-
1
-
-
0002640802
-
On a form of chronic inflammation of bones (osteitis deformans)
-
Paget SJ: On a form of chronic inflammation of bones (osteitis deformans). Med Chir Trans 1877, 60:37-64.9.
-
(1877)
Med Chir Trans
, vol.60
-
-
Paget, S.J.1
-
2
-
-
0013477519
-
Paget's disease of bone: Clinical and metabolic observations
-
NagantdedeuxchaisneC C, Krane SM: Paget's disease of bone: clinical and metabolic observations. Medicine 1964, 43:233-266.
-
(1964)
Medicine
, vol.43
, pp. 233-266
-
-
Nagantdedeuxchaisnes, C.1
Krane, S.M.2
-
3
-
-
0042860352
-
Ueber ostitis deformans Paget
-
Schmorl G: Ueber ostitis deformans Paget. Virchows Arch Pathol Anat 1932, 283:694-751.
-
(1932)
Virchows Arch Pathol Anat
, vol.283
, pp. 694-751
-
-
Schmorl, G.1
-
4
-
-
0007512539
-
Angioid streaks and osteitis deformans
-
Terry TL: Angioid streaks and osteitis deformans. Trans Am Ophthalmol Soc 1934, 32:555-573.
-
(1934)
Trans Am Ophthalmol Soc
, vol.32
, pp. 555-573
-
-
Terry, T.L.1
-
5
-
-
49749190582
-
Paget's disease of bone; incidence and subclinical forms
-
Collins DH: Paget's disease of bone; incidence and subclinical forms. Lancet 1956, 271:51-57.
-
(1956)
Lancet
, vol.271
, pp. 51-57
-
-
Collins, D.H.1
-
6
-
-
0016264708
-
Distribution of Paget's disease in England, Wales and Scotland and a possible relationship with vitamin D deficiency in childhood
-
Barker DJ, Gardner MJ: Distribution of Paget's disease in England, Wales and Scotland and a possible relationship with vitamin D deficiency in childhood. Br J Prev Soc Med 1974, 28:226-232.
-
(1974)
Br J Prev Soc Med
, vol.28
, pp. 226-232
-
-
Barker, D.J.1
Gardner, M.J.2
-
7
-
-
0014503906
-
Geographic variation in the prevalence of Paget's disease of bone
-
Rosenbaum HD, Hanson DJ: Geographic variation in the prevalence of Paget's disease of bone. Radiology 1969, 92:959-963.
-
(1969)
Radiology
, vol.92
, pp. 959-963
-
-
Rosenbaum, H.D.1
Hanson, D.J.2
-
8
-
-
0034094376
-
Prevalence of pelvic Paget's disease of bone in the United States
-
Altman RD, Bloch DA, Hochberg MC, Murphy WA: Prevalence of pelvic Paget's disease of bone in the United States. J Bone Miner Res 2000, 15:461-465.
-
(2000)
J Bone Miner Res
, vol.15
, pp. 461-465
-
-
Altman, R.D.1
Bloch, D.A.2
Hochberg, M.C.3
Murphy, W.A.4
-
9
-
-
0033827275
-
Long-term trends in the incidence of Paget's disease of bone
-
Tiegs RD, Lohse CM, Wollan PC, Melton LJ: Long-term trends in the incidence of Paget's disease of bone. Bone 2000, 27:423-427.
-
(2000)
Bone
, vol.27
, pp. 423-427
-
-
Tiegs, R.D.1
Lohse, C.M.2
Wollan, P.C.3
Melton, L.J.4
-
10
-
-
0032954603
-
The epidemiology of Paget's disease in Britain: Is the prevalence decreasing?
-
Cooper C, Schafheutle K, Dennison E, et al.: The epidemiology of Paget's disease in Britain: Is the prevalence decreasing? J Bone Miner Res 1999, 14:192-197.
-
(1999)
J Bone Miner Res
, vol.14
, pp. 192-197
-
-
Cooper, C.1
Schafheutle, K.2
Dennison, E.3
-
11
-
-
0036861114
-
Paget's disease in New Zealand: Evidence for declining prevalence
-
Doyle T, Gunn J, Anderson G, et al.: Paget's disease in New Zealand: evidence for declining prevalence. Bone 2002, 31:616-619.
