-
3
-
-
53349165206
-
Pathogenesis of Paget's disease of bone
-
Ralston SH. Pathogenesis of Paget's disease of bone. Bone 2008;43:819-25.
-
(2008)
Bone
, vol.43
, pp. 819-825
-
-
Ralston, S.H.1
-
4
-
-
33846516300
-
Is the prevalence of Paget's disease of bone decreasing?
-
Cundy T. Is the prevalence of Paget's disease of bone decreasing? J Bone Miner Res 2006;21(Suppl 2):9-13.
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
, pp. 9-13
-
-
Cundy, T.1
-
5
-
-
70350774165
-
Paget's disease of bone e becoming a rarity?
-
Bastin S, Bird H, Gamble G, et al. Paget's disease of bone e becoming a rarity? Rheumatology (Oxford) 2009;48:1232-5.
-
(2009)
Rheumatology (Oxford)
, vol.48
, pp. 1232-1235
-
-
Bastin, S.1
Bird, H.2
Gamble, G.3
-
7
-
-
56049117643
-
A SQSTM1/p62 mutation linked to Paget's disease increases the osteoclastogenic potential of the bone microenvironment
-
Hiruma Y, Kurihara N, Subler MA, et al. A SQSTM1/p62 mutation linked to Paget's disease increases the osteoclastogenic potential of the bone microenvironment. Hum Mol Genet 2008;17:3708-19.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3708-3719
-
-
Hiruma, Y.1
Kurihara, N.2
Subler, M.A.3
-
8
-
-
58149092378
-
Paget's disease of bone: Histologic analysis of 754 patients
-
Seitz S, Priemel M, Zustin J, et al. Paget's disease of bone: histologic analysis of 754 patients. J Bone Miner Res 2009;24:62-9.
-
(2009)
J Bone Miner Res
, vol.24
, pp. 62-69
-
-
Seitz, S.1
Priemel, M.2
Zustin, J.3
-
9
-
-
34848912628
-
The molecular pathogenesis of Paget disease of bone
-
Layfield R. The molecular pathogenesis of Paget disease of bone. Expert Rev Mol Med 2007;9:1-13.
-
(2007)
Expert Rev Mol Med
, vol.9
, pp. 1-13
-
-
Layfield, R.1
-
10
-
-
38449085976
-
Ubiquitin-mediated signalling and Paget's disease of bone
-
Layfield R, Shaw B. Ubiquitin-mediated signalling and Paget's disease of bone. BMC Biochem 2007;8(Suppl 1):S5.
-
(2007)
BMC Biochem
, vol.8
, Issue.SUPPL. 1
-
-
Layfield, R.1
Shaw, B.2
-
12
-
-
15344339092
-
Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations
-
Cavey JR, Ralston SH, Hocking LJ, et al. Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations. J Bone Miner Res 2005;20:619-24.
-
(2005)
J Bone Miner Res
, vol.20
, pp. 619-624
-
-
Cavey, J.R.1
Ralston, S.H.2
Hocking, L.J.3
-
13
-
-
33646597289
-
Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of bone
-
Cavey JR, Ralston SH, Sheppard PW, et al. Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of bone. Calcif Tissue Int 2006;78:271-7.
-
(2006)
Calcif Tissue Int
, vol.78
, pp. 271-277
-
-
Cavey, J.R.1
Ralston, S.H.2
Sheppard, P.W.3
-
14
-
-
43049108052
-
Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States
-
Rhodes EC, Johnson-Pais TL, Singer FR, et al. Sequestosome 1 (SQSTM1) mutations in Paget's disease of bone from the United States. Calcif Tissue Int 2008;82:271-7.
-
(2008)
Calcif Tissue Int
, vol.82
, pp. 271-277
-
-
Rhodes, E.C.1
Johnson-Pais, T.L.2
Singer, F.R.3
-
15
-
-
50949105285
-
Founder effect in different European countries for the recurrent P392L SQSTM1 mutation in Paget's Disease of Bone
-
Chung PY, Beyens G, Guañabens N, et al. Founder effect in different European countries for the recurrent P392L SQSTM1 mutation in Paget's Disease of Bone. Calcif Tissue Int 2008;83:34-42.
-
(2008)
Calcif Tissue Int
, vol.83
, pp. 34-42
-
-
Chung, P.Y.1
Beyens, G.2
Guañabens, N.3
-
16
-
-
19944434345
-
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, et al. Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent. J Bone Miner Res 2005;20:227-31.
