-
1
-
-
0028258354
-
Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases
-
COI: 1:STN:280:DyaK2c3kvFertQ%3D%3D, PID: 8191875
-
Lindberg C, Persson LI, Bjorkander J, Oldfors A. Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases. Acta Neurol Scand. 1994;89(2):123–31.
-
(1994)
Acta Neurol Scand
, vol.89
, Issue.2
, pp. 123-131
-
-
Lindberg, C.1
Persson, L.I.2
Bjorkander, J.3
Oldfors, A.4
-
2
-
-
0034649445
-
Epidemiology of inclusion body myositis in the Netherlands: a nationwide study
-
COI: 1:STN:280:DC%2BD3M%2FlvFyntQ%3D%3D, PID: 11087787
-
Badrising UA, Maat-Schieman M, van Duinen SG, et al. Epidemiology of inclusion body myositis in the Netherlands: a nationwide study. Neurology. 2000;55(9):1385–7.
-
(2000)
Neurology
, vol.55
, Issue.9
, pp. 1385-1387
-
-
Badrising, U.A.1
Maat-Schieman, M.2
van Duinen, S.G.3
-
3
-
-
0029801221
-
Incidence of rare systemic rheumatic and connective tissue diseases in Finland
-
COI: 1:STN:280:DyaK28vgs1yntA%3D%3D, PID: 8810933
-
Kaipiainen-Seppanen O, Aho K. Incidence of rare systemic rheumatic and connective tissue diseases in Finland. J Intern Med. 1996;240(2):81–4.
-
(1996)
J Intern Med
, vol.240
, Issue.2
, pp. 81-84
-
-
Kaipiainen-Seppanen, O.1
Aho, K.2
-
4
-
-
0034098406
-
Prevalence of sporadic inclusion body myositis in Western Australia
-
COI: 1:STN:280:DC%2BD3czgtlShsg%3D%3D, PID: 10842277
-
Phillips BA, Zilko PJ, Mastaglia FL. Prevalence of sporadic inclusion body myositis in Western Australia. Muscle Nerve. 2000;23(6):970–2.
-
(2000)
Muscle Nerve
, vol.23
, Issue.6
, pp. 970-972
-
-
Phillips, B.A.1
Zilko, P.J.2
Mastaglia, F.L.3
-
5
-
-
0034829106
-
Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period
-
COI: 1:STN:280:DC%2BD3MrgtlWrsg%3D%3D, PID: 11552086
-
Felice KJ, North WA. Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period. Medicine. 2001;80(5):320–7.
-
(2001)
Medicine
, vol.80
, Issue.5
, pp. 320-327
-
-
Felice, K.J.1
North, W.A.2
-
6
-
-
55549128210
-
Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis
-
Needham M, Corbett A, Day T, Christiansen F, Fabian V, Mastaglia FL. Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis. J Clin Neurosci Off J Neurosurg Soc Australas. 2008;15(12):1350–3.
-
(2008)
J Clin Neurosci Off J Neurosurg Soc Australas
, vol.15
, Issue.12
, pp. 1350-1353
-
-
Needham, M.1
Corbett, A.2
Day, T.3
Christiansen, F.4
Fabian, V.5
Mastaglia, F.L.6
-
7
-
-
40649124555
-
Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota
-
PID: 18203321
-
Wilson FC, Ytterberg SR, St Sauver JL, Reed AM. Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota. J Rheumatol. 2008;35(3):445–7.
-
(2008)
J Rheumatol
, vol.35
, Issue.3
, pp. 445-447
-
-
Wilson, F.C.1
Ytterberg, S.R.2
St Sauver, J.L.3
Reed, A.M.4
-
8
-
-
79958054280
-
-
Oflazer PS, Deymeer F, Parman Y. Sporadic-inclusion body myositis (s-IBM) is not so prevalent in Istanbul/Turkey: a muscle biopsy based survey. Acta myologica: myopathies and cardiomyopathies: official journal of the Mediterranean Society of Myology/edited by the Gaetano Conte Academy for the study of striated muscle diseases 2011;30(1):34–6
-
Oflazer PS, Deymeer F, Parman Y. Sporadic-inclusion body myositis (s-IBM) is not so prevalent in Istanbul/Turkey: a muscle biopsy based survey. Acta myologica: myopathies and cardiomyopathies: official journal of the Mediterranean Society of Myology/edited by the Gaetano Conte Academy for the study of striated muscle diseases 2011;30(1):34–6.
-
-
-
-
9
-
-
84862559249
-
Increase in number of sporadic inclusion body myositis (sIBM) in Japan
-
PID: 21800140
-
Suzuki N, Aoki M, Mori-Yoshimura M, Hayashi YK, Nonaka I, Nishino I. Increase in number of sporadic inclusion body myositis (sIBM) in Japan. J Neurol. 2012;259(3):554–6.
-
(2012)
J Neurol
, vol.259
, Issue.3
, pp. 554-556
-
-
Suzuki, N.1
Aoki, M.2
Mori-Yoshimura, M.3
Hayashi, Y.K.4
Nonaka, I.5
Nishino, I.6
-
10
-
-
84896058952
-
Incidence and prevalence of idiopathic inflammatory myopathies in South Australia: a 30-year epidemiologic study of histology-proven cases
-
PID: 23981756
-
Tan JA, Roberts-Thomson PJ, Blumbergs P, Hakendorf P, Cox SR, Limaye V. Incidence and prevalence of idiopathic inflammatory myopathies in South Australia: a 30-year epidemiologic study of histology-proven cases. Int J Rheum Dis. 2013;16(3):331–8.
-
(2013)
Int J Rheum Dis
, vol.16
, Issue.3
, pp. 331-338
-
-
Tan, J.A.1
Roberts-Thomson, P.J.2
Blumbergs, P.3
Hakendorf, P.4
Cox, S.R.5
Limaye, V.6
-
11
-
-
0023252979
-
Spectrum of inclusion body myositis
-
COI: 1:STN:280:DyaL1c%2FkvV2qsA%3D%3D, PID: 2823752
-
Ringel SP, Kenny CE, Neville HE, Giorno R, Carry MR. Spectrum of inclusion body myositis. Arch Neurol. 1987;44(11):1154–7.
-
(1987)
Arch Neurol
, vol.44
, Issue.11
, pp. 1154-1157
-
-
Ringel, S.P.1
Kenny, C.E.2
Neville, H.E.3
Giorno, R.4
Carry, M.R.5
-
13
-
-
84885201889
-
Update in inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3sXhsFeltrnL, PID: 24067381
-
Machado P, Brady S, Hanna MG. Update in inclusion body myositis. Curr Opin Rheumatol. 2013;25(6):763–71.
-
(2013)
Curr Opin Rheumatol
, vol.25
, Issue.6
, pp. 763-771
-
-
Machado, P.1
Brady, S.2
Hanna, M.G.3
-
14
-
-
81055125519
-
Long-term observational study of sporadic inclusion body myositis
-
Large retrospective study describing the clinical and demographic features of IBM and progression over time
-
Benveniste O, Guiguet M, Freebody J, et al. Long-term observational study of sporadic inclusion body myositis. Brain J Neurol. 2011;134(Pt 11):3176–84. Large retrospective study describing the clinical and demographic features of IBM and progression over time.
-
(2011)
Brain J Neurol
, vol.134
, pp. 3176-3184
-
-
Benveniste, O.1
Guiguet, M.2
Freebody, J.3
-
15
-
-
84875162170
-
Update on treatment of inclusion body myositis
-
PID: 23529584
-
Breithaupt M, Schmidt J. Update on treatment of inclusion body myositis. Curr Rheumatol Rep. 2013;15(5):329.
-
(2013)
Curr Rheumatol Rep
, vol.15
, Issue.5
, pp. 329
-
-
Breithaupt, M.1
Schmidt, J.2
-
16
-
-
77958035689
-
Novel therapeutic approaches for inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3cXht1ahu7jI, PID: 20827206
-
Lloyd TE. Novel therapeutic approaches for inclusion body myositis. Curr Opin Rheumatol. 2010;22(6):658–64.
-
(2010)
Curr Opin Rheumatol
, vol.22
, Issue.6
, pp. 658-664
-
-
Lloyd, T.E.1
-
17
-
-
84902702309
-
Sporadic inclusion body myositis: the genetic contributions to the pathogenesis
-
PID: 24948216, Comprehensive review of genetic susceptibility risk factors for IBM
-
Gang Q, Bettencourt C, Machado P, Hanna MG, Houlden H. Sporadic inclusion body myositis: the genetic contributions to the pathogenesis. Orphanet J Rare Dis. 2014;9:88. Comprehensive review of genetic susceptibility risk factors for IBM.
-
(2014)
Orphanet J Rare Dis
, vol.9
, pp. 88
-
-
Gang, Q.1
Bettencourt, C.2
Machado, P.3
Hanna, M.G.4
Houlden, H.5
-
18
-
-
0032522265
-
HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies
-
COI: 1:CAS:528:DyaK1cXitlSqsro%3D, PID: 9628455
-
Koffman BM, Sivakumar K, Simonis T, Stroncek D, Dalakas MC. HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies. J Neuroimmunol. 1998;84(2):139–42.