-
(2002)
Bone
, vol.31
, pp. 616-619
-
-
Doyle, T.1
Gunn, J.2
Anderson, G.3
-
12
-
-
0036169378
-
Is clinical expressiveness of Paget's disease of bone decreasing?
-
Morales-Piga AA, Bachiller-Corral FJ, Abraira V, et al.: Is clinical expressiveness of Paget's disease of bone decreasing? Bone 2002, 30:399-403.
-
(2002)
Bone
, vol.30
, pp. 399-403
-
-
Morales-Piga, A.A.1
Bachiller-Corral, F.J.2
Abraira, V.3
-
13
-
-
11944270643
-
Paget's disease of bone in New Zealand: Continued decline in disease severity
-
Cundy HR, Gamble G, Wattie D, et al.: Paget's disease of bone in New Zealand: Continued decline in disease severity. Calcif Tissue Int 2004, 75:358-364.
-
(2004)
Calcif Tissue Int
, vol.75
, pp. 358-364
-
-
Cundy, H.R.1
Gamble, G.2
Wattie, D.3
-
14
-
-
33749250010
-
Epidemiology of Paget's disease in Europe: The prevalence is decreasing
-
Poor G, Donath J, Fornet B, Cooper C: Epidemiology of Paget's disease in Europe: The prevalence is decreasing. J Bone Miner Res 2006, 21:1545-1549.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1545-1549
-
-
Poor, G.1
Donath, J.2
Fornet, B.3
Cooper, C.4
-
15
-
-
34548306762
-
Effect of age and gender on the number and distribution of sites in Paget's disease of bone
-
Haddaway MJ, Davie MW, McCall IW, Howdle S: Effect of age and gender on the number and distribution of sites in Paget's disease of bone. Br J Radiol 2007, 80:532-536.
-
(2007)
Br J Radiol
, vol.80
, pp. 532-536
-
-
Haddaway, M.J.1
Davie, M.W.2
McCall, I.W.3
Howdle, S.4
-
16
-
-
25444484930
-
Prevalence of Paget's disease of bone in Italy
-
Gennari L, Di Stefano M, Merlotti D, et al.: Prevalence of Paget's disease of bone in Italy. J Bone Miner Res 2005, 20:1845-1850.
-
(2005)
J Bone Miner Res
, vol.20
, pp. 1845-1850
-
-
Gennari, L.1
Di Stefano, M.2
Merlotti, D.3
-
17
-
-
33845225616
-
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, et al.: Evidence for increased clinical severity of familial and sporadic Paget's disease of bone in Campania, southern Italy. J Bone Miner Res 2006, 21:1828-1835.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1828-1835
-
-
Rendina, D.1
Gennari, L.2
De Filippo, G.3
-
18
-
-
0025875602
-
Familial aggregation of Paget's disease of bone
-
Siris ES, Ottman R, Flaster E, Kelsey JL: Familial aggregation of Paget's disease of bone. J Bone Miner Res 1991, 6:495-500.
-
(1991)
J Bone Miner Res
, vol.6
, pp. 495-500
-
-
Siris, E.S.1
Ottman, R.2
Flaster, E.3
Kelsey, J.L.4
-
19
-
-
2142706743
-
Analysis of environmental factors in familial versus sporadic Paget's disease of bone - The New England Registry for Paget's Disease of Bone
-
Seton M, Choi HK, Hansen MF, et al.: Analysis of environmental factors in familial versus sporadic Paget's disease of bone - the New England Registry for Paget's Disease of Bone. J Bone Miner Res 2003, 18:1519-1524.
-
(2003)
J Bone Miner Res
, vol.18
, pp. 1519-1524
-
-
Seton, M.1
Choi, H.K.2
Hansen, M.F.3
-
20
-
-
0036094026
-
Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone
-
Laurin N, Brown JP, Morissette J, Raymond V: Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone. Am J Hum Genet 2002, 70:1582-1588.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1582-1588
-
-
Laurin, N.1
Brown, J.P.2
Morissette, J.3
Raymond, V.4
-
21
-
-
34247861003
-
Sequestosome 1: Mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone
-
MorissetteMJ, Laurin N, Brown JP: Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone. J Bone Miner Res 2006, 21(Suppl 2):P38-P44.