-
(2005)
J Bone Miner Res
, vol.20
, pp. 227-231
-
-
Lucas, G.J.1
Hocking, L.J.2
Daroszewska, A.3
-
17
-
-
58149280230
-
Genetic epidemiology of Paget's disease of bone in Italy: Sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone
-
Falchetti A, Di Stefano M, Marini F, et al. Genetic epidemiology of Paget's disease of bone in Italy: sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone. Calcif Tissue Int 2009;84:20-37.
-
(2009)
Calcif Tissue Int
, vol.84
, pp. 20-37
-
-
Falchetti, A.1
Di Stefano, M.2
Marini, F.3
-
18
-
-
4544371010
-
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, et al. Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences. J Bone Miner Res 2004;19:1122-7.
-
(2004)
J Bone Miner Res
, vol.19
, pp. 1122-1127
-
-
Hocking, L.J.1
Lucas, G.J.2
Daroszewska, A.3
-
19
-
-
65549140668
-
Characterization of a non-UBA domain missense mutation of sequestosome 1 (SQSTM1) in Paget's disease of bone
-
Najat D, Garner T, Hagen T, et al. Characterization of a non-UBA domain missense mutation of sequestosome 1 (SQSTM1) in Paget's disease of bone. J Bone Miner Res 2009;24:632-42.
-
(2009)
J Bone Miner Res
, vol.24
, pp. 632-642
-
-
Najat, D.1
Garner, T.2
Hagen, T.3
-
20
-
-
70349101680
-
Sequestosome 1 mutations in Paget's disease of bone in Australia: Prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding
-
Rea SL, Walsh JP, Ward L, et al. Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding. J Bone Miner Res 2009;24:1216-23.
-
(2009)
J Bone Miner Res
, vol.24
, pp. 1216-1223
-
-
Rea, S.L.1
Walsh, J.P.2
Ward, L.3
-
21
-
-
61849097834
-
Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone
-
Merchant A, Smielewska M, Patel N, et al. Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone. J Bone Miner Res 2009;24:484-94.
-
(2009)
J Bone Miner Res
, vol.24
, pp. 484-494
-
-
Merchant, A.1
Smielewska, M.2
Patel, N.3
-
22
-
-
59749096578
-
Absence of somatic SQSTM1 mutations in Paget's disease of bone
-
Matthews BG, Naot D, Bava U, et al. Absence of somatic SQSTM1 mutations in Paget's disease of bone. J Clin Endocrinol Metab 2009;94:691-4.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 691-694
-
-
Matthews, B.G.1
Naot, D.2
Bava, U.3
-
23
-
-
37549034220
-
Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent
-
Lucas GJ, Riches PL, Hocking LJ, et al. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent. J Bone Miner Res 2008;23:58-63.
-
(2008)
J Bone Miner Res
, vol.23
, pp. 58-63
-
-
Lucas, G.J.1
Riches, P.L.2
Hocking, L.J.3
-
24
-
-
70450090282
-
Identification of novel genetic variants that predispose to Paget's disease of bone by genome wide association
-
Albagha OME, Visconti MR, Alonso N, et al. Identification of novel genetic variants that predispose to Paget's disease of bone by genome wide association. Bone 2009;44(Suppl 2):224-5.
-
(2009)
Bone
, vol.44
, Issue.SUPPL. 2
, pp. 224-225
-
-
Albagha, O.M.E.1
Visconti, M.R.2
Alonso, N.3
-
25
-
-
42049109083
-
Failure to detect measles virus ribonucleic acid in bone cells from patients with Paget's disease
-
Matthews BG, Afzal MA, Minor PD, et al. Failure to detect measles virus ribonucleic acid in bone cells from patients with Paget's disease. J Clin Endocrinol Metab 2008;93:398-401.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 398-401
-
-
Matthews, B.G.1
Afzal, M.A.2
Minor, P.D.3
-
26
-
-
0442325388
-
The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis
-
Durán A, Serrano M, Leitges M, et al. The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis. Dev Cell 2004;6:303-9.
-
(2004)
Dev Cell
, vol.6
, pp. 303-309
-
-
Durán, A.1
Serrano, M.2
Leitges, M.3
-
27
-
-
70349764552
-
The p62 P392L mutation linked to Paget's disease induces activation of human osteoclasts
-
Chamoux E, Couture J, Bisson M, et al. The p62 P392L mutation linked to Paget's disease induces activation of human osteoclasts. Mol Endocrinol 2009;23:1668-80.
-
(2009)
Mol Endocrinol
, vol.23
, pp. 1668-1680
-
-
Chamoux, E.1
Couture, J.2
Bisson, M.3
-
28
-
-
27444433045
-
The p62 scaffold regulates nerve growth factor-induced NF-kappaB activation by influencing TRAF6 polyubiquitination
-
Wooten MW, Geetha T, Seibenhener ML, et al. The p62 scaffold regulates nerve growth factor-induced NF-kappaB activation by influencing TRAF6 polyubiquitination. J Biol Chem 2005;280:35625- 9.