-
(1998)
J Neuroimmunol
, vol.84
, Issue.2
, pp. 139-142
-
-
Koffman, B.M.1
Sivakumar, K.2
Simonis, T.3
Stroncek, D.4
Dalakas, M.C.5
-
19
-
-
0028072558
-
HLA associations with inclusion body myositis
-
COI: 1:STN:280:DyaK2M%2FgvVensA%3D%3D, PID: 7923882
-
Garlepp MJ, Laing B, Zilko PJ, Ollier W, Mastaglia FL. HLA associations with inclusion body myositis. Clin Exp Immunol. 1994;98(1):40–5.
-
(1994)
Clin Exp Immunol
, vol.98
, Issue.1
, pp. 40-45
-
-
Garlepp, M.J.1
Laing, B.2
Zilko, P.J.3
Ollier, W.4
Mastaglia, F.L.5
-
20
-
-
10744233697
-
Analysis of HLA class I and II alleles in sporadic inclusion-body myositis
-
PID: 14648147
-
Lampe JB, Gossrau G, Kempe A, et al. Analysis of HLA class I and II alleles in sporadic inclusion-body myositis. J Neurol. 2003;250(11):1313–7.
-
(2003)
J Neurol
, vol.250
, Issue.11
, pp. 1313-1317
-
-
Lampe, J.B.1
Gossrau, G.2
Kempe, A.3
-
21
-
-
11144270207
-
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis
-
COI: 1:CAS:528:DC%2BD2cXhtVGit77P, PID: 15623710
-
Badrising UA, Schreuder GM, Giphart MJ, et al. Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis. Neurology. 2004;63(12):2396–8.
-
(2004)
Neurology
, vol.63
, Issue.12
, pp. 2396-2398
-
-
Badrising, U.A.1
Schreuder, G.M.2
Giphart, M.J.3
-
22
-
-
8144225858
-
Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3
-
COI: 1:CAS:528:DC%2BD2cXhtVKjsrbI, PID: 15496200
-
Price P, Santoso L, Mastaglia F, et al. Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3. Tissue Antigens. 2004;64(5):575–80.
-
(2004)
Tissue Antigens
, vol.64
, Issue.5
, pp. 575-580
-
-
Price, P.1
Santoso, L.2
Mastaglia, F.3
-
23
-
-
27944432584
-
Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 allelic profiles and motifs define clinicopathologic groups in caucasians
-
PID: 16267409
-
O’Hanlon TP, Carrick DM, Arnett FC, et al. Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 allelic profiles and motifs define clinicopathologic groups in caucasians. Medicine. 2005;84(6):338–49.
-
(2005)
Medicine
, vol.84
, Issue.6
, pp. 338-349
-
-
O’Hanlon, T.P.1
Carrick, D.M.2
Arnett, F.C.3
-
24
-
-
50449098865
-
Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases
-
COI: 1:STN:280:DC%2BD1critVKhuw%3D%3D, PID: 18258695
-
Needham M, James I, Corbett A, et al. Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases. J Neurol Neurosurg Psychiatry. 2008;79(9):1056–60.
-
(2008)
J Neurol Neurosurg Psychiatry
, vol.79
, Issue.9
, pp. 1056-1060
-
-
Needham, M.1
James, I.2
Corbett, A.3
-
25
-
-
70350211088
-
Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype
-
Mastaglia FL, Needham M, Scott A, et al. Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype. Neuromuscul Dis. 2009;19(11):763–5.
-
(2009)
Neuromuscul Dis
, vol.19
, Issue.11
, pp. 763-765
-
-
Mastaglia, F.L.1
Needham, M.2
Scott, A.3
-
26
-
-
84864856565
-
High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes
-
COI: 1:CAS:528:DC%2BC38Xns1Cgsbw%3D, PID: 22633068
-
Rojana-udomsart A, James I, Castley A, et al. High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes. J Neuroimmunol. 2012;250(1–2):77–82.
-
(2012)
J Neuroimmunol
, vol.250
, Issue.1-2
, pp. 77-82
-
-
Rojana-udomsart, A.1
James, I.2
Castley, A.3
-
27
-
-
33646469854
-
Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1
-
Scott AP, Allcock RJ, Mastaglia F, Nishino I, Nonaka I, Laing N. Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1. Neuromuscul Dis. 2006;16(5):311–5.
-
(2006)
Neuromuscul Dis
, vol.16
, Issue.5
, pp. 311-315
-
-
Scott, A.P.1
Allcock, R.J.2
Mastaglia, F.3
Nishino, I.4
Nonaka, I.5
Laing, N.6
-
28
-
-
79957989574
-
Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex
-
COI: 1:CAS:528:DC%2BC3MXntFCnu70%3D, PID: 21543121
-
Scott AP, Laing NG, Mastaglia F, et al. Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex. J Neuroimmunol. 2011;235(1–2):77–83.
-
(2011)
J Neuroimmunol
, vol.235
, Issue.1-2
, pp. 77-83
-
-
Scott, A.P.1
Laing, N.G.2
Mastaglia, F.3
-
29
-
-
84864833593
-
Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis
-
COI: 1:CAS:528:DC%2BC38Xpt1Sit7g%3D, PID: 22732452
-
Scott AP, Laing NG, Mastaglia F, Dalakas M, Needham M, Allcock RJ. Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. J Neuroimmunol. 2012;250(1–2):66–70.
-
(2012)
J Neuroimmunol
, vol.250
, Issue.1-2
, pp. 66-70
-
-
Scott, A.P.1
Laing, N.G.2
Mastaglia, F.3
Dalakas, M.4
Needham, M.5
Allcock, R.J.6
-
30
-
-
84876491405
-
Autoantibodies to cytosolic 5′-nucleotidase 1A in inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3sXmt1Oju7Y%3D, PID: 23460448, Description and diagnostic performance of autoantibodies against cytosolic 5′-nucleotidase 1A in IBM
-
Pluk H, van Hoeve BJ, van Dooren SH, et al. Autoantibodies to cytosolic 5′-nucleotidase 1A in inclusion body myositis. Ann Neurol. 2013;73(3):397–407. Description and diagnostic performance of autoantibodies against cytosolic 5′-nucleotidase 1A in IBM.
-
(2013)
Ann Neurol
, vol.73
, Issue.3
, pp. 397-407
-
-
Pluk, H.1
van Hoeve, B.J.2
van Dooren, S.H.3
-
31
-
-
84876499456
-
Cytosolic 5′-nucleotidase 1A autoimmunity in sporadic inclusion body myositis
-
PID: 23596012, Description and diagnostic performance of autoantibodies against cytosolic 5′-nucleotidase 1A in IBM
-
Larman HB, Salajegheh M, Nazareno R, et al. Cytosolic 5′-nucleotidase 1A autoimmunity in sporadic inclusion body myositis. Ann Neurol. 2013;73(3):408–18. Description and diagnostic performance of autoantibodies against cytosolic 5′-nucleotidase 1A in IBM.
-
(2013)
Ann Neurol
, vol.73
, Issue.3
, pp. 408-418
-
-
Larman, H.B.1
Salajegheh, M.2
Nazareno, R.3
-
32
-
-
0027444952
-
beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositis
-
COI: 1:CAS:528:DyaK2cXitFCnsrk%3D, PID: 7692809
-
Askanas V, Alvarez RB, Engel WK. beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositis. Ann Neurol. 1993;34(4):551–60.
-
(1993)
Ann Neurol
, vol.34
, Issue.4
, pp. 551-560
-
-
Askanas, V.1
Alvarez, R.B.2
Engel, W.K.3
-
33
-
-
0029147313
-
Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy
-
COI: 1:STN:280:DyaK2Mzot1Knug%3D%3D, PID: 7654077
-
Sivakumar K, Cervenakova L, Dalakas MC, et al. Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy. Ann Neurol. 1995;38(2):267–9.
-
(1995)
Ann Neurol
, vol.38
, Issue.2
, pp. 267-269
-
-
Sivakumar, K.1
Cervenakova, L.2
Dalakas, M.C.3
-
34
-
-
39649123259
-
Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal
-
Needham M, Hooper A, James I, et al. Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal. Neuromuscul Dis. 2008;18(2):150–2.
-
(2008)
Neuromuscul Dis
, vol.18
, Issue.2
, pp. 150-152
-
-
Needham, M.1
Hooper, A.2
James, I.3
-
35
-
-
4844222812
-
ACT/AA polymorphism could duplicate the APOE*epsilon4-associated Alzheimer’s disease risk
-
Hernandez-Charro B, Moreno S, Valiente A, Manubens JM, Villar MD, Ramos-Arroyo MA. ACT/AA polymorphism could duplicate the APOE*epsilon4-associated Alzheimer’s disease risk. Med Clin. 2004;123(7):251–4.
-
(2004)
Med Clin
, vol.123
, Issue.7
, pp. 251-254
-
-
Hernandez-Charro, B.1
Moreno, S.2
Valiente, A.3
Manubens, J.M.4
Villar, M.D.5
Ramos-Arroyo, M.A.6
-
36
-
-
0027433773
-
Prion protein is abnormally accumulated in inclusion-body myositis
-
COI: 1:CAS:528:DyaK2cXhvVyrsL8%3D, PID: 8280854
-
Askanas V, Bilak M, Engel WK, Alvarez RB, Tome F, Leclerc A. Prion protein is abnormally accumulated in inclusion-body myositis. Neuroreport. 1993;5(1):25–8.
