-
1
-
-
0034098406
-
Prevalence of sporadic inclusion body myositis in Western Australia
-
DOI 10.1002/(SICI)1097-4598(200006)23:6<970::AID-MUS20>3.0.CO;2-I
-
Phillips BA, Zilko PJ, Mastaglia FL. Prevalence of sporadic inclusion body myositis in Western Australia. Muscle Nerve. 2000;23(6):970-2. (Pubitemid 30354508)
-
(2000)
Muscle and Nerve
, vol.23
, Issue.6
, pp. 970-972
-
-
Phillips, B.A.1
Zilko, P.J.2
Mastaglia, F.L.3
-
2
-
-
0024340503
-
Inclusion body myositis. Observations in 40 patients
-
Lotz BP, Engel AG, Nishino H, Stevens JC, Litch WJ. Inclusion body myositis. Observations in 40 patients. Brain. 1989;112(Pt 3):727-47. (Pubitemid 19151167)
-
(1989)
Brain
, vol.112
, Issue.3
, pp. 727-747
-
-
Lotz, B.P.1
Engel, A.G.2
Nishino, H.3
Stevens, J.C.4
Litchy, W.J.5
-
3
-
-
29144533183
-
Inclusion body myositis: Clinical features and clinical course of the disease in 64 patients
-
DOI 10.1007/s00415-005-0884-y
-
Badrising UA, Maat-Schieman ML, van Houwelingen JC, et al. Inclusion body myositis. Clinical features and clinical course of the disease in 64 patients. Neurology. 2005;252(12):1448-54. (Pubitemid 41803832)
-
(2005)
Journal of Neurology
, vol.252
, Issue.12
, pp. 1448-1454
-
-
Badrising, U.A.1
Maat-Schieman, M.L.C.2
Van Houwelingen, J.C.3
Van Doorn, P.A.4
Van Duinen, S.G.5
Van Engelen, B.G.M.6
Faber, C.G.7
Hoogendijk, J.E.8
De Jager, A.E.9
Koehler, P.J.10
De Visser, M.11
Verschuuren, J.J.G.M.12
Wintzen, A.R.13
-
4
-
-
40649124555
-
Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota
-
Wilson FC, Ytterberg SR, St Sauver JL, et al. Epidemiology of sporadic inclusion body myositis and polymyositis in Olmsted County, Minnesota. J Rheumatol. 2008;35(3):445-7. (Pubitemid 351374418)
-
(2008)
Journal of Rheumatology
, vol.35
, Issue.3
, pp. 445-447
-
-
Wilson, F.C.1
Ytterberg, S.R.2
St. Sauver, J.L.3
Reed, A.M.4
-
5
-
-
0029957253
-
Inclusion body myositis: Clinical and pathological boundaries
-
10.1002/ana.410400407
-
Amato AA, Gronseth GS, Jackson, et al. Inclusion body myositis: clinical and pathological boundaries. Ann Neurol. 1995;40:581-6.
-
(1995)
Ann Neurol
, vol.40
, pp. 581-586
-
-
Amato, A.A.1
Gronseth, G.S.2
Jackson3
-
7
-
-
0034649445
-
Epidemiology of inclusion body myositis in the Netherlands: A nationwide study
-
11087787 10.1212/WNL.55.9.1385 1:STN:280:DC%2BD3M%2FlvFyntQ%3D%3D
-
Badrising UA, Maat-Schieman M, van Duinen SG, et al. Epidemiology of inclusion body myositis in The Netherlands: a nationwide study. Neurology. 2000;55:1385-7.