-
(2005)
J Biol Chem
, vol.280
, pp. 35625-35629
-
-
Wooten, M.W.1
Geetha, T.2
Seibenhener, M.L.3
-
29
-
-
33747624440
-
The signaling adapter p62 is an important mediator of T helper 2 cell function and allergic airway inflammation
-
Martin P, Diaz-Meco MT, Moscat J. The signaling adapter p62 is an important mediator of T helper 2 cell function and allergic airway inflammation. EMBO J 2006;25:3524-33.
-
(2006)
EMBO J
, vol.25
, pp. 3524-3533
-
-
Martin, P.1
Diaz-Meco, M.T.2
Moscat, J.3
-
30
-
-
43049124129
-
Deubiquitinating enzyme CYLD negatively regulates RANK signaling and osteoclastogenesis in mice
-
Jin W, Chang M, Paul EM, et al. Deubiquitinating enzyme CYLD negatively regulates RANK signaling and osteoclastogenesis in mice. J Clin Invest 2008;118:1858-66.
-
(2008)
J Clin Invest
, vol.118
, pp. 1858-1866
-
-
Jin, W.1
Chang, M.2
Paul, E.M.3
-
31
-
-
84856073856
-
Functional Role of p62 (SQSTM1) interaction with deubiquitinating enzyme CYLD in Paget's disease of bone
-
accessed 5 October 2009
-
Sundaram K, Shanmugarajan S, Sudhaker Rao D, et al. Functional Role of p62 (SQSTM1) interaction with deubiquitinating enzyme CYLD in Paget's disease of bone. J Bone Miner Res 2009;24(Suppl 1). http://www.asbmr.org/Meetings/AnnualMeeting/AbstractDetail.aspx?aid= 4746eb24-7fa9-4945-8a0b-cb2d2a6a6e26 (accessed 5 October 2009).
-
(2009)
J Bone Miner Res
, vol.24
, Issue.SUPPL. 1
-
-
Sundaram, K.1
Shanmugarajan, S.2
Sudhaker Rao, D.3
-
32
-
-
38549119003
-
Gene expression profiling in Paget's disease of bone: Upregulation of interferon signalling pathways in pagetic monocytes and lymphocytes
-
Nagy ZB, Gergely P, Donáth J, et al. Gene expression profiling in Paget's disease of bone: upregulation of interferon signalling pathways in pagetic monocytes and lymphocytes. J Bone Miner Res 2008;23:253-9.
-
(2008)
J Bone Miner Res
, vol.23
, pp. 253-259
-
-
Nagy, Z.B.1
Gergely, P.2
Donáth, J.3
-
33
-
-
33846505388
-
Differential gene expression in cultured osteoblasts and bone marrow stromal cells from patients with Paget's disease of bone
-
Naot D, Bava U, Matthews B, et al. Differential gene expression in cultured osteoblasts and bone marrow stromal cells from patients with Paget's disease of bone. J Bone Miner Res 2007;22:298-309.
-
(2007)
J Bone Miner Res
, vol.22
, pp. 298-309
-
-
Naot, D.1
Bava, U.2
Matthews, B.3
-
34
-
-
67349108375
-
Increased circulating Dickkopf-1 in Paget's disease of bone
-
Marshall MJ, Evans SF, Sharp CA, et al. Increased circulating Dickkopf-1 in Paget's disease of bone. Clin Biochem 2009;42:965-9.
-
(2009)
Clin Biochem
, vol.42
, pp. 965-969
-
-
Marshall, M.J.1
Evans, S.F.2
Sharp, C.A.3
-
35
-
-
52649121942
-
The N-terminus and Phe52 residue of LC3 recruit p62/SQSTM1 into autophagosomes
-
Shvets E, Fass E, Scherz-Shouval R, et al. The N-terminus and Phe52 residue of LC3 recruit p62/SQSTM1 into autophagosomes. J Cell Sci 2008;121:2685-95.
-
(2008)
J Cell Sci
, vol.121
, pp. 2685-2695
-
-
Shvets, E.1
Fass, E.2
Scherz-Shouval, R.3
-
36
-
-
58549084167
-
Ubiquitin signals autophagic degradation of cytosolic proteins and peroxisomes
-
Kim PK, Hailey DW, Mullen RT, et al. Ubiquitin signals autophagic degradation of cytosolic proteins and peroxisomes. Proc Natl Acad Sci U S A 2008;105:20567-74.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 20567-20574
-
-
Kim, P.K.1
Hailey, D.W.2
Mullen, R.T.3
-
37
-
-
65549142204
-
A role for ubiquitin in selective autophagy
-
Kirkin V, McEwan DG, Novak I, et al. A role for ubiquitin in selective autophagy. Mol Cell 2009;34:259-69.