-
(1993)
Neuroreport
, vol.5
, Issue.1
, pp. 25-28
-
-
Askanas, V.1
Bilak, M.2
Engel, W.K.3
Alvarez, R.B.4
Tome, F.5
Leclerc, A.6
-
37
-
-
0033528207
-
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis
-
COI: 1:CAS:528:DyaK1MXht12qsL8%3D, PID: 9989722
-
Lampe J, Kitzler H, Walter MC, Lochmuller H, Reichmann H. Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis. Lancet. 1999;353(9151):465–6.
-
(1999)
Lancet
, vol.353
, Issue.9151
, pp. 465-466
-
-
Lampe, J.1
Kitzler, H.2
Walter, M.C.3
Lochmuller, H.4
Reichmann, H.5
-
38
-
-
0034711180
-
Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity
-
COI: 1:STN:280:DC%2BD3crhtlSisg%3D%3D, PID: 11071511
-
Orth M, Tabrizi SJ, Schapira AH. Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity. Neurology. 2000;55(8):1235.
-
(2000)
Neurology
, vol.55
, Issue.8
, pp. 1235
-
-
Orth, M.1
Tabrizi, S.J.2
Schapira, A.H.3
-
39
-
-
65349175153
-
TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies
-
COI: 1:CAS:528:DC%2BD1MXitlGgtb4%3D, PID: 19225410
-
Olive M, Janue A, Moreno D, Gamez J, Torrejon-Escribano B, Ferrer I. TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies. J Neuropathol Exp Neurol. 2009;68(3):262–73.
-
(2009)
J Neuropathol Exp Neurol
, vol.68
, Issue.3
, pp. 262-273
-
-
Olive, M.1
Janue, A.2
Moreno, D.3
Gamez, J.4
Torrejon-Escribano, B.5
Ferrer, I.6
-
40
-
-
67650264666
-
Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis
-
COI: 1:CAS:528:DC%2BD1MXptVaqtr4%3D, PID: 19533646
-
Salajegheh M, Pinkus JL, Taylor JP, et al. Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis. Muscle Nerve. 2009;40(1):19–31.
-
(2009)
Muscle Nerve
, vol.40
, Issue.1
, pp. 19-31
-
-
Salajegheh, M.1
Pinkus, J.L.2
Taylor, J.P.3
-
41
-
-
80855136462
-
Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient
-
PID: 20562395
-
Hernandez Lain A, Millecamps S, Dubourg O, et al. Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient. J Neurol Neurosurg Psychiatry. 2011;82(12):1414–6.
-
(2011)
J Neurol Neurosurg Psychiatry
, vol.82
, Issue.12
, pp. 1414-1416
-
-
Hernandez Lain, A.1
Millecamps, S.2
Dubourg, O.3
-
43
-
-
8944243541
-
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients
-
COI: 1:CAS:528:DyaK28Xkt1Omsbs%3D, PID: 8651651
-
Santorelli FM, Sciacco M, Tanji K, et al. Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients. Ann Neurol. 1996;39(6):789–95.
-
(1996)
Ann Neurol
, vol.39
, Issue.6
, pp. 789-795
-
-
Santorelli, F.M.1
Sciacco, M.2
Tanji, K.3
-
44
-
-
0030836286
-
Analysis of multiple mitochondrial DNA deletions in inclusion body myositis
-
COI: 1:CAS:528:DyaK2sXntlKjsbc%3D, PID: 9375854
-
Moslemi AR, Lindberg C, Oldfors A. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis. Hum Mutat. 1997;10(5):381–6.
-
(1997)
Hum Mutat
, vol.10
, Issue.5
, pp. 381-386
-
-
Moslemi, A.R.1
Lindberg, C.2
Oldfors, A.3
-
45
-
-
33644860811
-
Mitochondrial abnormalities in inclusion-body myositis
-
COI: 1:CAS:528:DC%2BD28Xht1KrtQ%3D%3D, PID: 16432145
-
Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C. Mitochondrial abnormalities in inclusion-body myositis. Neurology. 2006;66(2 Suppl 1):S49–55.
-
(2006)
Neurology
, vol.66
, Issue.2
, pp. S49-S55
-
-
Oldfors, A.1
Moslemi, A.R.2
Jonasson, L.3
Ohlsson, M.4
Kollberg, G.5
Lindberg, C.6
-
46
-
-
84867386549
-
TOMM40 association with Alzheimer disease: tales of APOE and linkage disequilibrium
-
PID: 22869030
-
Guerreiro RJ, Hardy J. TOMM40 association with Alzheimer disease: tales of APOE and linkage disequilibrium. Arch Neurol. 2012;69(10):1243–4.
-
(2012)
Arch Neurol
, vol.69
, Issue.10
, pp. 1243-1244
-
-
Guerreiro, R.J.1
Hardy, J.2
-
48
-
-
10744227832
-
Familial inclusion body myositis: a report on two Japanese sisters
-
Tateyama M, Saito N, Fujihara K, et al. Familial inclusion body myositis: a report on two Japanese sisters. Intern Med (Tokyo, Jpn). 2003;42(10):1035–8.
-
(2003)
Intern Med (Tokyo, Jpn)
, vol.42
, Issue.10
, pp. 1035-1038
-
-
Tateyama, M.1
Saito, N.2
Fujihara, K.3
-
49
-
-
0031002684
-
An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis
-
Sivakumar K, Semino-Mora C, Dalakas MC. An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Stud Three Fam Brain J Neurol. 1997;120(Pt 4):653–61.
-
(1997)
Stud Three Fam Brain J Neurol
, vol.120
, pp. 653-661
-
-
Sivakumar, K.1
Semino-Mora, C.2
Dalakas, M.C.3
-
50
-
-
16344371414
-
Familial inflammatory inclusion body myositis
-
COI: 1:STN:280:DC%2BD2M7jslGhtA%3D%3D, PID: 15769920
-
Ranque-Francois B, Maisonobe T, Dion E, et al. Familial inflammatory inclusion body myositis. Ann Rheum Dis. 2005;64(4):634–7.
-
(2005)
Ann Rheum Dis
, vol.64
, Issue.4
, pp. 634-637
-
-
Ranque-Francois, B.1
Maisonobe, T.2
Dion, E.3
-
51
-
-
84867330908
-
Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people
-
PID: 22349865
-
Cai H, Yabe I, Sato K, et al. Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people. J Neurol. 2012;259(9):1913–22.
-
(2012)
J Neurol
, vol.259
, Issue.9
, pp. 1913-1922
-
-
Cai, H.1
Yabe, I.2
Sato, K.3
-
52
-
-
0028787389
-
Inclusion body myositis and myopathies
-
COI: 1:STN:280:DyaK28%2FnsVWrsw%3D%3D, PID: 7486861
-
Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol. 1995;38(5):705–13.
-
(1995)
Ann Neurol
, vol.38
, Issue.5
, pp. 705-713
-
-
Griggs, R.C.1
Askanas, V.2
DiMauro, S.3
-
53
-
-
0029957253
-
Inclusion body myositis: clinical and pathological boundaries
-
COI: 1:STN:280:DyaK2s%2FisFertQ%3D%3D, PID: 8871577
-
Amato AA, Gronseth GS, Jackson CE, et al. Inclusion body myositis: clinical and pathological boundaries. Ann Neurol. 1996;40(4):581–6.
-
(1996)
Ann Neurol
, vol.40
, Issue.4
, pp. 581-586
-
-
Amato, A.A.1
Gronseth, G.S.2
Jackson, C.E.3
-
54
-
-
84885593282
-
Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features
-
PID: 23864699
-
Brady S, Squier W, Hilton-Jones D. Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features. J Neurol Neurosurg Psychiatry. 2013;84(11):1240–6.
-
(2013)
J Neurol Neurosurg Psychiatry
, vol.84
, Issue.11
, pp. 1240-1246
-
-
Brady, S.1
Squier, W.2
Hilton-Jones, D.3
-
55
-
-
0021176654
-
Monoclonal antibody analysis of mononuclear cells in myopathies. I: quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells
-
COI: 1:STN:280:DyaL2czgsFOgsQ%3D%3D, PID: 6383191
-
Arahata K, Engel AG. Monoclonal antibody analysis of mononuclear cells in myopathies. I: quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibers invaded by T cells. Ann Neurol. 1984;16(2):193–208.
-
(1984)
Ann Neurol
, vol.16
, Issue.2
, pp. 193-208
-
-
Arahata, K.1
Engel, A.G.2
-
56
-
-
84899544973
-
A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis
-
PID: 24776709, Study investigating the diagnostic utility of the histopathological features associated with IBM and proposing a diagnostic algorithm
-
Brady S, Squier W, Sewry C, Hanna M, Hilton-Jones D, Holton JL. A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis. BMJ Open. 2014;4(4):e004552. Study investigating the diagnostic utility of the histopathological features associated with IBM and proposing a diagnostic algorithm.