-
(2000)
Neurology
, vol.55
, pp. 1385-1387
-
-
Badrising, U.A.1
Maat-Schieman, M.2
Van Duinen, S.G.3
-
8
-
-
0028258354
-
Inclusion body myositis: Clinical, morphological, physiological and laboratory findings in 18 cases
-
Lindberg C, Persson LI, Bjorkander J, Oldfors A. Inclusion body myositis: clinical, morphological, physiological, and laboratory findings in 18 cases. Acta Neurol Scand. 1994;89:123-31. (Pubitemid 24095268)
-
(1994)
Acta Neurologica Scandinavica
, vol.89
, Issue.2
, pp. 123-131
-
-
Lindberg, C.1
Persson, L.2
Bjorkander, J.3
Oldfors, A.4
-
9
-
-
0026702459
-
Inclusion body myositis: Analysis of 32 cases
-
1331441 1:STN:280:DyaK3s%2FlvFSjtA%3D%3D
-
Sayers ME, Chou SM, Calabrese LH. Inclusion body myositis: analysis of 32 cases. J Rheumatol. 1992;19:1385-9.
-
(1992)
J Rheumatol
, vol.19
, pp. 1385-1389
-
-
Sayers, M.E.1
Chou, S.M.2
Calabrese, L.H.3
-
10
-
-
50449098865
-
Sporadic inclusion body myositis: Phenotypic variability, and influence of HLA-DR3 in a cohort of 57 Australian cases
-
18258695 10.1136/jnnp.2007.138891 1:STN:280:DC%2BD1critVKhuw%3D%3D
-
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
-
11
-
-
0029086623
-
Inclusion body myositis: Explanation for poor response to immunosuppressive therapy
-
7617187 10.1212/WNL.45.7.1302 1:STN:280:DyaK2Mzkt1CjsQ%3D%3D
-
Barohn RJ, Amato AA, Sahenk Z, Kissel JT, Mendell JR. Inclusion body myositis: explanation for poor response to immunosuppressive therapy. Neurology. 1995;45(7):1302-4.
-
(1995)
Neurology
, vol.45
, Issue.7
, pp. 1302-1304
-
-
Barohn, R.J.1
Amato, A.A.2
Sahenk, Z.3
Kissel, J.T.4
Mendell, J.R.5
-
13
-
-
0028787389
-
Inclusion body myositis and myopathies
-
7486861 10.1002/ana.410380504 1:STN:280:DyaK28%2FnsVWrsw%3D%3D Authors of this article propose diagnostic criteria for definite and possible sporadic inclusion body myositis based on a combination of clinical features and laboratory findings including serum creatine kinase, electromyography, and muscle histopathology. This is the first major effort to define diagnostic criteria for IBM. These criteria have withstood the test of time with some additions as in reference 14
-
•• Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol. 1995;38(5):705-13. Authors of this article propose diagnostic criteria for definite and possible sporadic inclusion body myositis based on a combination of clinical features and laboratory findings including serum creatine kinase, electromyography, and muscle histopathology. This is the first major effort to define diagnostic criteria for IBM. These criteria have withstood the test of time with some additions as in reference 14.
-
(1995)
Ann Neurol.
, vol.38
, Issue.5
, pp. 705-713
-
-
Griggs, R.C.1
Askanas, V.2
Dimauro, S.3
-
14
-
-
75149122299
-
Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June, 2008
-
20074951 10.1016/j.nmd.2009.11.003 1:STN:280:DC%2BC3c%2FpsVequg%3D%3D In addition to the Griggs categories of pathologically defined IBM and possible IBM, participants of the 2008 European Neuromuscular Center workshop introduced clinically defined IBM to include IBM cases with weakness involving finger flexion more than shoulder abduction as well as knee extension more than hip flexion. The pathologic criteria for possible IBM and clinically defined IBM are invasion of non-necrotic fibers by mononuclear cells, or rimmed vacuoles, or increased MHC-1 expression on the surface of muscle fibers. This facilitates the diagnosis of patients who fulfill clinical criteria for IBM but do not have the pathologic features set forth by Griggs et al
-
•• Hilton-Jones D, Miller A, Parton M, et al. Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June, 2008. Neuromuscul Disord. 2010;20(2):142-7. In addition to the Griggs categories of pathologically defined IBM and possible IBM, participants of the 2008 European Neuromuscular Center workshop introduced clinically defined IBM to include IBM cases with weakness involving finger flexion more than shoulder abduction as well as knee extension more than hip flexion. The pathologic criteria for possible IBM and clinically defined IBM are invasion of non-necrotic fibers by mononuclear cells, or rimmed vacuoles, or increased MHC-1 expression on the surface of muscle fibers. This facilitates the diagnosis of patients who fulfill clinical criteria for IBM but do not have the pathologic features set forth by Griggs et al.