-
(2009)
Mol Cell
, vol.34
, pp. 259-269
-
-
Kirkin, V.1
McEwan, D.G.2
Novak, I.3
-
38
-
-
58149344946
-
Midbody ring disposal by autophagy is a post-abscission event of cytokinesis
-
Pohl C, Jentsch S. Midbody ring disposal by autophagy is a post-abscission event of cytokinesis. Nat Cell Biol 2009;11:65-70.
-
(2009)
Nat Cell Biol
, vol.11
, pp. 65-70
-
-
Pohl, C.1
Jentsch, S.2
-
39
-
-
66449099090
-
Autophagy suppresses tumorigenesis through elimination of p62
-
Mathew R, Karp CM, Beaudoin B, et al. Autophagy suppresses tumorigenesis through elimination of p62. Cell 2009;137:1062-75.
-
(2009)
Cell
, vol.137
, pp. 1062-1075
-
-
Mathew, R.1
Karp, C.M.2
Beaudoin, B.3
-
40
-
-
59649092634
-
Hypoxia-activated autophagy accelerates degradation of SQSTM1/p62
-
Pursiheimo JP, Rantanen K, Heikkinen PT, et al. Hypoxia-activated autophagy accelerates degradation of SQSTM1/p62. Oncogene 2009;28:334-44.
-
(2009)
Oncogene
, vol.28
, pp. 334-344
-
-
Pursiheimo, J.P.1
Rantanen, K.2
Heikkinen, P.T.3
-
41
-
-
63449118087
-
Osteosarcoma incidence and survival rates from 1973 to 2004: Data from the Surveillance, Epidemiology, and End Results Program
-
Mirabello L, Troisi RJ, Savage SA. Osteosarcoma incidence and survival rates from 1973 to 2004: data from the Surveillance, Epidemiology, and End Results Program. Cancer 2009;115:1531-43.
-
(2009)
Cancer
, vol.115
, pp. 1531-1543
-
-
Mirabello, L.1
Troisi, R.J.2
Savage, S.A.3
-
42
-
-
38949108670
-
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
-
Klionsky DJ, Abeliovich H, Agostinis P, et al. Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy 2008;4:51-75.
-
(2008)
Autophagy
, vol.4
, pp. 51-75
-
-
Klionsky, D.J.1
Abeliovich, H.2
Agostinis, P.3
-
43
-
-
33846479861
-
Paget's disease of bone in the French population: Novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations
-
Collet C, Michou L, Audran M, et al. Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations. J Bone Miner Res 2007;22:310-7.
-
(2007)
J Bone Miner Res
, vol.22
, pp. 310-317
-
-
Collet, C.1
Michou, L.2
Audran, M.3
-
44
-
-
39849109338
-
Autophagy fights disease through cellular self-digestion
-
Mizushima N, Levine B, Cuervo AM, et al. Autophagy fights disease through cellular self-digestion. Nature 2008;451:1069-75.
-
(2008)
Nature
, vol.451
, pp. 1069-1075
-
-
Mizushima, N.1
Levine, B.2
Cuervo, A.M.3
-
45
-
-
22144466919
-
Activation of IKK by thymosin alpha1 requires the TRAF6 signalling pathway
-
Zhang P, Chan J, Dragoi AM, et al. Activation of IKK by thymosin alpha1 requires the TRAF6 signalling pathway. EMBO Rep 2005;6:531-7.
-
(2005)
EMBO Rep
, vol.6
, pp. 531-537
-
-
Zhang, P.1
Chan, J.2
Dragoi, A.M.3
-
46
-
-
60549093730
-
Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates
-
Korolchuk VI, Mansilla A, Menzies FM, et al. Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates. Mol Cell 2009;33:517-27.
-
(2009)
Mol Cell
, vol.33
, pp. 517-527
-
-
Korolchuk, V.I.1
Mansilla, A.2
Menzies, F.M.3
-
47
-
-
65549085701
-
Cullin3-based polyubiquitination and p62-dependent aggregation of caspase-8 mediate extrinsic apoptosis signaling
-
Jin Z, Li Y, Pitti R, et al. Cullin3-based polyubiquitination and p62-dependent aggregation of caspase-8 mediate extrinsic apoptosis signaling. Cell 2009;137:721-35.
