메뉴 건너뛰기




Volumn 85, Issue 21, 2015, Pages 1886-1893

Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy

Author keywords

[No Author keywords available]

Indexed keywords

STEROID;

EID: 84947998222     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0000000000002147     Document Type: Article
Times cited : (39)

References (39)
  • 1
    • 84890805770 scopus 로고    scopus 로고
    • Eteplirs-en for the treatment of Duchenne muscular dystrophy
    • Mendell JR, Rodino-Klapac LR, Sahenk Z, et al. Eteplirs-en for the treatment of Duchenne muscular dystrophy. Ann Neurol 2013;74:637-647.
    • (2013) Ann Neurol , vol.74 , pp. 637-647
    • Mendell, J.R.1    Rodino-Klapac, L.R.2    Sahenk, Z.3
  • 2
    • 84868377982 scopus 로고    scopus 로고
    • Novel approaches to corticosteroid treatment in Duchenne muscular dystrophy
    • Hoffman EP, Reeves E, Damsker J, et al. Novel approaches to corticosteroid treatment in Duchenne muscular dystrophy. Phys Med Rehabil Clin N Am 2012;23:821-828.
    • (2012) Phys Med Rehabil Clin N Am , vol.23 , pp. 821-828
    • Hoffman, E.P.1    Reeves, E.2    Damsker, J.3
  • 3
    • 84892581676 scopus 로고    scopus 로고
    • Phase 2a study of ataluren-mediated dystrophin production in patients with nonsense mutation Duchenne muscular dystrophy
    • Finkel RS, Flanigan KM, Wong B, et al. Phase 2a study of ataluren-mediated dystrophin production in patients with nonsense mutation Duchenne muscular dystrophy. PLoS One 2013;8 e81302.
    • (2013) PLoS One , vol.8 , pp. e81302
    • Finkel, R.S.1    Flanigan, K.M.2    Wong, B.3
  • 4
    • 84947999708 scopus 로고    scopus 로고
    • ClinicalTrials.gov Accessed February 20, 2015
    • ClinicalTrials.gov. Available at: www.Clinicaltrials.gov. Accessed February 20, 2015.
  • 5
    • 79955158683 scopus 로고    scopus 로고
    • Systemic administration of PRO051 in Duchenne's muscular dystrophy
    • Goemans NM, Tulinius M, van den Akker JT, et al. Systemic administration of PRO051 in Duchenne's muscular dystrophy. N Engl J Med 2011;364:1513-1522.
    • (2011) N Engl J Med , vol.364 , pp. 1513-1522
    • Goemans, N.M.1    Tulinius, M.2    Van Den Akker, J.T.3
  • 6
    • 84889884673 scopus 로고    scopus 로고
    • Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy
    • Govoni A, Magri F, Brajkovic S, et al. Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy. Cell Mol Life Sci 2013;70:4585-4602.
    • (2013) Cell Mol Life Sci , vol.70 , pp. 4585-4602
    • Govoni, A.1    Magri, F.2    Brajkovic, S.3
  • 7
    • 58149173164 scopus 로고    scopus 로고
    • Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: Cardiac protection and improved exercise performance
    • Buyse GM, Van der Mieren G, Erb M, et al. Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance. Eur Heart J 2009;30:116-124.
    • (2009) Eur Heart J , vol.30 , pp. 116-124
    • Buyse, G.M.1    Van Der Mieren, G.2    Erb, M.3
  • 8
    • 79956111449 scopus 로고    scopus 로고
    • Idebe-none as a novel, therapeutic approach for Duchenne muscular dystrophy: Results from a 12 month, double-blind, randomized placebo-controlled trial
    • Buyse GM, Goemans N, van den Hauwe M, et al. Idebe-none as a novel, therapeutic approach for Duchenne muscular dystrophy: results from a 12 month, double-blind, randomized placebo-controlled trial. Neuromuscul Disord 2011;21:396-405.
    • (2011) Neuromuscul Disord , vol.21 , pp. 396-405
    • Buyse, G.M.1    Goemans, N.2    Van Den Hauwe, M.3
  • 9