-
(2010)
Neuromuscul Disord.
, vol.20
, Issue.2
, pp. 142-147
-
-
Hilton-Jones, D.1
Miller, A.2
Parton, M.3
-
15
-
-
70349658621
-
Inclusion body myositis: Old and new concepts
-
19864656 10.1136/jnnp.2009.173823 1:STN:280:DC%2BD1Mjit1Ohtg%3D%3D
-
Amato AA, Barohn RJ. Inclusion body myositis: old and new concepts. J Neurol Neurosurg Psychiatry. 2009;80(11):1186-93.
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, Issue.11
, pp. 1186-1193
-
-
Amato, A.A.1
Barohn, R.J.2
-
16
-
-
0028072558
-
HLA associations with inclusion body myositis
-
Garlepp MJ, Laing B, Zilko PJ, et al. HLA associations with inclusion body myositis. Clin Exp Immunol. 1994;98:40-5. (Pubitemid 24315449)
-
(1994)
Clinical and Experimental Immunology
, 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
-
17
-
-
78549272011
-
Morphologic imaging in muscular dystrophies and inflammatory myopathies
-
20449587 10.1007/s00256-010-0930-4
-
Degardin A, Morillon D, Lacour A, Cotten A, Vermersch P, Stojkovic T. Morphologic imaging in muscular dystrophies and inflammatory myopathies. Skeletal Radiol. 2010;39(12):1219-27.
-
(2010)
Skeletal Radiol
, vol.39
, Issue.12
, pp. 1219-1227
-
-
Degardin, A.1
Morillon, D.2
Lacour, A.3
Cotten, A.4
Vermersch, P.5
Stojkovic, T.6
-
18
-
-
82155172633
-
Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis
-
21288962 10.1093/rheumatology/ker001
-
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.
-
(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
-
19
-
-
80051480260
-
Increased [11C]PIB-PET levels in inclusion body myositis are indicative of amyloid beta deposition
-
20732867 10.1136/jnnp.2009.197640
-
Maetzler W, Reimold M, Schittenhelm J, et al. Increased [11C]PIB-PET levels in inclusion body myositis are indicative of amyloid beta deposition. J Neurol Neurosurg Psychiatry. 2011;82(9):1060-2.
-
(2011)
J Neurol Neurosurg Psychiatry
, vol.82
, Issue.9
, pp. 1060-1062
-
-
Maetzler, W.1
Reimold, M.2
Schittenhelm, J.3
-
20
-
-
40349098675
-
Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM
-
17881720 10.1212/01.wnl.0000277527.69388.fe
-
Chahin N, Engel AG. Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM. Neurology. 2008;70(6):418-24.
-
(2008)
Neurology.
, vol.70
, Issue.6
, pp. 418-424
-
-
Chahin, N.1
Engel, A.G.2
-
21
-
-
0034981219
-
Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositis
-
DOI 10.1016/S0960-8966(00)00219-4, PII S0960896600002194
-
Van der Meulen MF, Hoogendijk JE, Moons KG, Veldman H, Badrising UA, Wokke JH. Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositis. Neuromuscul Disord. 2001;11:447-51. (Pubitemid 32510004)
-
(2001)
Neuromuscular Disorders
, vol.11
, Issue.5
, pp. 447-451
-
-
Van Der Meulen, M.F.G.1
Hoogendijk, J.E.2
Moons, K.G.M.3
Veldman, H.4
Badrising, U.A.5
Wokke, J.H.J.6
-
22
-
-
33845970203
-
Myeloid dendritic cells in inclusion-body myositis and polymyositis
-
DOI 10.1002/mus.20649
-
Greenberg SA, Pinkus GS, Amato AA, Pinkus JL. Myeloid dendritic cells in inclusion-body myositis and polymyositis. Muscle Nerve. 2007;35(1):17-23. (Pubitemid 46052644)
-
(2007)
Muscle and Nerve
, vol.35
, Issue.1
, pp. 17-23
-
-
Greenberg, S.A.1
Pinkus, G.S.2
Amato, A.A.3
Pinkus, J.L.4
-
23
-
-
82955195402
-
Inclusion body myositis
-
21885973 10.1097/BOR.0b013e32834b53cc
-
Greenberg SA. Inclusion body myositis. Curr Opin Rheumatol. 2011;23(6):574-8.
