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Neurological Research
A Journal of Progress in Neurosurgery, Neurology and Neurosciences
Volume 42, 2020 - Issue 2
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ORIGINAL RESEARCH PAPER

Lower limb muscle magnetic resonance imaging in Chinese patients with myotonic dystrophy type 1

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Pages 170-177 | Received 29 Oct 2019, Accepted 12 Jan 2020, Published online: 17 Jan 2020

References

  • Cote C, Hiba B, Hebert LJ, et al. MRI of tibialis anterior skeletal muscle in myotonic dystrophy type 1. Can J Neurol Sci. 2011;38:112–118.
  • Park D, Lee SH, Shin JH, et al. Lower limb muscle magnetic resonance imaging in myotonic dystrophy type 1 correlates with the six-minute walk test and CTG repeats. Neuromuscul Disord. 2018;28:29–37.
  • Baroni A, Neaga I, Delbosc N, et al. Bioactive aliphatic polycarbonates carrying guanidinium functions: an innovative approach for myotonic dystrophy type 1 therapy. ACS Omega. 2019;4:18126–18135.
  • Johnson NE. Myotonic muscular dystrophies. Continuum (Minneap Minn). 2019;25:1682–1695.
  • Wenninger S, Montagnese F, Schoser B. Core clinical phenotypes in myotonic dystrophies. Front Neurol. 2018;9:303.
  • Meola G, Cardani R. Myotonic dystrophies: an update on clinical aspects, genetic, pathology, and molecular pathomechanisms. Biochim Biophys Acta. 2015;1852:594–606.
  • Diaz-Manera J, Fernandez-Torron R, LLauger J, et al. Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials. J Neurol Neurosurg Psychiatry. 2018;89:1071–1081.
  • Park JS, Park D. Five-year serial follow-up of muscle MRI in adult onset myotonic dystrophy type 1: a case report. Medicine (Baltimore). 2018;97:e9379.
  • Regula JU, Jestaedt L, Jende F, et al. Clinical muscle testing compared with whole-body magnetic resonance imaging in facio-scapulo-humeral muscular dystrophy. Clin Neuroradiol. 2016;26:445–455.
  • Zhao Y, Liu X, Zhang W, et al. Childhood autoimmune necrotizing myopathy with anti-signal recognition particle antibodies. Muscle Nerve. 2017;56:1181–1187.
  • Castillo J, Pumar JM, Rodriguez JR, et al. Magnetic resonance imaging of muscles in myotonic dystrophy. Eur J Radiol. 1993;17:141–144.
  • Hamano T, Kawamura Y, Mutoh T, et al. Muscle MRI in myotonic dystrophy type 1 with foot drop. Eur Neurol. 2010;63:144–148.
  • Kornblum C, Lutterbey G, Bogdanow M, et al. Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2: a whole body highfield MRI study. J Neurol. 2006;253:753–761.
  • Peric S, Maksimovic R, Banko B, et al. Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies. J Neurol. 2017;264:1899–1908.
  • Mathieu J, Boivin H, Meunier D, et al. Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy. Neurology. 2001;56:336–340.
  • Paoletti M, Pichiecchio A, Cotti Piccinelli S, et al. Advances in quantitative imaging of genetic and acquired myopathies: clinical applications and perspectives. Front Neurol. 2019;10:78.
  • Hu Z, Zhu Y, Liu X, et al. FHL1-related clinical, muscle MRI and genetic features in six Chinese patients with reducing body myopathy. J Hum Genet. 2019;64:919–926.
  • Li GD, Liang YY, Xu P, et al. Diffusion-tensor imaging of thigh muscles in duchenne muscular dystrophy: correlation of apparent diffusion coefficient and fractional anisotropy values with fatty infiltration. AJR Am J Roentgenol. 2016;206:867–870.
  • Xie Z, Xie Z, Yu M, et al. Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex. Orphanet J Rare Dis. 2019;14:250.
  • Yu M, Zhu Y, Xie Z, et al. Novel TTN mutations and muscle imaging characteristics in congenital titinopathy. Ann Clin Transl Neurol. 2019;6:1311–1318.
  • Zhao J, Wang Z, Hong D, et al. Mutational spectrum and clinical features in 35 unrelated mainland Chinese patients with GNE myopathy. J Neurol Sci. 2015;354:21–26.
  • Tasca G, Monforte M, Diaz-Manera J, et al. MRI in sarcoglycanopathies: a large international cohort study. J Neurol Neurosurg Psychiatry. 2018;89:72–77.
  • Feng X, Luo S, Li J, et al. Fatty infiltration evaluation and selective pattern characterization of lower limbs in limb-girdle muscular dystrophy type 2A by muscle magnetic resonance imaging. Muscle Nerve. 2018;58:536–541.
  • Fatehi F, Salort-Campana E, Le Troter A, et al. Muscle MRI of facioscapulohumeral dystrophy (FSHD): a growing demand and a promising approach. Rev Neurol (Paris). 2016;172:566–571.

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