    • 84947999709 scopus 로고    scopus 로고
    • European Medicines Agency Accessed February 20, 2015
    • European Medicines Agency. Available at: www.ema. europa.eu. Accessed February 20, 2015.
  • 10
    • 68249155413 scopus 로고    scopus 로고
    • Endomysial fibro-sis in Duchenne muscular dystrophy: A marker of poor outcome associated with macrophage alternative activation
    • Desguerre I, Mayer M, Leturcq F, et al. Endomysial fibro-sis in Duchenne muscular dystrophy: a marker of poor outcome associated with macrophage alternative activation. J Neuropathol Exp Neurol 2009;68:762-773.
    • (2009) J Neuropathol Exp Neurol , vol.68 , pp. 762-773
    • Desguerre, I.1    Mayer, M.2    Leturcq, F.3
  • 11
    • 0014353260 scopus 로고
    • Histopathological changes in Duchenne muscular dystrophy
    • Bell CB, Conen PE. Histopathological changes in Duchenne muscular dystrophy. J Neurol Sci 1968;7:529-540.
    • (1968) J Neurol Sci , vol.7 , pp. 529-540
    • Bell, C.B.1    Conen, P.E.2
  • 13
    • 0031669150 scopus 로고    scopus 로고
    • Sarcoglycan deficiency in large Italian population of myopathic patients
    • Prelle A, Comi GP, Tancredi L, et al. Sarcoglycan deficiency in large Italian population of myopathic patients. Acta Neuropathol 1998;96:509-514.
    • (1998) Acta Neuropathol , vol.96 , pp. 509-514
    • Prelle, A.1    Comi, G.P.2    Tancredi, L.3
  • 14
    • 0029145660 scopus 로고
    • Repro-ducibility of plasma hormone levels in postmenopausal women over a two to three year period
    • Hankinson SE, Manson JE, Spiegelman D, et al. Repro-ducibility of plasma hormone levels in postmenopausal women over a two to three year period. Cancer Epidemiol Biomarkers Prev 1995;4:649-654.
    • (1995) Cancer Epidemiol Biomarkers Prev , vol.4 , pp. 649-654
    • Hankinson, S.E.1    Manson, J.E.2    Spiegelman, D.3
  • 15
    • 33644522383 scopus 로고    scopus 로고
    • Facioscapu-lohumeral muscular dystrophy in mice overexpressing FRG1
    • Gabellini D, D'Antona G, Moggio M, et al. Facioscapu-lohumeral muscular dystrophy in mice overexpressing FRG1. Nature 2006;439:973-977.
    • (2006) Nature , vol.439 , pp. 973-977
    • Gabellini, D.1    D'Antona, G.2    Moggio, M.3
  • 16
    • 84920677763 scopus 로고    scopus 로고
    • A phase 1/2a folli-statin gene therapy trial for Becker muscular dystrophy
    • Mendel J, Sahenk Z, Malik1 V, et al. A phase 1/2a folli-statin gene therapy trial for Becker muscular dystrophy. Mol Ther 2015;23:192-201.
    • (2015) Mol Ther , vol.23 , pp. 192-201
    • Mendel, J.1    Sahenk, Z.2    Malik, V.3
  • 17
    • 36048945922 scopus 로고    scopus 로고
    • ImageJ for microscopy
    • Collins TJ. ImageJ for microscopy. Biotechniques 2007;43 (1 suppl):25-30.
    • (2007) Biotechniques , vol.43 , Issue.1 , pp. 25-30
    • Collins, T.J.1
  • 18
    • 84861882918 scopus 로고    scopus 로고
    • Quantitative paraspinal muscle measurements: Inter-software reliability and agreement using OsiriX and ImageJ
    • Fortin M, Battié MC. Quantitative paraspinal muscle measurements: inter-software reliability and agreement using OsiriX and ImageJ. Phys Ther 2012;92:853-864.
    • (2012) Phys Ther , vol.92 , pp. 853-864
    • Fortin, M.1    Battié, M.C.2
  • 19
    • 0026637764 scopus 로고
    • Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): Evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers
    • Klein CJ, Coovert DD, Bulman DE, Ray PN, Mendell JR, Burghes AH. Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers. Am J Hum Genet 1992;50:950-959.