-
(2011)
Curr Opin Rheumatol
, vol.23
, Issue.6
, pp. 574-578
-
-
Greenberg, S.A.1
-
24
-
-
0037159180
-
Molecular profiles of inflammatory myopathies
-
Greenberg SA, Sanoudou D, Haslett JN, et al. Molecular profiles of inflammatory myopathies. Neurology. 2002;59(8):1170-82. (Pubitemid 35192386)
-
(2002)
Neurology
, vol.59
, Issue.8
, pp. 1170-1182
-
-
Greenberg, S.A.1
Sanoudou, D.2
Haslett, J.N.3
Kohane, I.S.4
Kunkel, L.M.5
Beggs, A.H.6
Amato, A.A.7
-
25
-
-
33645086701
-
Plasma cells in muscle in inclusion body myositis and polymyositis
-
16344523 10.1212/01.wnl.0000187124.92826.20 1:STN:280: DC%2BD2Mnmt1GntA%3D%3D
-
Greenberg SA, Bradshaw EM, Pinkus JL, et al. Plasma cells in muscle in inclusion body myositis and polymyositis. Neurology. 2005;65(11):1782-7.
-
(2005)
Neurology
, vol.65
, Issue.11
, pp. 1782-1787
-
-
Greenberg, S.A.1
Bradshaw, E.M.2
Pinkus, J.L.3
-
26
-
-
79956350423
-
Autoantibodies against a 43 kDa muscle protein in inclusion body myositis
-
21629782 10.1371/journal.pone.0020266 1:CAS:528:DC%2BC3MXmslCqs7Y%3D Since microarray studies reported abundant immunoglobulin gene transcripts in IBM muscle derived from local abundant plasma cells, this provided a rationale for searching for circulating autoantibodies. Imunoblots against normal human muscle demonstrate that 52 % of IBM patient samples recognized a 43 kDa muscle protein. None of those with other diseases or healthy volunteers had this protein
-
• Salajegheh M, Lam T, Greenberg SA. Autoantibodies against a 43 kDa muscle protein in inclusion body myositis. PLoS One. 2011;6:e20266. Since microarray studies reported abundant immunoglobulin gene transcripts in IBM muscle derived from local abundant plasma cells, this provided a rationale for searching for circulating autoantibodies. Imunoblots against normal human muscle demonstrate that 52 % of IBM patient samples recognized a 43 kDa muscle protein. None of those with other diseases or healthy volunteers had this protein.
-
(2011)
PLoS One
, vol.6
, pp. 20266
-
-
Salajegheh, M.1
Lam, T.2
Greenberg, S.A.3
-
27
-
-
33644869497
-
Inclusion-body myositis: A myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition
-
16432144 10.1212/01.wnl.0000192128.13875.1e 1:CAS:528: DC%2BD28Xht1Krtw%3D%3D
-
Askanas V, Engel WK. Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition. Neurology. 2006;66(2 Suppl 1):S39-48.