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
-
-
Morissette, J.1
Laurin, N.2
Brown, J.P.3
-
22
-
-
34247188567
-
Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations
-
Bolland MJ, Tong PC, Naot D, et al.: Delayed development of Paget's disease in offspring inheriting SQSTM1 mutations. J Bone Miner Res 2007, 22:411-415.
-
(2007)
J Bone Miner Res
, vol.22
, pp. 411-415
-
-
Bolland, M.J.1
Tong, P.C.2
Naot, D.3
-
23
-
-
2942709744
-
Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees
-
Good DA, Busfield F, Fletcher BH, et al.: Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees. Bone 2004, 35:277-282.
-
(2004)
Bone
, vol.35
, pp. 277-282
-
-
Good, D.A.1
Busfield, F.2
Fletcher, B.H.3
-
24
-
-
4444335629
-
Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease
-
Beyens G, Van Hul E, Van Driessche K, et al.: Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease. Calcif Tissue Int 2004, 75:144-152.
-
(2004)
Calcif Tissue Int
, vol.75
, pp. 144-152
-
-
Beyens, G.1
Van Hul, E.2
Van Driessche, K.3
-
25
-
-
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, 82:271-277.
-
(2008)
Calcif Tissue Int
, vol.82
, pp. 271-277
-
-
Rhodes, E.C.1
Johnson-Pais, T.L.2
Singer, F.R.3
-
26
-
-
19944434345
-
Ubiquitinassociated 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.: Ubiquitinassociated 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, 20:227-231.
-
(2005)
J Bone Miner Res
, vol.20
, pp. 227-231
-
-
Lucas, G.J.1
Hocking, L.J.2
Daroszewska, A.3
-
27
-
-
50949105285
-
Founder effect in different European countries for the recurrent P392L SQSTM1 mutation in Paget's disease of bone
-
Chung PY, Beyens G, Guanabens 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
Guanabens, N.3
-
28
-
-
41949134141
-
Ubiquitin recognition by the ubiquitin-associated domain of p62 involves a novel conformational switch
-
Long J, Gallagher TR, Cavey JR, et al.: Ubiquitin recognition by the ubiquitin-associated domain of p62 involves a novel conformational switch. J Biol Chem 2008, 283:5427-5440.
-
(2008)
J Biol Chem
, vol.283
, pp. 5427-5440
-
-
Long, J.1
Gallagher, T.R.2
Cavey, J.R.3
-
29
-
-
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, 19:1122-1127.
-
(2004)
J Bone Miner Res
, vol.19
, pp. 1122-1127
-
-
Hocking, L.J.1
Lucas, G.J.2
Daroszewska, A.3
-
30
-
-
2342493320
-
Familial Paget's disease in The Netherlands: Occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations
-
Eekhoff EW, Karperien M, Houtsma D, et al.: Familial Paget's disease in The Netherlands: Occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations. Arthritis Rheum 2004, 50:1650-1654.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 1650-1654
-
-
Eekhoff, E.W.1
Karperien, M.2
Houtsma, D.3
-
31
-
-
33745510646
-
A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype
-
Rea SL, Walsh JP, Ward L, et al.: A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype. J Bone Miner Res 2006, 21:1136-1145.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1136-1145
-
-
Rea, S.L.1
Walsh, J.P.2
Ward, L.3
-
32
-
-
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, 22:310-317.
-
(2007)
J Bone Miner Res
, vol.22
, pp. 310-317
-
-
Collet, C.1
Michou, L.2
Audran, M.3
-
33
-
-
0037070216
-
Structure and functional properties of the ubiquitin binding protein p62
-
Geetha T, Wooten MW: Structure and functional properties of the ubiquitin binding protein p62. FEBS Lett 2002, 512:19-24.