    • (1992) Am J Hum Genet , vol.50 , pp. 950-959
    • Klein, C.J.1    Coovert, D.D.2    Bulman, D.E.3    Ray, P.N.4    Mendell, J.R.5    Burghes, A.H.6
  • 20
    • 0028910144 scopus 로고
    • Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin
    • Thanh LT, Nguyen TM, Helliwell TR, Morris GE. Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin. Am J Hum Genet 1995;56:725-731.
    • (1995) Am J Hum Genet , vol.56 , pp. 725-731
    • Thanh, L.T.1    Nguyen, T.M.2    Helliwell, T.R.3    Morris, G.E.4
  • 21
    • 0028816844 scopus 로고
    • PCR and immu-nocytochemical analyses of dystrophin-positive fibers in Duchenne muscular dystrophy
    • Uchino M, Tokunaga M, Mita S, et al. PCR and immu-nocytochemical analyses of dystrophin-positive fibers in Duchenne muscular dystrophy. J Neurol Sci 1995;129: 44-50.
    • (1995) J Neurol Sci , vol.129 , pp. 44-50
    • Uchino, M.1    Tokunaga, M.2    Mita, S.3
  • 22
    • 0026703748 scopus 로고
    • Prevalence of dystrophin positive fibers in 85 Duchenne muscular dystrophy patients
    • Fanin M, Danieli GA, Vitiello L, Senter L, Angelini C. Prevalence of dystrophin positive fibers in 85 Duchenne muscular dystrophy patients. Neuromuscul Disord 1992; 2:41-45.
    • (1992) Neuromuscul Disord , vol.2 , pp. 41-45
    • Fanin, M.1    Danieli, G.A.2    Vitiello, L.3    Senter, L.4    Angelini, C.5
  • 23
    • 77952010104 scopus 로고    scopus 로고
    • Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: Implication for clinical trials
    • Arechavala-Gomeza V, Kinali M, Feng L, et al. Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trials. Neuromuscul Disord 2010;20:295-301.
    • (2010) Neuromuscul Disord , vol.20 , pp. 295-301
    • Arechavala-Gomeza, V.1    Kinali, M.2    Feng, L.3
  • 24
    • 0017601373 scopus 로고
    • Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy
    • Emery AE. Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy. Nature 1977; 266:472-473.
    • (1977) Nature , vol.266 , pp. 472-473
    • Emery, A.E.1
  • 25
    • 0016204312 scopus 로고
    • Muscle histology in fetuses at risk for Duchenne muscular dystrophy
    • Toop J, Emery AE. Muscle histology in fetuses at risk for Duchenne muscular dystrophy. Clin Genet 1974;5:230-233.
    • (1974) Clin Genet , vol.5 , pp. 230-233
    • Toop, J.1    Emery, A.E.2
  • 26
    • 84882574534 scopus 로고    scopus 로고
    • Epigenetic control of skeletal muscle regeneration integrating genetic determinants and environmental changes
    • Giordani L, Puri PL. Epigenetic control of skeletal muscle regeneration integrating genetic determinants and environmental changes. FEBS J 2013;280:4014-4025.
    • (2013) FEBS J , vol.280 , pp. 4014-4025
    • Giordani, L.1    Puri, P.L.2
  • 27
    • 79957467268 scopus 로고    scopus 로고
    • Sculpting chromatin beyond the double helix: Epigenetic control of skeletal myogenesis
    • Sartorelli V, Juan AH. Sculpting chromatin beyond the double helix: epigenetic control of skeletal myogenesis. Curr Top Dev Biol 2011;96:57-83.
    • (2011) Curr Top Dev Biol , vol.96 , pp. 57-83
    • Sartorelli, V.1    Juan, A.H.2
  • 28
    • 84879774966 scopus 로고    scopus 로고
    • Epigenetic regulation of skeletal muscle development and differentiation
    • Bharathy N, Ling BM, Taneja R. Epigenetic regulation of skeletal muscle development and differentiation. Subcell Biochem 2013;61:139-150.
    • (2013) Subcell Biochem , vol.61 , pp. 139-150
    • Bharathy, N.1    Ling, B.M.2    Taneja, R.3