-
(2006)
Neurology
, vol.66
, Issue.2 SUPPL. 1
-
-
Askanas, V.1
Engel, W.K.2
-
28
-
-
33845217281
-
AβPP-overexpression and proteasome inhibition increase αB-crystallin in cultured human muscle: Relevance to inclusion-body myositis
-
DOI 10.1016/j.nmd.2006.08.009, PII S0960896606005189
-
Wojcik S, Engel WK, McFerrin J, Paciello O, Askanas V. AbetaPP-overexpression and proteasome inhibition increase alpha B-crystallin in cultured human muscle: relevance to inclusion-body myositis. Neuromuscul Disord. 2006;16(12):839-44. (Pubitemid 44855597)
-
(2006)
Neuromuscular Disorders
, vol.16
, Issue.12
, pp. 839-844
-
-
Wojcik, S.1
Engel, W.K.2
McFerrin, J.3
Paciello, O.4
Askanas, V.5
-
29
-
-
79953792495
-
Sporadic inclusion-body myositis: Conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau
-
21392932 10.1016/j.lpm.2010.11.024
-
Askanas V, Engel WK. Sporadic inclusion-body myositis: conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau. Presse Med. 2011;40(4 Pt 2):e219-35.
-
(2011)
Presse Med
, vol.40
, Issue.4 PART 2
-
-
Askanas, V.1
Engel, W.K.2
-
30
-
-
70349322489
-
Nature of "tau" immunoreactivity in normal myonuclei and inclusion body myositis
-
19626672 10.1002/mus.21471 1:CAS:528:DC%2BD1MXhtlCgurvI
-
Salajegheh M, Pinkus JL, Nazareno R, et al. Nature of "Tau" immunoreactivity in normal myonuclei and inclusion body myositis. Muscle Nerve. 2009;40(4):520-8.
-
(2009)
Muscle Nerve
, vol.40
, Issue.4
, pp. 520-528
-
-
Salajegheh, M.1
Pinkus, J.L.2
Nazareno, R.3
-
31
-
-
78149406278
-
Novel demonstration of amyloid-β oligomers in sporadic inclusion-body myositis muscle fibers
-
20711838 10.1007/s00401-010-0737-3 1:CAS:528:DC%2BC3cXhtlSjtrfF Askanas' group reported for the first time in 2010 that IBM muscle samples had accumulation of toxic low-molecular weight amyloid β oligomers on dot-immunoblots with a variety of molecular weights and intensity but none of the control muscle biopsies had amyloid β oligomers. Nonfibrillar cytotoxic "Aβ-Derived Diffusible Ligands" originally derived from Aβ42 are prominently increased on dot-immunoblots, being consistent with the concept that intracellular toxicity of Ab42 oligomers is likely an important aspect of IBM pathogenesis. Finally, they demonstrated in cultured human muscle fibers that inhibition of autophagy is a novel cause of Aβ oligomerization
-
• Nogalska A, D'Agostino C, Engel WK, Klein WL, Askanas V. Novel demonstration of amyloid-β oligomers in sporadic inclusion-body myositis muscle fibers. Acta Neuropathol. 2010;120(5):661-6. Askanas' group reported for the first time in 2010 that IBM muscle samples had accumulation of toxic low-molecular weight amyloid β oligomers on dot-immunoblots with a variety of molecular weights and intensity but none of the control muscle biopsies had amyloid β oligomers. Nonfibrillar cytotoxic "Aβ-Derived Diffusible Ligands" originally derived from Aβ42 are prominently increased on dot-immunoblots, being consistent with the concept that intracellular toxicity of Ab42 oligomers is likely an important aspect of IBM pathogenesis. Finally, they demonstrated in cultured human muscle fibers that inhibition of autophagy is a novel cause of Aβ oligomerization.
-
(2010)
Acta Neuropathol.
, vol.120
, Issue.5
, pp. 661-666
-
-
Nogalska, A.1
D'Agostino, C.2
Engel, W.K.3
Klein, W.L.4
Askanas, V.5
-
32
-
-
67650264666
-
Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis
-
19533646 10.1002/mus.21386 1:CAS:528:DC%2BD1MXptVaqtr4%3D
-
Salajegheh M, Pinkus JL, Taylor JP, et al. Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis. Muscle Nerve. 2009;40:19-31.
