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Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle

  • Jonathan Ennis (a1), David A. Dyment (a2), Jean Michaud (a3) and Hugh J. McMillan (a4)
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Copyright

Corresponding author

Correspondence to: Hugh J. McMillan, Division of Neurology, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, ON, K1H 8L1. Email: hmcmillan@cheo.on.ca

References

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1. Ryan, MM, Schnell, C, Strickland, CD, Shield, LK, Morgan, G, Iannanccone, ST, et al. Nemaline myopathy: a clinical study of 143 cases. Ann Neurol. 2001;50:312-320.
2. Laing, NG, Dye, DE, Wallgren-Pettersson, C, Richard, G, Monnier, N, Lillis, S, et al. Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1). Hum Mut. 2009;30:1267-1277.
3. Agrawal, PB, Strickland, CD, Midgett, C, Morales, A, Newburger, DE, Poulos, MA, et al. Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations. Ann Neurol. 2004;56:86-96.
4. Castiglioni, C, Cassandrini, D, Fattori, F, Bellacchio, E, D’Amico, A, Alvarez, K, et al. Muscle magnetic resonance imaging and histopathology in ACTA1-related congenital nemaline myopathy. Muscle Nerve. 2014;50:1011-1016.
5. