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  • 33. Recombinant osteoprotegerin for juvenile Paget's disease.
    Cundy T, Davidson J, Rutland MD, Stewart C, DePaoli AM.
    N Engl J Med; 2005 Sep 01; 353(9):918-23. PubMed ID: 16135836
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  • 35. Phenotypic characterization of early onset Paget's disease of bone caused by a 27-bp duplication in the TNFRSF11A gene.
    Nakatsuka K, Nishizawa Y, Ralston SH.
    J Bone Miner Res; 2003 Aug 01; 18(8):1381-5. PubMed ID: 12929927
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  • 36. Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family.
    Falchetti A, Di Stefano M, Marini F, Del Monte F, Gozzini A, Masi L, Tanini A, Amedei A, Carossino A, Isaia G, Brandi ML.
    Arthritis Res Ther; 2005 Aug 01; 7(6):R1289-95. PubMed ID: 16277682
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  • 38. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
    Whyte MP.
    Ann N Y Acad Sci; 2006 Apr 01; 1068():143-64. PubMed ID: 16831914
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  • 40. Mechanisms of disease: genetics of Paget's disease of bone and related disorders.
    Daroszewska A, Ralston SH.
    Nat Clin Pract Rheumatol; 2006 May 01; 2(5):270-7. PubMed ID: 16932700
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