-
(2014)
BMJ Open
, vol.4
, Issue.4
, pp. e004552
-
-
Brady, S.1
Squier, W.2
Sewry, C.3
Hanna, M.4
Hilton-Jones, D.5
Holton, J.L.6
-
57
-
-
68149144251
-
How citation distortions create unfounded authority: analysis of a citation network
-
PID: 19622839
-
Greenberg SA. How citation distortions create unfounded authority: analysis of a citation network. BMJ. 2009;339:b2680.
-
(2009)
BMJ
, vol.339
, pp. b2680
-
-
Greenberg, S.A.1
-
58
-
-
85005769239
-
Comparative utility of LC3, p62 and TDP-43 immunohistochemistry in differentiation of inclusion body myositis from polymyositis and related inflammatory myopathies
-
PID: 24252466, Quantitative study of the diagnostic value of LC3, p62, and TDP-43 immunohistochemistry in IBM
-
Hiniker A, Daniels BH, Lee HS, Margeta M. Comparative utility of LC3, p62 and TDP-43 immunohistochemistry in differentiation of inclusion body myositis from polymyositis and related inflammatory myopathies. Acta Neuropathol Commun. 2013;1(1):29. Quantitative study of the diagnostic value of LC3, p62, and TDP-43 immunohistochemistry in IBM.
-
(2013)
Acta Neuropathol Commun
, vol.1
, Issue.1
, pp. 29
-
-
Hiniker, A.1
Daniels, B.H.2
Lee, H.S.3
Margeta, M.4
-
59
-
-
79956350423
-
Autoantibodies against a 43 KDa muscle protein in inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3MXmslCqs7Y%3D, PID: 21629782
-
Salajegheh M, Lam T, Greenberg SA. Autoantibodies against a 43 KDa muscle protein in inclusion body myositis. PLoS One. 2011;6(5):e20266.
-
(2011)
PLoS One
, vol.6
, Issue.5
, pp. e20266
-
-
Salajegheh, M.1
Lam, T.2
Greenberg, S.A.3
-
60
-
-
84915738111
-
Cytoplasmic 5′-nucleotidase autoantibodies in inclusion body myositis: isotypes and diagnostic utility
-
Greenberg SA. Cytoplasmic 5′-nucleotidase autoantibodies in inclusion body myositis: isotypes and diagnostic utility. Muscle Nerve 2014.
-
(2014)
Muscle Nerve
-
-
Greenberg, S.A.1
-
61
-
-
77957860016
-
Neuromuscular imaging in inherited muscle diseases
-
PID: 20422195
-
Wattjes MP, Kley RA, Fischer D. Neuromuscular imaging in inherited muscle diseases. Eur Radiol. 2010;20(10):2447–60.
-
(2010)
Eur Radiol
, vol.20
, Issue.10
, pp. 2447-2460
-
-
Wattjes, M.P.1
Kley, R.A.2
Fischer, D.3
-
62
-
-
12344263630
-
A comparison of inflammatory myopathies at whole-body turbo STIR MRI
-
COI: 1:STN:280:DC%2BD2M%2FjslSisg%3D%3D, PID: 15664582
-
Cantwell C, Ryan M, O’Connell M, et al. A comparison of inflammatory myopathies at whole-body turbo STIR MRI. Clin Radiol. 2005;60(2):261–7.
-
(2005)
Clin Radiol
, vol.60
, Issue.2
, pp. 261-267
-
-
Cantwell, C.1
Ryan, M.2
O’Connell, M.3
-
63
-
-
82155172633
-
Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis
-
PID: 21288962, Cross-sectional study of upper and lower extremity muscle MRI in a group of 32 patients with IBM
-
Cox FM, Reijnierse M, van Rijswijk CS, Wintzen AR, Verschuuren JJ, Badrising UA. Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis. Rheumatology. 2011;50(6):1153–61. Cross-sectional study of upper and lower extremity muscle MRI in a group of 32 patients with IBM.
-
(2011)
Rheumatology
, vol.50
, Issue.6
, pp. 1153-1161
-
-
Cox, F.M.1
Reijnierse, M.2
van Rijswijk, C.S.3
Wintzen, A.R.4
Verschuuren, J.J.5
Badrising, U.A.6
-
64
-
-
0034778644
-
Patterns of muscle involvement in inclusion body myositis: clinical and magnetic resonance imaging study
-
COI: 1:STN:280:DC%2BD3MnpsFygtg%3D%3D, PID: 11745956
-
Phillips BA, Cala LA, Thickbroom GW, Melsom A, Zilko PJ, Mastaglia FL. Patterns of muscle involvement in inclusion body myositis: clinical and magnetic resonance imaging study. Muscle Nerve. 2001;24(11):1526–34.
-
(2001)
Muscle Nerve
, vol.24
, Issue.11
, pp. 1526-1534
-
-
Phillips, B.A.1
Cala, L.A.2
Thickbroom, G.W.3
Melsom, A.4
Zilko, P.J.5
Mastaglia, F.L.6
-
65
-
-
0030989460
-
Magnetic resonance imaging of the forearm as a diagnostic aid in patients with sporadic inclusion body myositis
-
COI: 1:STN:280:DyaK2s3mtl2qtA%3D%3D, PID: 9109868
-
Sekul EA, Chow C, Dalakas MC. Magnetic resonance imaging of the forearm as a diagnostic aid in patients with sporadic inclusion body myositis. Neurology. 1997;48(4):863–6.
-
(1997)
Neurology
, vol.48
, Issue.4
, pp. 863-866
-
-
Sekul, E.A.1
Chow, C.2
Dalakas, M.C.3
-
66
-
-
0028219099
-
Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults
-
COI: 1:STN:280:DyaK2c3nsFGjtA%3D%3D, PID: 8006684
-
Reimers CD, Schedel H, Fleckenstein JL, et al. Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults. J Neurol. 1994;241(5):306–14.
-
(1994)
J Neurol
, vol.241
, Issue.5
, pp. 306-314
-
-
Reimers, C.D.1
Schedel, H.2
Fleckenstein, J.L.3
-
67
-
-
0025831477
-
Three-point Dixon technique for true water/fat decomposition with B0 inhomogeneity correction
-
COI: 1:STN:280:DyaK3M3mtVCjsQ%3D%3D
-
Glover GH, Schneider E. Three-point Dixon technique for true water/fat decomposition with B0 inhomogeneity correction. Magn Reson Medi Off J Soc Magn Reson Med Soc Magn Reson Med. 1991;18(2):371–83.
-
(1991)
Magn Reson Medi Off J Soc Magn Reson Med Soc Magn Reson Med
, vol.18
, Issue.2
, pp. 371-383
-
-
Glover, G.H.1
Schneider, E.2
-
68
-
-
62649111494
-
K+-dependent paradoxical membrane depolarization and Na+overload, major and reversible contributors to weakness by ion channel leaks
-
COI: 1:CAS:528:DC%2BD1MXjt1eisL4%3D, PID: 19225109
-
Jurkat-Rott K, Weber MA, Fauler M, et al. K+-dependent paradoxical membrane depolarization and Na+overload, major and reversible contributors to weakness by ion channel leaks. Proc Natl Acad Sci U S A. 2009;106(10):4036–41.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.10
, pp. 4036-4041
-
-
Jurkat-Rott, K.1
Weber, M.A.2
Fauler, M.3
-
69
-
-
84902360840
-
-
Reproducibility, and age, body-weight and gender dependency of candidate skeletal muscle MRI outcome measures in healthy volunteers, Eur Radiol:
-
Morrow JM, Sinclair CD, Fischmann A, et al. Reproducibility, and age, body-weight and gender dependency of candidate skeletal muscle MRI outcome measures in healthy volunteers. Eur Radiol. 2014.
-
(2014)
et al
-
-
Morrow, J.M.1
Sinclair, C.D.2
Fischmann, A.3
-
70
-
-
84878878617
-
MRI quantification of lower limb muscle fatty atrophy: a potential outcome measure in chronic neuromuscular diseases
-
Morrow J, Sinclair CDJ, Fischmann A, et al. MRI quantification of lower limb muscle fatty atrophy: a potential outcome measure in chronic neuromuscular diseases. J Neurol Neurosurg Psychiatry. 2012;83:e1.
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. e1
-
-
Morrow, J.1
Sinclair, C.D.J.2
Fischmann, A.3
-
71
-
-
84888431952
-
188th ENMC International Workshop: inclusion body myositis, 2-4 December 2011, Naarden, The Netherlands
-
Report of an international workshop that resulted in the publication of revised research diagnostic criteria for IBM
-
Rose MR, Group EIW. 188th ENMC International Workshop: inclusion body myositis, 2-4 December 2011, Naarden, The Netherlands. Neuromuscul Dis. 2013;23(12):1044–55. Report of an international workshop that resulted in the publication of revised research diagnostic criteria for IBM.
-
(2013)
Neuromuscul Dis
, vol.23
, Issue.12
, pp. 1044-1055
-
-
Rose, M.R.1
Group EIW, E.I.W.2
-
72
-
-
75149122299
-
Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June 2008
-
COI: 1:STN:280:DC%2BC3c%2FpsVequg%3D%3D
-
Hilton-Jones D, Miller A, Parton M, Holton J, Sewry C, Hanna MG. Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June 2008. Neuromuscul Dis. 2010;20(2):142–7.