-
(2009)
Muscle Nerve
, vol.40
, pp. 19-31
-
-
Salajegheh, M.1
Pinkus, J.L.2
Taylor, J.P.3
-
33
-
-
79952455882
-
Treatment-responsive polymyositis transforming into inclusion body myositis
-
Verma A, Bradley WG, Ringel SP. Treatment-responsive polymyositis transforming into inclusion body myositis. Neurology. 2008;P060.19.
-
(2008)
Neurology
-
-
Verma, A.1
Bradley, W.G.2
Ringel, S.P.3
-
34
-
-
81055125519
-
Long-term observational study of sporadic inclusion body myositis
-
21994327 10.1093/brain/awr213
-
Benveniste O, Guiguet M, Freebody J, et al. Long-term observational study of sporadic inclusion body myositis. Brain. 2011;134(Pt 11):3176-84.
-
(2011)
Brain
, vol.134
, Issue.PART 11
, pp. 3176-3184
-
-
Benveniste, O.1
Guiguet, M.2
Freebody, J.3
-
35
-
-
0027935703
-
Inclusion body myositis: Treatment with intravenous immunoglobulin
-
Amato AA, Barohn RJ, Jackson CE, Pappert EJ, Sahenk Z, Kissel JT. Inclusion body myositis: treatment with intravenous immunoglobulin. Neurology. 1994;44(8):1516-8. (Pubitemid 24247450)
-
(1994)
Neurology
, vol.44
, Issue.8
, pp. 1516-1518
-
-
Amato, A.A.1
Barohn, R.J.2
Jackson, C.E.3
Pappert, E.J.4
Sahenk, Z.5
Kissel, J.T.6
-
36
-
-
0030947027
-
Treatment of inclusion-body myositis with IVIg: A double-blind, placebo- controlled study
-
Dalakas MC, Sonies B, Dambrosia J, Sekul E, Cupler E, Sivakumar K. Treatment of inclusion-body myositis with IVIg: a double-blind, placebo-controlled study. Neurology. 1997;48:712-6. (Pubitemid 27120112)
-
(1997)
Neurology
, vol.48
, Issue.3
, pp. 712-716
-
-
Dalakas, M.C.1
Sonies, B.2
Dambrosia, J.3
Sekul, E.4
Cupler, E.5
Sivakumar, K.6
-
37
-
-
0035852876
-
A controlled study of intravenous immunoglobulin combined with prednisone in the treatment of IBM
-
Dalakas MC, Koffman B, Fujii M, Spector S, Sivakumar K, Cupler E. A controlled study of intravenous immunoglobulin combined with prednisone in the treatment of IBM. Neurology. 2001;56:323-7. (Pubitemid 32144142)
-
(2001)
Neurology
, vol.56
, Issue.3
, pp. 323-327
-
-
Dalakas, M.C.1
Koffman, B.2
Fujii, M.3
Spector, S.4
Sivakumar, K.5
Cupler, E.6
-
38
-
-
0035856461
-
Randomized pilot trial of betaINF1a (Avonex) in patients with inclusion body myositis
-
Muscle Study Group 10.1212/WNL.57.9.1566
-
Muscle Study Group. Randomized pilot trial of betaINF1a (Avonex) in patients with inclusion body myositis. Neurology. 2001;57:1566-70.
-
(2001)
Neurology
, vol.57
, pp. 1566-1570
-
-
-
39
-
-
4143058047
-
Randomized pilot trial of high-dose betaINF-1a in patients with inclusion body myositis
-
Muscle Study Group 10.1212/01.WNL.0000134675.98525.79
-
Muscle Study Group. Randomized pilot trial of high-dose betaINF-1a in patients with inclusion body myositis. Neurology. 2004;63:718-20.