-
(2002)
FEBS Lett
, vol.512
, pp. 19-24
-
-
Geetha, T.1
Wooten, M.W.2
-
34
-
-
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
-
35
-
-
0442325388
-
The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis
-
Duran A, Serrano M, Leitges M, et al.: The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis. Dev Cell 2004, 6:303-309.
-
(2004)
Dev Cell
, vol.6
, pp. 303-309
-
-
Duran, A.1
Serrano, M.2
Leitges, M.3
-
36
-
-
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, 117:133-142.
-
(2007)
J Clin Invest
, vol.117
, pp. 133-142
-
-
Kurihara, N.1
Hiruma, Y.2
Zhou, H.3
-
37
-
-
0019756680
-
Towards a viral etiology for Paget's disease of bone
-
Rebel A, Basle M, Pouplard A, et al.: Towards a viral etiology for Paget's disease of bone. Metab Bone Dis Relat Res 1981, 3:235-238.
-
(1981)
Metab Bone Dis Relat Res
, vol.3
, pp. 235-238
-
-
Rebel, A.1
Basle, M.2
Pouplard, A.3
-
38
-
-
0018962390
-
Cell cultures from bone affected by Paget's disease
-
Mills BG, Singer FR, Weiner LP, Holst PA: Cell cultures from bone affected by Paget's disease. Arthritis Rheum 1980, 23:1115-1120.
-
(1980)
Arthritis Rheum
, vol.23
, pp. 1115-1120
-
-
Mills, B.G.1
Singer, F.R.2
Weiner, L.P.3
Holst, P.A.4
-
39
-
-
0032146198
-
Detection of canine distemper virus in 100% of Paget's disease samples by in situ-reverse transcriptase-polymerase chain reaction
-
Mee AP, Dixon JA, Hoyland JA, et al.: Detection of canine distemper virus in 100% of Paget's disease samples by in situ-reverse transcriptase-polymerase chain reaction. Bone 1998, 23:171-175.
-
(1998)
Bone
, vol.23
, pp. 171-175
-
-
Mee, A.P.1
Dixon, J.A.2
Hoyland, J.A.3
-
40
-
-
0032883330
-
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone
-
Reddy SV, Menaa C, Singer FR, et al.: Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone. Exp Hematol 1999, 27:1528-1532.
-
(1999)
Exp Hematol
, vol.27
, pp. 1528-1532
-
-
Reddy, S.V.1
Menaa, C.2
Singer, F.R.3
-
41
-
-
0029003364
-
Bone marrow mononuclear cells from patients with Paget's disease contain measles virus nucleocapsid messenger ribonucleic acid that has mutations in a specific region of the sequence
-
Reddy SV, Singer FR, Roodman GD: Bone marrow mononuclear cells from patients with Paget's disease contain measles virus nucleocapsid messenger ribonucleic acid that has mutations in a specific region of the sequence. J Clin Endocrinol Metab 1995, 80:2108-2111.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2108-2111
-
-
Reddy, S.V.1
Singer, F.R.2
Roodman, G.D.3
-
42
-
-
0029842505
-
Paget's disease of bone and unvaccinated dogs
-
Khan SA, Brennan P, Newman J, et al.: Paget's disease of bone and unvaccinated dogs. Bone 1996, 19:47-50.
-
(1996)
Bone
, vol.19
, pp. 47-50
-
-
Khan, S.A.1
Brennan, P.2
Newman, J.3
-
43
-
-
34247848056
-
Experimental models of Paget's disease
-
Kurihara N, Zhou H, Reddy SV, et al.: Experimental models of Paget's disease. J Bone Miner Res 2006, 21(Suppl 2):P55-P57.
-
(2006)
J Bone Miner Res
, vol.21
, Issue.SUPPL. 2
-
-
Kurihara, N.1
Zhou, H.2
Reddy, S.V.3
-
44
-
-
33846433786
-
Canine distemper virus induces human osteoclastogenesis through NF-kappaB and sequestosome 1/P62 activation
-
Selby PL, Davies M, Mee AP: Canine distemper virus induces human osteoclastogenesis through NF-kappaB and sequestosome 1/P62 activation. J Bone Miner Res 2006, 21:1750-1756.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1750-1756
-
-
Selby, P.L.1
Davies, M.2
Mee, A.P.3
-
45
-
-
0033831096
-
Absence of measles virus and canine distemper virus transcripts in long-term bone marrow cultures from patients with Paget's disease of bone
-
Ooi CG, Walsh CA, Gallagher JA, Fraser WD: Absence of measles virus and canine distemper virus transcripts in long-term bone marrow cultures from patients with Paget's disease of bone. Bone 2000, 27:417-421.