-
(2010)
Neuromuscul Dis
, vol.20
, Issue.2
, pp. 142-147
-
-
Hilton-Jones, D.1
Miller, A.2
Parton, M.3
Holton, J.4
Sewry, C.5
Hanna, M.G.6
-
73
-
-
77953122090
-
International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009
-
Benveniste O, Hilton-Jones D. International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009. Neuromuscul Dis. 2010;20(6):414–21.
-
(2010)
Neuromuscul Dis
, vol.20
, Issue.6
, pp. 414-421
-
-
Benveniste, O.1
Hilton-Jones, D.2
-
74
-
-
84919818955
-
-
Neurology: Analysis of the diagnostic performance of published IBM diagnostic categories and individual IBM features
-
Lloyd TE, Mammen AL, Amato AA, Weiss MD, Needham M, Greenberg SA. Evaluation and construction of diagnostic criteria for inclusion body myositis. Neurology 2014. Analysis of the diagnostic performance of published IBM diagnostic categories and individual IBM features.
-
(2014)
Evaluation and construction of diagnostic criteria for inclusion body myositis
-
-
Lloyd, T.E.1
Mammen, A.L.2
Amato, A.A.3
Weiss, M.D.4
Needham, M.5
Greenberg, S.A.6
-
75
-
-
38749111772
-
Sporadic inclusion body myositis: a continuing puzzle
-
COI: 1:STN:280:DC%2BD1c%2FosVCmuw%3D%3D
-
Needham M, Mastaglia FL. Sporadic inclusion body myositis: a continuing puzzle. Neuromuscul Dis. 2008;18(1):6–16.
-
(2008)
Neuromuscul Dis
, vol.18
, Issue.1
, pp. 6-16
-
-
Needham, M.1
Mastaglia, F.L.2
-
76
-
-
77953476411
-
Theories of the pathogenesis of inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3cXht1CjsbrL, PID: 20425523
-
Greenberg SA. Theories of the pathogenesis of inclusion body myositis. Curr Rheumatol Rep. 2010;12(3):221–8.
-
(2010)
Curr Rheumatol Rep
, vol.12
, Issue.3
, pp. 221-228
-
-
Greenberg, S.A.1
-
77
-
-
33746530058
-
Sporadic inclusion body myositis–diagnosis, pathogenesis and therapeutic strategies. Nature clinical practice
-
COI: 1:CAS:528:DC%2BD28Xot1yht7c%3D, PID: 16932602
-
Dalakas MC. Sporadic inclusion body myositis–diagnosis, pathogenesis and therapeutic strategies. Nature clinical practice. Neurology. 2006;2(8):437–47.
-
(2006)
Neurology
, vol.2
, Issue.8
, pp. 437-447
-
-
Dalakas, M.C.1
-
78
-
-
34948816592
-
Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis
-
PID: 17917534
-
Askanas V, Engel WK. Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis. Curr Opin Rheumatol. 2007;19(6):550–9.
-
(2007)
Curr Opin Rheumatol
, vol.19
, Issue.6
, pp. 550-559
-
-
Askanas, V.1
Engel, W.K.2
-
79
-
-
84898657573
-
Inhibition of myogenic microRNAs 1, 133, and 206 by inflammatory cytokines links inflammation and muscle degeneration in adult inflammatory myopathies
-
COI: 1:CAS:528:DC%2BC2cXhtl2qur7I, PID: 24757153
-
Georgantas RW, Streicher K, Greenberg SA, et al. Inhibition of myogenic microRNAs 1, 133, and 206 by inflammatory cytokines links inflammation and muscle degeneration in adult inflammatory myopathies. Arthritis Rheumatol. 2014;66(4):1022–33.
-
(2014)
Arthritis Rheumatol
, vol.66
, Issue.4
, pp. 1022-1033
-
-
Georgantas, R.W.1
Streicher, K.2
Greenberg, S.A.3
-
80
-
-
84903737968
-
Mitochondrial and inflammatory changes in sporadic Inclusion Body Myositis
-
Rygiel KA, Miller J, Grady JP, Rocha MC, Taylor RW, Turnbull DM. Mitochondrial and inflammatory changes in sporadic Inclusion Body Myositis. Neuropathol Appl Neurobiol. 2014.
-
(2014)
Neuropathol Appl Neurobiol
-
-
Rygiel, K.A.1
Miller, J.2
Grady, J.P.3
Rocha, M.C.4
Taylor, R.W.5
Turnbull, D.M.6
-
81
-
-
58749094423
-
Inflammatory myopathies with mitochondrial pathology and protein aggregates
-
PID: 19101700
-
Temiz P, Weihl CC, Pestronk A. Inflammatory myopathies with mitochondrial pathology and protein aggregates. J Neurol Sci. 2009;278(1–2):25–9.
-
(2009)
J Neurol Sci
, vol.278
, Issue.1-2
, pp. 25-29
-
-
Temiz, P.1
Weihl, C.C.2
Pestronk, A.3
-
82
-
-
84901988674
-
Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis
-
Pinkus JL, Amato AA, Taylor JP, Greenberg SA. Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis. Neuromuscul Dis. 2014;24(7):611–6.
-
(2014)
Neuromuscul Dis
, vol.24
, Issue.7
, pp. 611-616
-
-
Pinkus, J.L.1
Amato, A.A.2
Taylor, J.P.3
Greenberg, S.A.4
-
83
-
-
84903372127
-
Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy
-
COI: 1:CAS:528:DC%2BC2cXht1Gqsro%3D, PID: 24462217
-
Cortese A, Plagnol V, Brady S, et al. Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy. Neurobiol Aging. 2014;35(6):1491–8.
-
(2014)
Neurobiol Aging
, vol.35
, Issue.6
, pp. 1491-1498
-
-
Cortese, A.1
Plagnol, V.2
Brady, S.3
-
84
-
-
33749419659
-
Nuclear membrane proteins are present within rimmed vacuoles in inclusion-body myositis
-
COI: 1:CAS:528:DC%2BD28XhtFChsbjN, PID: 16823856
-
Greenberg SA, Pinkus JL, Amato AA. Nuclear membrane proteins are present within rimmed vacuoles in inclusion-body myositis. Muscle Nerve. 2006;34(4):406–16.
-
(2006)
Muscle Nerve
, vol.34
, Issue.4
, pp. 406-416
-
-
Greenberg, S.A.1
Pinkus, J.L.2
Amato, A.A.3
-
85
-
-
38649134132
-
Histone H1 is released from myonuclei and present in rimmed vacuoles with DNA in inclusion body myositis
-
Nakano S, Shinde A, Fujita K, Ito H, Kusaka H. Histone H1 is released from myonuclei and present in rimmed vacuoles with DNA in inclusion body myositis. Neuromuscul Dis. 2008;18(1):27–33.
-
(2008)
Neuromuscul Dis
, vol.18
, Issue.1
, pp. 27-33
-
-
Nakano, S.1
Shinde, A.2
Fujita, K.3
Ito, H.4
Kusaka, H.5
-
86
-
-
0028230941
-
Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositis
-
COI: 1:CAS:528:DyaK2cXltlWmur0%3D, PID: 8178939
-
Nalbantoglu J, Karpati G, Carpenter S. Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositis. Am J Pathol. 1994;144(5):874–82.
-
(1994)
Am J Pathol
, vol.144
, Issue.5
, pp. 874-882
-
-
Nalbantoglu, J.1
Karpati, G.2
Carpenter, S.3
-
87
-
-
68349097450
-
p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis
-
COI: 1:CAS:528:DC%2BD1MXptVGjt7g%3D, PID: 19557423
-
Nogalska A, Terracciano C, D’Agostino C, King Engel W, Askanas V. p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis. Acta Neuropathol. 2009;118(3):407–13.
-
(2009)
Acta Neuropathol
, vol.118
, Issue.3
, pp. 407-413
-
-
Nogalska, A.1
Terracciano, C.2
D’Agostino, C.3
King Engel, W.4
Askanas, V.5
-
88
-
-
79951804430
-
In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments
-
PID: 20626631
-
D’Agostino C, Nogalska A, Engel WK, Askanas V. In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments. Neuropathol Appl Neurobiol. 2011;37(3):315–20.
-
(2011)
Neuropathol Appl Neurobiol
, vol.37
, Issue.3
, pp. 315-320
-
-
D’Agostino, C.1
Nogalska, A.2
Engel, W.K.3
Askanas, V.4
-
89
-
-
77953180920
-
p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system
-
COI: 1:CAS:528:DC%2BC3cXot1ehsb0%3D, PID: 20083896
-
Ju JS, Weihl CC. p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system. Autophagy. 2010;6(2):283–5.
-
(2010)
Autophagy
, vol.6
, Issue.2
, pp. 283-285
-
-
Ju, J.S.1
Weihl, C.C.2
-
90
-
-
66949145779
-
Inclusion body myositis: a degenerative muscle disease associated with intra-muscle fiber multi-protein aggregates, proteasome inhibition, endoplasmic reticulum stress and decreased lysosomal degradation
-
COI: 1:CAS:528:DC%2BD1MXos1Ojt7g%3D
-
Askanas V, Engel WK, Nogalska A. Inclusion body myositis: a degenerative muscle disease associated with intra-muscle fiber multi-protein aggregates, proteasome inhibition, endoplasmic reticulum stress and decreased lysosomal degradation. Brain Pathol (Zurich, Switzerland). 2009;19(3):493–506.