-
(2009)
Cell
, vol.137
, pp. 721-735
-
-
Jin, Z.1
Li, Y.2
Pitti, R.3
-
48
-
-
33846009075
-
Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease
-
Kurihara N, Hiruma Y, Zhou H, et al. Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease. J Clin Invest 2007;117:133-42.
-
(2007)
J Clin Invest
, vol.117
, pp. 133-142
-
-
Kurihara, N.1
Hiruma, Y.2
Zhou, H.3
-
49
-
-
70449962436
-
Knock-in of the P392L mutation of SQSTM1 causes a phenotype similar to Paget's disease in mice
-
Daroszewska A, Rojas J, Rose L, et al. Knock-in of the P392L mutation of SQSTM1 causes a phenotype similar to Paget's disease in mice. Calcif Tissue Int 2008;82:S34-5.
-
(2008)
Calcif Tissue Int
, vol.82
-
-
Daroszewska, A.1
Rojas, J.2
Rose, L.3
-
50
-
-
77749307140
-
The P392L mutation of SQSTM1 causes a Paget's disease-like phenotype in mice
-
accessed 5 October 2009
-
Daroszewska A, Van't Hof R, Rose L, et al. The P392L mutation of SQSTM1 causes a Paget's disease-like phenotype in mice. J Bone Miner Res 2009;24(Suppl 1). http://www.asbmr.org/Meetings/ AnnualMeeting/AbstractDetail.aspx?aid=95738926-f13a-4dfc-af95-b58f6759122e (accessed 5 October 2009).
-
(2009)
J Bone Miner Res
, vol.24
, Issue.SUPPL. 1
-
-
Daroszewska, A.1
Van't Hof, R.2
Rose, L.3
-
51
-
-
77749311549
-
-
Daroszewska A, Rose L, Rose K, et al. Development of a novel animal model for the syndrome of inclusion body myopathy, Paget's disease and fronto-temporal dementia. Abstract OP27 presented at ECTS 36th Symposium on Calcified Tissues, Vienna, May 2009. 〈http://abstract.mci-group.com/cgi- bin/mc/printabs.pl?APP=ECTS2009-abstract&TEMPLATE=&keyf= 0497&showHide=show&client=〉. (accessed 5 October 2009).
-
Daroszewska A, Rose L, Rose K, et al. Development of a novel animal model for the syndrome of inclusion body myopathy, Paget's disease and fronto-temporal dementia. Abstract OP27 presented at ECTS 36th Symposium on Calcified Tissues, Vienna, May 2009. 〈http://abstract.mci-group.com/cgi- bin/mc/printabs.pl?APP=ECTS2009-abstract&TEMPLATE=&keyf= 0497&showHide=show&client=〉. (accessed 5 October 2009).
-
-
-
-
52
-
-
69449103157
-
Viruses and arrested autophagosome development
-
Taylor MP, Jackson WT. Viruses and arrested autophagosome development. Autophagy 2009;5:870-1.
-
(2009)
Autophagy
, vol.5
, pp. 870-871
-
-
Taylor, M.P.1
Jackson, W.T.2
-
53
-
-
0031555892
-
Low micromolar levels of hydrogen peroxide and proteasome inhibitors induce the 60-kDa A170 stress protein in murine peritoneal macrophages
-
Ishii T, Yanagawa T, Yuki K, et al. Low micromolar levels of hydrogen peroxide and proteasome inhibitors induce the 60-kDa A170 stress protein in murine peritoneal macrophages. Biochem Biophys Res Commun 1997;232:33-7.
-
(1997)
Biochem Biophys Res Commun
, vol.232
, pp. 33-37
-
-
Ishii, T.1
Yanagawa, T.2
Yuki, K.3
-
54
-
-
46749127771
-
Pathogenesis and management of Paget's disease of bone
-
Ralston SH, Langston AL, Reid IR. Pathogenesis and management of Paget's disease of bone. Lancet 2008;372:155-63.
-
(2008)
Lancet
, vol.372
, pp. 155-163
-
-
Ralston, S.H.1
Langston, A.L.2
Reid, I.R.3
-
55
-
-
77953424429
-
Randomised trial of intensive bisphosphonate treatment versus symptomatic management in Paget's disease of bone
-
Published Online First: 6 July, doi:10.1359/jbmr.090709
-
Langston AL, Campbell MK, Fraser WD, et al. Randomised trial of intensive bisphosphonate treatment versus symptomatic management in Paget's disease of bone. J Bone Miner Res Published Online First: 6 July 2009. doi:10.1359/jbmr.090709.
-
(2009)
J Bone Miner Res
-
-
Langston, A.L.1
Campbell, M.K.2
Fraser, W.D.3
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