-
(2000)
Bone
, vol.27
, pp. 417-421
-
-
Ooi, C.G.1
Walsh, C.A.2
Gallagher, J.A.3
Fraser, W.D.4
-
46
-
-
0033713488
-
A negative search for a paramyxoviral etiology of Paget's disease of bone: Molecular, immunological, and ultrastructural studies in UK patients
-
Helfrich MH, Hobson RP, Grabowski PS, et al.: A negative search for a paramyxoviral etiology of Paget's disease of bone: Molecular, immunological, and ultrastructural studies in UK patients. J Bone Miner Res 2000, 15:2315-2329.
-
(2000)
J Bone Miner Res
, vol.15
, pp. 2315-2329
-
-
Helfrich, M.H.1
Hobson, R.P.2
Grabowski, P.S.3
-
47
-
-
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, 93:1398-1401.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 1398-1401
-
-
Matthews, B.G.1
Afzal, M.A.2
Minor, P.D.3
-
48
-
-
42749094400
-
Genetics and aetiology of Pagetic disorders of bone
-
Helfrich MH, Hocking LJ: Genetics and aetiology of Pagetic disorders of bone. Arch Biochem Biophys 2008, 473:172-182.
-
(2008)
Arch Biochem Biophys
, vol.473
, pp. 172-182
-
-
Helfrich, M.H.1
Hocking, L.J.2
-
49
-
-
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
-
50
-
-
0033987358
-
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis
-
Hughes AE, Ralston SH, Marken J, et al.: Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis. Nat Genet 2000, 24:45-48.
-
(2000)
Nat Genet
, vol.24
, pp. 45-48
-
-
Hughes, A.E.1
Ralston, S.H.2
Marken, J.3
-
52
-
-
0036133351
-
Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis
-
Whyte MP, Hughes AE: Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis. J Bone Miner Res 2002, 17:26-29.
-
(2002)
J Bone Miner Res
, vol.17
, pp. 26-29
-
-
Whyte, M.P.1
Hughes, A.E.2
-
53
-
-
0036778369
-
Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A gene
-
Palenzuela L, Vives-Bauza C, Fernandez-Cadenas I, et al.: Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A gene. J Med Genet 2002, 39:E67.
-
(2002)
J Med Genet
, vol.39
-
-
Palenzuela, L.1
Vives-Bauza, C.2
Fernandez-Cadenas, I.3
-
54
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts GD, Wymer J, Kovach MJ, et al.: Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat Genet 2004, 36:377-381.
-
(2004)
Nat Genet
, vol.36
, pp. 377-381
-
-
Watts, G.D.1
Wymer, J.2
Kovach, M.J.3
-
55
-
-
31544436590
-
Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone
-
Lucas GJ, Mehta SG, Hocking LJ, et al.: Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone. Bone 2006, 38:280-285.
-
(2006)
Bone
, vol.38
, pp. 280-285
-
-
Lucas, G.J.1
Mehta, S.G.2
Hocking, L.J.3
-
56
-
-
34447098604
-
Valosincontaining protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy
-
Guinto JB, Ritson GP, Taylor JP, Forman MS: Valosincontaining protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy. Acta Neuropathol 2007, 114:55-61.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 55-61
-
-
Guinto, J.B.1
Ritson, G.P.2
Taylor, J.P.3
Forman, M.S.4
-
57
-
-
41949141411
-
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry
-
Pikkarainen M, Hartikainen P, Alafuzoff I: Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry. J Neuropathol Exp Neurol 2008, 67: 280-298.
-
(2008)
J Neuropathol Exp Neurol
, vol.67
, pp. 280-298
-
-
Pikkarainen, M.1
Hartikainen, P.2
Alafuzoff, I.3
|