-
(2009)
Brain Pathol (Zurich, Switzerland)
, vol.19
, Issue.3
, pp. 493-506
-
-
Askanas, V.1
Engel, W.K.2
Nogalska, A.3
-
91
-
-
77956393778
-
Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers
-
COI: 1:CAS:528:DC%2BC3cXhtV2gsbvM, PID: 20664349
-
Weihl CC, Pestronk A. Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers. Curr Opin Neurol. 2010;23(5):482–8.
-
(2010)
Curr Opin Neurol
, vol.23
, Issue.5
, pp. 482-488
-
-
Weihl, C.C.1
Pestronk, A.2
-
92
-
-
2442651500
-
Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis
-
COI: 1:CAS:528:DC%2BD2cXlt1emu7c%3D, PID: 15198127
-
Ferrer I, Martin B, Castano JG, Lucas JJ, Moreno D, Olive M. Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis. J Neuropathol Exp Neurol. 2004;63(5):484–98.
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, Issue.5
, pp. 484-498
-
-
Ferrer, I.1
Martin, B.2
Castano, J.G.3
Lucas, J.J.4
Moreno, D.5
Olive, M.6
-
93
-
-
4644328932
-
Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers
-
COI: 1:CAS:528:DC%2BD2cXntlOrsrY%3D, PID: 15452314
-
Fratta P, Engel WK, Van Leeuwen FW, Hol EM, Vattemi G, Askanas V. Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers. Neurology. 2004;63(6):1114–7.
-
(2004)
Neurology
, vol.63
, Issue.6
, pp. 1114-1117
-
-
Fratta, P.1
Engel, W.K.2
Van Leeuwen, F.W.3
Hol, E.M.4
Vattemi, G.5
Askanas, V.6
-
94
-
-
84886770674
-
Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres
-
COI: 1:CAS:528:DC%2BC3sXhslWms7rP, PID: 23452232
-
Cacciottolo M, Nogalska A, D’Agostino C, Engel WK, Askanas V. Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres. Neuropathol Appl Neurobiol. 2013;39(7):750–61.
-
(2013)
Neuropathol Appl Neurobiol
, vol.39
, Issue.7
, pp. 750-761
-
-
Cacciottolo, M.1
Nogalska, A.2
D’Agostino, C.3
Engel, W.K.4
Askanas, V.5
-
95
-
-
84886790407
-
Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis
-
COI: 1:CAS:528:DC%2BC3sXhslWms7rI, PID: 23452291
-
Girolamo F, Lia A, Amati A, et al. Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis. Neuropathol Appl Neurobiol. 2013;39(7):736–49.
-
(2013)
Neuropathol Appl Neurobiol
, vol.39
, Issue.7
, pp. 736-749
-
-
Girolamo, F.1
Lia, A.2
Amati, A.3
-
96
-
-
82355175806
-
Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis
-
PID: 21935636
-
D’Agostino C, Nogalska A, Cacciottolo M, Engel WK, Askanas V. Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis. Acta Neuropathol. 2011;122(5):627–36.
-
(2011)
Acta Neuropathol
, vol.122
, Issue.5
, pp. 627-636
-
-
D’Agostino, C.1
Nogalska, A.2
Cacciottolo, M.3
Engel, W.K.4
Askanas, V.5
-
97
-
-
1542784578
-
Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle
-
COI: 1:CAS:528:DC%2BD2cXlsVChsA%3D%3D, PID: 14695312
-
Vattemi G, Engel WK, McFerrin J, Askanas V. Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle. Am J Pathol. 2004;164(1):1–7.
-
(2004)
Am J Pathol
, vol.164
, Issue.1
, pp. 1-7
-
-
Vattemi, G.1
Engel, W.K.2
McFerrin, J.3
Askanas, V.4
-
98
-
-
31144470450
-
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
-
COI: 1:CAS:528:DC%2BD28XktF2huw%3D%3D, PID: 16321991
-
Weihl CC, Dalal S, Pestronk A, Hanson PI. Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Hum Mol Genet. 2006;15(2):189–99.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.2
, pp. 189-199
-
-
Weihl, C.C.1
Dalal, S.2
Pestronk, A.3
Hanson, P.I.4
-
99
-
-
0032576605
-
Aggresomes: a cellular response to misfolded proteins
-
COI: 1:CAS:528:DyaK1MXisFCrtA%3D%3D, PID: 9864362
-
Johnston JA, Ward CL, Kopito RR. Aggresomes: a cellular response to misfolded proteins. J Cell Biol. 1998;143(7):1883–98.
-
(1998)
J Cell Biol
, vol.143
, Issue.7
, pp. 1883-1898
-
-
Johnston, J.A.1
Ward, C.L.2
Kopito, R.R.3
-
101
-
-
41549084155
-
Transforming growth factor-beta and myostatin signaling in skeletal muscle
-
COI: 1:CAS:528:DC%2BD1cXkt1Ohtrw%3D, PID: 18032576
-
Kollias HD, McDermott JC. Transforming growth factor-beta and myostatin signaling in skeletal muscle. J Appl Physiol. 2008;104(3):579–87.
-
(2008)
J Appl Physiol
, vol.104
, Issue.3
, pp. 579-587
-
-
Kollias, H.D.1
McDermott, J.C.2
-
102
-
-
0031010050
-
Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member
-
COI: 1:CAS:528:DyaK2sXivFygur0%3D, PID: 9139826
-
McPherron AC, Lawler AM, Lee SJ. Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member. Nature. 1997;387(6628):83–90.
-
(1997)
Nature
, vol.387
, Issue.6628
, pp. 83-90
-
-
McPherron, A.C.1
Lawler, A.M.2
Lee, S.J.3
-
103
-
-
0030818314
-
Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle
-
COI: 1:CAS:528:DyaK2sXmtVSlu7w%3D, PID: 9314496
-
Kambadur R, Sharma M, Smith TP, Bass JJ. Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle. Genome Res. 1997;7(9):910–6.
-
(1997)
Genome Res
, vol.7
, Issue.9
, pp. 910-916
-
-
Kambadur, R.1
Sharma, M.2
Smith, T.P.3
Bass, J.J.4
-
104
-
-
0030840359
-
Double muscling in cattle due to mutations in the myostatin gene
-
COI: 1:CAS:528:DyaK2sXns1ylsbk%3D, PID: 9356471
-
McPherron AC, Lee SJ. Double muscling in cattle due to mutations in the myostatin gene. Proc Natl Acad Sci U S A. 1997;94(23):12457–61.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, Issue.23
, pp. 12457-12461
-
-
McPherron, A.C.1
Lee, S.J.2
-
105
-
-
34249733201
-
A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs
-
PID: 17530926
-
Mosher DS, Quignon P, Bustamante CD, et al. A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs. PLoS Genet. 2007;3(5):e79.
-
(2007)
PLoS Genet
, vol.3
, Issue.5
, pp. e79
-
-
Mosher, D.S.1
Quignon, P.2
Bustamante, C.D.3
-
106
-
-
2942735123
-
Myostatin mutation associated with gross muscle hypertrophy in a child
-
COI: 1:CAS:528:DC%2BD2cXltFGns7c%3D, PID: 15215484
-
Schuelke M, Wagner KR, Stolz LE, et al. Myostatin mutation associated with gross muscle hypertrophy in a child. N Engl J Med. 2004;350(26):2682–8.
-
(2004)
N Engl J Med
, vol.350
, Issue.26
, pp. 2682-2688
-
-
Schuelke, M.1
Wagner, K.R.2
Stolz, L.E.3
-
107
-
-
33745805890
-
Myostatin: biology and clinical relevance
-
COI: 1:CAS:528:DC%2BD28XlvFCnsL8%3D, PID: 16842126
-
Carnac G, Ricaud S, Vernus B, Bonnieu A. Myostatin: biology and clinical relevance. Mini Rev Med Chem. 2006;6(7):765–70.
-
(2006)
Mini Rev Med Chem
, vol.6
, Issue.7
, pp. 765-770
-
-
Carnac, G.1
Ricaud, S.2
Vernus, B.3
Bonnieu, A.4
-
108
-
-
44849140764
-
A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy
-
COI: 1:CAS:528:DC%2BD1cXntFyrtrs%3D, PID: 18335515
-
Wagner KR, Fleckenstein JL, Amato AA, et al. A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy. Ann Neurol. 2008;63(5):561–71.
-
(2008)
Ann Neurol
, vol.63
, Issue.5
, pp. 561-571
-
-
Wagner, K.R.1
Fleckenstein, J.L.2
Amato, A.A.3
-
109
-
-
84919818954
-
-
. Efficacy, safety and tolerability of BYM338 in patients with sporadic inclusion body myositis. Accessed 20 Jun 2014
-
http://www.clinicaltrials.gov/ct2/show/NCT01423110. Efficacy, safety and tolerability of BYM338 in patients with sporadic inclusion body myositis. Accessed 20 Jun 2014.
-
-
-
-
110
-
-
39749114099
-
Myostatin blockade improves function but not histopathology in a murine model of limb-girdle muscular dystrophy 2C
-
COI: 1:CAS:528:DC%2BD1cXjs1eqtLY%3D, PID: 18041051
-
Bogdanovich S, McNally EM, Khurana TS. Myostatin blockade improves function but not histopathology in a murine model of limb-girdle muscular dystrophy 2C. Muscle Nerve. 2008;37(3):308–16.
