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Journal Abstract Search
254 related items for PubMed ID: 26772620
1. Development of a molecular test of Paget's disease of bone. Guay-Bélanger S, Simonyan D, Bureau A, Gagnon E, Albert C, Morissette J, Siris ES, Orcel P, Brown JP, Michou L. Bone; 2016 Mar; 84():213-221. PubMed ID: 26772620 [Abstract] [Full Text] [Related]
15. 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]
16. Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States. Rhodes EC, Johnson-Pais TL, Singer FR, Ankerst DP, Bruder JM, Wisdom J, Hoon DS, Lin E, Bone HG, Simcic KJ, Leach RJ. Calcif Tissue Int; 2008 Apr; 82(4):271-7. PubMed ID: 18379713 [Abstract] [Full Text] [Related]
18. Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin. Daroszewska A, Hocking LJ, McGuigan FE, Langdahl B, Stone MD, Cundy T, Nicholson GC, Fraser WD, Ralston SH. J Bone Miner Res; 2004 Sep; 19(9):1506-11. PubMed ID: 15312251 [Abstract] [Full Text] [Related]