-
(2004)
Neurology
, vol.63
, pp. 718-720
-
-
-
40
-
-
0036197698
-
Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo
-
DOI 10.1002/ana.10121
-
Badrising UA, Maat-Schieman ML, Ferrari, et al. Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo. Ann Neurol. 2002;51:369-72. (Pubitemid 34206293)
-
(2002)
Annals of Neurology
, vol.51
, Issue.3
, pp. 369-372
-
-
Badrising, U.A.1
Maat-Schieman, M.L.C.2
Ferrari, M.D.3
Zwinderman, A.H.4
Wessels, J.A.M.5
Breedveld, F.C.6
Van Doorn, P.A.7
Van Engelen, B.G.M.8
Hoogendijk, J.E.9
Howeler, C.J.10
De Jager, A.E.11
Jennekens, F.G.I.12
Koehler, P.J.13
De Visser, M.14
Viddeleer, A.15
Verschuuren, J.J.16
Wintzen, A.R.17
-
41
-
-
0038458498
-
Anti-T-lymphocyte globulin treatment in inclusion body myositis: A randomized pilot study
-
Lindberg C, Trysberg E, Tarkowski A, Oldfors A. Anti-T-lymphocyte globulin treatment in inclusion body myositis: a randomized pilot study. Neurology. 2003;61:260-2. (Pubitemid 36875317)
-
(2003)
Neurology
, vol.61
, Issue.2
, pp. 260-262
-
-
Lindberg, C.1
Trysberg, E.2
Tarkowski, A.3
Oldfors, A.4
-
42
-
-
0037046195
-
A pilot randomized trial of oxandrolone in inclusion body myositis
-
Rutkove SB, Parker RA, Nardin RA, Connolly CE, Felic KJ, Raynor EM. A pilot randomized trial of oxandrolone in inclusion body myositis. Neurology. 2002;58(7):1081-7. (Pubitemid 34298550)
-
(2002)
Neurology
, vol.58
, Issue.7
, pp. 1081-1087
-
-
Rutkove, S.B.1
Parker, R.A.2
Nardin, R.A.3
Connolly, C.E.4
Felice, K.J.5
Raynor, E.M.6
-
43
-
-
33644852538
-
Pilot trial of etanercept in the treatment of inclusion-body myositis
-
16432140 10.1212/01.wnl.0000192258.32408.54 1:CAS:528: DC%2BD28Xht1Kquw%3D%3D
-
Barohn RJ, Herbelin L, Kissel JT, et al. Pilot trial of etanercept in the treatment of inclusion-body myositis. Neurology. 2006;66(2 Suppl 1):S123-4.
-
(2006)
Neurology
, vol.66
, Issue.2 SUPPL. 1
-
-
Barohn, R.J.1
Herbelin, L.2
Kissel, J.T.3
-
44
-
-
67649399221
-
Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis
-
19454532 10.1093/brain/awp104
-
Dalakas MC, Rakocevic G, Schmidt J, et al. Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis. Brain. 2009;132(Pt 6):1536-44.
-
(2009)
Brain
, vol.132
, Issue.PART 6
, pp. 1536-1544
-
-
Dalakas, M.C.1
Rakocevic, G.2
Schmidt, J.3
-
45
-
-
80054715362
-
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis
-
21695654 10.1007/s10072-011-0657-6
-
Sancricca C, Mora M, Ricci E, Tonali PA, Mantegazza R, Mirabella M. Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis. Neurol Sci. 2011;32(5):841-7.
-
(2011)
Neurol Sci
, vol.32
, Issue.5
, pp. 841-847
-
-
Sancricca, C.1
Mora, M.2
Ricci, E.3
Tonali, P.A.4
Mantegazza, R.5
Mirabella, M.6
-
46
-
-
84873092074
-
Pilot Trial of lithium treatment in inclusion body myositis
-
Saperstein DS, Levine T, Hank N, Kitazawa M, Bowser R, LaFerla F. Pilot Trial of lithium treatment in inclusion body myositis. Neurology. 2011;76 Suppl 4:A106.