-
(2008)
Muscle Nerve
, vol.37
, Issue.3
, pp. 308-316
-
-
Bogdanovich, S.1
McNally, E.M.2
Khurana, T.S.3
-
111
-
-
34247166670
-
AAV-mediated delivery of a mutated myostatin propeptide ameliorates calpain 3 but not alpha-sarcoglycan deficiency
-
COI: 1:CAS:528:DC%2BD2sXkt1Kjsbg%3D, PID: 17330087
-
Bartoli M, Poupiot J, Vulin A, et al. AAV-mediated delivery of a mutated myostatin propeptide ameliorates calpain 3 but not alpha-sarcoglycan deficiency. Gene Ther. 2007;14(9):733–40.
-
(2007)
Gene Ther
, vol.14
, Issue.9
, pp. 733-740
-
-
Bartoli, M.1
Poupiot, J.2
Vulin, A.3
-
112
-
-
77956029835
-
Administration of a soluble activin type IIB receptor promotes skeletal muscle growth independent of fiber type
-
COI: 1:CAS:528:DC%2BC3cXht1SqtbnE, PID: 20466801
-
Cadena SM, Tomkinson KN, Monnell TE, et al. Administration of a soluble activin type IIB receptor promotes skeletal muscle growth independent of fiber type. J Appl Physiol. 2010;109(3):635–42.
-
(2010)
J Appl Physiol
, vol.109
, Issue.3
, pp. 635-642
-
-
Cadena, S.M.1
Tomkinson, K.N.2
Monnell, T.E.3
-
113
-
-
62849108016
-
Inhibition of myostatin with emphasis on follistatin as a therapy for muscle disease
-
COI: 1:CAS:528:DC%2BD1MXjvVajsbs%3D, PID: 19208403
-
Rodino-Klapac LR, Haidet AM, Kota J, Handy C, Kaspar BK, Mendell JR. Inhibition of myostatin with emphasis on follistatin as a therapy for muscle disease. Muscle Nerve. 2009;39(3):283–96.
-
(2009)
Muscle Nerve
, vol.39
, Issue.3
, pp. 283-296
-
-
Rodino-Klapac, L.R.1
Haidet, A.M.2
Kota, J.3
Handy, C.4
Kaspar, B.K.5
Mendell, J.R.6
-
114
-
-
41949090708
-
Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors
-
COI: 1:CAS:528:DC%2BD1cXktF2ktbw%3D, PID: 18334646
-
Haidet AM, Rizo L, Handy C, et al. Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors. Proc Natl Acad Sci U S A. 2008;105(11):4318–22.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, Issue.11
, pp. 4318-4322
-
-
Haidet, A.M.1
Rizo, L.2
Handy, C.3
-
115
-
-
2342627231
-
Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin
-
Lezzi S, Di Padova M, Serra C, et al. Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin. Dev Cell. 2004;6(5):673–84.
-
(2004)
Dev Cell
, vol.6
, Issue.5
, pp. 673-684
-
-
Lezzi, S.1
Di Padova, M.2
Serra, C.3
-
116
-
-
33749507982
-
Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors
-
COI: 1:CAS:528:DC%2BD28XhtVChsrjN, PID: 16980968
-
Minetti GC, Colussi C, Adami R, et al. Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors. Nat Med. 2006;12(10):1147–50.
-
(2006)
Nat Med
, vol.12
, Issue.10
, pp. 1147-1150
-
-
Minetti, G.C.1
Colussi, C.2
Adami, R.3
-
117
-
-
24344458115
-
Myostatin is increased and complexes with amyloid-beta within sporadic inclusion-body myositis muscle fibers
-
COI: 1:CAS:528:DC%2BD2MXos1CqurY%3D, PID: 15983828
-
Wojcik S, Engel WK, McFerrin J, Askanas V. Myostatin is increased and complexes with amyloid-beta within sporadic inclusion-body myositis muscle fibers. Acta Neuropathol. 2005;110(2):173–7.
-
(2005)
Acta Neuropathol
, vol.110
, Issue.2
, pp. 173-177
-
-
Wojcik, S.1
Engel, W.K.2
McFerrin, J.3
Askanas, V.4
-
118
-
-
33749254273
-
Myostatin induces cachexia by activating the ubiquitin proteolytic system through an NF-kappaB-independent, FoxO1-dependent mechanism
-
COI: 1:CAS:528:DC%2BD28XhtVClu7fL, PID: 16883577
-
McFarlane C, Plummer E, Thomas M, et al. Myostatin induces cachexia by activating the ubiquitin proteolytic system through an NF-kappaB-independent, FoxO1-dependent mechanism. J Cell Physiol. 2006;209(2):501–14.
-
(2006)
J Cell Physiol
, vol.209
, Issue.2
, pp. 501-514
-
-
McFarlane, C.1
Plummer, E.2
Thomas, M.3
-
119
-
-
14644400387
-
TNF-alpha acts via p38 MAPK to stimulate expression of the ubiquitin ligase atrogin1/MAFbx in skeletal muscle
-
COI: 1:CAS:528:DC%2BD2MXit1ygsbY%3D
-
Li YP, Chen Y, John J, et al. TNF-alpha acts via p38 MAPK to stimulate expression of the ubiquitin ligase atrogin1/MAFbx in skeletal muscle. FASEB J Off Publ Fed Am Soc Exp Biol. 2005;19(3):362–70.
-
(2005)
FASEB J Off Publ Fed Am Soc Exp Biol
, vol.19
, Issue.3
, pp. 362-370
-
-
Li, Y.P.1
Chen, Y.2
John, J.3
-
120
-
-
84862824616
-
Foxo/atrogin induction in human and experimental myositis
-
COI: 1:CAS:528:DC%2BC38Xltlansrw%3D, PID: 22590725
-
Lee HK, Rocnik E, Fu Q, et al. Foxo/atrogin induction in human and experimental myositis. Neurobiol Dis. 2012;46(2):463–75.
-
(2012)
Neurobiol Dis
, vol.46
, Issue.2
, pp. 463-475
-
-
Lee, H.K.1
Rocnik, E.2
Fu, Q.3
-
121
-
-
73249151002
-
Expression of the dermatomyositis autoantigen Mi-2 in regenerating muscle
-
COI: 1:CAS:528:DC%2BC3cXhtFKhtb%2FE, PID: 19950298
-
Mammen AL, Casciola-Rosen LA, Hall JC, Christopher-Stine L, Corse AM, Rosen A. Expression of the dermatomyositis autoantigen Mi-2 in regenerating muscle. Arthritis Rheum. 2009;60(12):3784–93.
-
(2009)
Arthritis Rheum
, vol.60
, Issue.12
, pp. 3784-3793
-
-
Mammen, A.L.1
Casciola-Rosen, L.A.2
Hall, J.C.3
Christopher-Stine, L.4
Corse, A.M.5
Rosen, A.6
-
122
-
-
84866329572
-
Pathogenesis and therapy of inclusion body myositis
-
PID: 22941263
-
Greenberg SA. Pathogenesis and therapy of inclusion body myositis. Curr Opin Neurol. 2012;25(5):630–9.
-
(2012)
Curr Opin Neurol
, vol.25
, Issue.5
, pp. 630-639
-
-
Greenberg, S.A.1
-
123
-
-
84886717183
-
Safety and tolerability of arimoclomol in patients with sporadic inclusion body myositis: a randomised, double-blind, placebo-controlled, phase IIa proof-of-concept trial
-
Machado P, Miller A, Herbelin L, et al. Safety and tolerability of arimoclomol in patients with sporadic inclusion body myositis: a randomised, double-blind, placebo-controlled, phase IIa proof-of-concept trial. Ann Rheum Dis. 2013;72 Suppl 3:164.
-
(2013)
Ann Rheum Dis
, vol.72
, pp. 164
-
-
Machado, P.1
Miller, A.2
Herbelin, L.3
-
124
-
-
84919818953
-
-
. Arimoclomol in Sporadic Inclusion Body Myositis. Accessed 20 Jun 2014
-
http://www.clinicaltrials.gov/ct2/show/NCT00769860. Arimoclomol in Sporadic Inclusion Body Myositis. Accessed 20 Jun 2014.
-
-
-
-
125
-
-
84919818952
-
-
. Follistatin gene transfer to patients with becker muscular dystrophy and sporadic inclusion body myositis. Accessed 20 Jun 2014
-
http://www.clinicaltrials.gov/ct2/show/NCT01519349. Follistatin gene transfer to patients with becker muscular dystrophy and sporadic inclusion body myositis. Accessed 20 Jun 2014.
-
-
-
-
126
-
-
84907609783
-
Treatment of sporadic inclusion body myositis with an anti-activin receptor IIB antibody
-
Amato AA, Sivakumar K, Goyal N, et al. Treatment of sporadic inclusion body myositis with an anti-activin receptor IIB antibody. Ann Neurol. 2013;74:S93–4.