  • 29
    • 77957357566 scopus 로고    scopus 로고
    • TNF/p38a/polycomb signalling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration
    • Palacios D, Mozzetta C, Consalvi S, et al. TNF/p38a/polycomb signalling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration. Cell Stem Cell 2010;7:455-469.
    • (2010) Cell Stem Cell , vol.7 , pp. 455-469
    • Palacios, D.1    Mozzetta, C.2    Consalvi, S.3
  • 30
    • 80052410699 scopus 로고    scopus 로고
    • Epigenetic regulation of satellite cell activation during muscle regeneration
    • Dilworth FJ, Blais A. Epigenetic regulation of satellite cell activation during muscle regeneration. Stem Cell Res Ther 2011;2:18.
    • (2011) Stem Cell Res Ther , vol.2 , pp. 18
    • Dilworth, F.J.1    Blais, A.2
  • 31
    • 33646478253 scopus 로고    scopus 로고
    • Long-term benefits of deflazacort treatment for boys with Duchenne muscular dystrophy in their second decade
    • Biggar WD, Harris VA, Eliasoph L, Alman B. Long-term benefits of deflazacort treatment for boys with Duchenne muscular dystrophy in their second decade. Neuromuscul Disord 2006;16:249-255.
    • (2006) Neuromuscul Disord , vol.16 , pp. 249-255
    • Biggar, W.D.1    Harris, V.A.2    Eliasoph, L.3    Alman, B.4
  • 32
    • 4344588135 scopus 로고    scopus 로고
    • Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; Defining the gold standards of management in the use of cortico-steroids
    • Bushby K, Muntoni F, Urtizberea A, Huges R, Griggs R. Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; defining the gold standards of management in the use of cortico-steroids. Neuromuscul Disord 2004;14:526-534.
    • (2004) Neuromuscul Disord , vol.14 , pp. 526-534
    • Bushby, K.1    Muntoni, F.2    Urtizberea, A.3    Huges, R.4    Griggs, R.5
  • 35
    • 84883055833 scopus 로고    scopus 로고
    • The 6-Minute Walk Test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study
    • McDonald CM, Henricson EK, Abresch RT, et al. The 6-Minute Walk Test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study. Muscle Nerve 2013;48:343-356.
    • (2013) Muscle Nerve , vol.48 , pp. 343-356
    • McDonald, C.M.1    Henricson, E.K.2    Abresch, R.T.3
  • 36
    • 0025801496 scopus 로고
    • Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy
    • Zatz M, Rapaport D, Vainzof M, et al. Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy. J Neurol Sci 1991;102:190-196.
    • (1991) J Neurol Sci , vol.102 , pp. 190-196
    • Zatz, M.1    Rapaport, D.2    Vainzof, M.3
  • 37
    • 84875805687 scopus 로고    scopus 로고
    • Fibroadipo-genic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice
    • Mozzetta C, Consalvi S, Saccone V, et al. Fibroadipo-genic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice. EMBO Mol Med 2013;5:626-639.
    • (2013) EMBO Mol Med , vol.5 , pp. 626-639
    • Mozzetta, C.1    Consalvi, S.2    Saccone, V.3
  • 39
    • 84891505337 scopus 로고    scopus 로고
    • Magnetic resonance imaging in Duchenne muscular dystrophy: Longitudinal assessment of natural history over 18 months
    • Hollingsworth KG, Garrood P, Eagle M, Bushby K, Straub V. Magnetic resonance imaging in Duchenne muscular dystrophy: longitudinal assessment of natural history over 18 months. Muscle Nerve 2013;48:586-588.
    • (2013) Muscle Nerve , vol.48 , pp. 586-588
    • Hollingsworth, K.G.1    Garrood, P.2    Eagle, M.3    Bushby, K.4    Straub, V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.