-
(2011)
Neurology
, vol.76
, Issue.SUPPL. 4
, pp. 106
-
-
Saperstein, D.S.1
Levine, T.2
Hank, N.3
Kitazawa, M.4
Bowser, R.5
Laferla, F.6
-
47
-
-
67749106389
-
Autophagy, lithium, and amyotrophic lateral sclerosis
-
19609902 10.1002/mus.21423 1:CAS:528:DC%2BD1MXhtVKnsb3K
-
Pasquali L, Longone P, Isidoro C, Ruggieri S, Paparelli A, Fornai F. Autophagy, lithium, and amyotrophic lateral sclerosis. Muscle Nerve. 2009;40(2):173-94.
-
(2009)
Muscle Nerve
, vol.40
, Issue.2
, pp. 173-194
-
-
Pasquali, L.1
Longone, P.2
Isidoro, C.3
Ruggieri, S.4
Paparelli, A.5
Fornai, F.6
-
48
-
-
84904309237
-
Twelve-month change of IBMFRS in the arimocolomol inclusion body myositis pilot study
-
New Orleans, LA, USA; April 26 2012. Actual page etc from Dr. Baroh's CV)
-
Wang Y, He J, McVey AL, et al. Twelve-month change of IBMFRS in the arimocolomol inclusion body myositis pilot study. Poster 7.255 presented at the American Academy of Neurology. Annual Meeting. New Orleans, LA, USA; April 26 2012. Actual page etc from Dr. Baroh's CV).
-
American Academy of Neurology. Annual Meeting
-
-
Wang, Y.1
He, J.2
McVey, A.L.3
-
49
-
-
0027378842
-
Inclusion body myositis: New concepts
-
Sekul EA, Dalakas MC. Inclusion body myositis: new concepts. Semin Neurol. 1993;13(3):256-63. (Pubitemid 23300092)
-
(1993)
Seminars in Neurology
, vol.13
, Issue.3
, pp. 256-263
-
-
Sekul, E.A.1
Dalakas, M.C.2
-
50
-
-
81055144452
-
A 12-year follow-up in sporadic inclusion body myositis: An end stage with major disabilities
-
21908393 10.1093/brain/awr217
-
Cox FM, Titulaer MJ, Sont JK, Wintzen AR, Verschuuren JJ, Badrising UA. A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities. Brain. 2011;134(Pt 11):3167-75.
-
(2011)
Brain
, vol.134
, Issue.PART 11
, pp. 3167-3175
-
-
Cox, F.M.1
Titulaer, M.J.2
Sont, J.K.3
Wintzen, A.R.4
Verschuuren, J.J.5
Badrising, U.A.6
-
51
-
-
12244300976
-
Sporadic inclusion body myositis: Pilot study on the effects of a home exercise program on muscle function, histopathology and inflammatory reaction
-
DOI 10.1080/16501970306110
-
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. (Pubitemid 36204070)
-
(2003)
Journal of Rehabilitation Medicine
, vol.35
, Issue.1
, pp. 31-35
-
-
Arnardottir, S.1
Alexanderson, H.2
Lundberg, I.E.3
Borg, K.4
-
52
-
-
34447338318
-
The effectiveness of an individualized, home-based functional exercise program for patients with sporadic inclusion body myositis
-
DOI 10.1097/CND.0b013e3181237291, PII 0013140220070600000001
-
Johnson GL, et al. The effectiveness of an individualized, home-based functional exercise program for patients with sporadic inclusion body myositis. J Clin Neuromuscul Dis. 2007;8:187-94. (Pubitemid 47052000)
-
(2007)
Journal of Clinical Neuromuscular Disease
, vol.8
, Issue.4
, pp. 187-194
-
-
Johnson, L.G.1
Edwards, D.J.2
Walters, S.3
Thickbroom, G.W.4
Mastaglia, F.L.5
-
53
-
-
68549110457
-
Improvement in aerobic capacity after an exercise program in sporadic inclusion body myositis
-
19494728 10.1097/CND.0b013e3181a23c86
-
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
|