-
(2013)
Ann Neurol
, vol.74
, pp. S93-S94
-
-
Amato, A.A.1
Sivakumar, K.2
Goyal, N.3
-
127
-
-
84919818951
-
-
. Efficacy and safety of Bimagrumab/BYM338 at 52 weeks on physical function, muscle strength, mobility in sIBM patients (RESILIENT). Accessed 20 Jun 2014
-
http://www.clinicaltrials.gov/ct2/show/NCT01925209. Efficacy and safety of Bimagrumab/BYM338 at 52 weeks on physical function, muscle strength, mobility in sIBM patients (RESILIENT). Accessed 20 Jun 2014.
-
-
-
-
128
-
-
84864031189
-
The pandemic of physical inactivity: global action for public health
-
PID: 22818941
-
Kohl HW, Craig CL, Lambert EV, et al. The pandemic of physical inactivity: global action for public health. Lancet. 2012;380(9838):294–305.
-
(2012)
Lancet
, vol.380
, Issue.9838
, pp. 294-305
-
-
Kohl, H.W.1
Craig, C.L.2
Lambert, E.V.3
-
129
-
-
84901610031
-
New insights into the benefits of exercise for muscle health in patients with idiopathic inflammatory myositis
-
PID: 24879535, Recent review article about the beneficial effects of exercise in polymyositis, dermatomyositis, and IBM
-
Alemo Munters L, Alexanderson H, Crofford LJ, Lundberg IE. New insights into the benefits of exercise for muscle health in patients with idiopathic inflammatory myositis. Curr Rheumatol Rep. 2014;16(7):429. Recent review article about the beneficial effects of exercise in polymyositis, dermatomyositis, and IBM.
-
(2014)
Curr Rheumatol Rep
, vol.16
, Issue.7
, pp. 429
-
-
Alemo Munters, L.1
Alexanderson, H.2
Crofford, L.J.3
Lundberg, I.E.4
-
130
-
-
0036838252
-
-
Fowler WM, Jr. Consensus conference summary: role of physical activity and exercise training in neuromuscular diseases. J Phys Med. 2002;81(11)
-
Fowler WM, Jr. Consensus conference summary: role of physical activity and exercise training in neuromuscular diseases. J Phys Med. 2002;81(11).
-
-
-
-
131
-
-
0030855924
-
Safety and efficacy of strength training in patients with sporadic inclusion body myositis
-
COI: 1:STN:280:DyaK2svmsVamuw%3D%3D, PID: 9324080
-
Spector SA, Lemmer JT, Koffman BM, et al. Safety and efficacy of strength training in patients with sporadic inclusion body myositis. Muscle Nerve. 1997;20(10):1242–8.
-
(1997)
Muscle Nerve
, vol.20
, Issue.10
, pp. 1242-1248
-
-
Spector, S.A.1
Lemmer, J.T.2
Koffman, B.M.3
-
132
-
-
12244300976
-
Sporadic inclusion body myositis: pilot study on the effects of a home exercise program on muscle function, histopathology and inflammatory reaction
-
PID: 12610846
-
Arnardottir S, Alexanderson H, Lundberg IE, Borg K. Sporadic inclusion body myositis: pilot study on the effects of a home exercise program on muscle function, histopathology and inflammatory reaction. J Rehabil Med. 2003;35(1):31–5.
-
(2003)
J Rehabil Med
, vol.35
, Issue.1
, pp. 31-35
-
-
Arnardottir, S.1
Alexanderson, H.2
Lundberg, I.E.3
Borg, K.4
-
133
-
-
34447338318
-
-
Johnson LG, Edwards DJ, Walters S, Thickbroom GW, Mastaglia FL. The effectiveness of an individualized, home-based functional exercise program for patients with sporadic inclusion body myositis. J Clin Neuromuscul Dis. 2007;8(4)
-
Johnson LG, Edwards DJ, Walters S, Thickbroom GW, Mastaglia FL. The effectiveness of an individualized, home-based functional exercise program for patients with sporadic inclusion body myositis. J Clin Neuromuscul Dis. 2007;8(4).
-
-
-
-
134
-
-
84855834307
-
Knee extensor strength exhibits potential to predict function in sporadic inclusion-body myositis
-
PID: 22246869
-
Lowes LP, Alfano L, Viollet L, et al. Knee extensor strength exhibits potential to predict function in sporadic inclusion-body myositis. Muscle Nerve. 2012;45(2):163–8.
-
(2012)
Muscle Nerve
, vol.45
, Issue.2
, pp. 163-168
-
-
Lowes, L.P.1
Alfano, L.2
Viollet, L.3
-
135
-
-
80355135347
-
-
Gualano B, Ugrinowitsch C, Neves Jr M, et al. Vascular occlusion training for inclusion body myositis: a novel therapeutic approach. J Vis Exp. 2010(40)
-
Gualano B, Ugrinowitsch C, Neves Jr M, et al. Vascular occlusion training for inclusion body myositis: a novel therapeutic approach. J Vis Exp. 2010(40).
-
-
-
-
136
-
-
0031862877
-
Energy expenditure, physical activity, and body composition of ambulatory adults with hereditary neuromuscular disease
-
COI: 1:CAS:528:DyaK1cXjsFylsLk%3D, PID: 9625089
-
McCrory MA, Kim HR, Wright NC, Lovelady CA, Aitkens S, Kilmer DD. Energy expenditure, physical activity, and body composition of ambulatory adults with hereditary neuromuscular disease. Am J Clin Nutr. 1998;67(6):1162–9.
-
(1998)
Am J Clin Nutr
, vol.67
, Issue.6
, pp. 1162-1169
-
-
McCrory, M.A.1
Kim, H.R.2
Wright, N.C.3
Lovelady, C.A.4
Aitkens, S.5
Kilmer, D.D.6
-
137
-
-
0032868977
-
Short-term aerobic training response in chronic myopathies
-
COI: 1:STN:280:DyaK1MzosVehsQ%3D%3D, PID: 10454720
-
Taivassalo T, De Stefano N, Chen J, Karpati G, Arnold D, Argov Z. Short-term aerobic training response in chronic myopathies. Muscle Nerve. 1999;22(9):1239–43.
-
(1999)
Muscle Nerve
, vol.22
, Issue.9
, pp. 1239-1243
-
-
Taivassalo, T.1
De Stefano, N.2
Chen, J.3
Karpati, G.4
Arnold, D.5
Argov, Z.6
-
138
-
-
0033986646
-
Aerobic capacity in adult dermatomyositis/polymyositis patients and healthy controls
-
COI: 1:STN:280:DC%2BD3c7gt1Cjtw%3D%3D, PID: 10638867
-
Wiesinger GF, Quittan M, Nuhr M, et al. Aerobic capacity in adult dermatomyositis/polymyositis patients and healthy controls. Arch Phys Med Rehabil. 2000;81(1):1–5.
-
(2000)
Arch Phys Med Rehabil
, vol.81
, Issue.1
, pp. 1-5
-
-
Wiesinger, G.F.1
Quittan, M.2
Nuhr, M.3
-
139
-
-
68549110457
-
Improvement in aerobic capacity after an exercise program in sporadic inclusion body myositis
-
PID: 19494728
-
Johnson LG, Collier KE, Edwards DJ, et al. Improvement in aerobic capacity after an exercise program in sporadic inclusion body myositis. J Clin Neuromuscul Dis. 2009;10(4):178–84.
-
(2009)
J Clin Neuromuscul Dis
, vol.10
, Issue.4
, pp. 178-184
-
-
Johnson, L.G.1
Collier, K.E.2
Edwards, D.J.3
-
141
-
-
84908314789
-
The effects of high intensity interval training on clinical symptoms and functional capacity in adults with neuromuscular disease
-
Jones K, Whittaker R, Miller J, Jakovljevic D, Turnbull D, Gorman G. The effects of high intensity interval training on clinical symptoms and functional capacity in adults with neuromuscular disease. J Neurol Neurosurg Psychiatry. 2013;84(11):e2.
-
(2013)
J Neurol Neurosurg Psychiatry
, vol.84
, Issue.11
, pp. e2
-
-
Jones, K.1
Whittaker, R.2
Miller, J.3
Jakovljevic, D.4
Turnbull, D.5
Gorman, G.6
-
142
-
-
68349101194
-
An exploratory study of physical activity and perceived barriers to exercise in ambulant people with neuromuscular disease compared with unaffected controls
-
PID: 19506002
-
Phillips M, Flemming N, Tsintzas K. An exploratory study of physical activity and perceived barriers to exercise in ambulant people with neuromuscular disease compared with unaffected controls. Clin Rehabil. 2009;23(8):746–55.
-
(2009)
Clin Rehabil
, vol.23
, Issue.8
, pp. 746-755
-
-
Phillips, M.1
Flemming, N.2
Tsintzas, K.3
-
143
-
-
84919818947
-
-
Wallace A, Dewar L, Skorupinska M, et al. Evaluating the benefits of community based aerobic training on the physical health and well-being of people with neuromuscular diseases: a pilot study. J Peripher Nerv Syst. 2013;18(S2)
-
Wallace A, Dewar L, Skorupinska M, et al. Evaluating the benefits of community based aerobic training on the physical health and well-being of people with neuromuscular diseases: a pilot study. J Peripher Nerv Syst. 2013;18(S2).
-
-
-
|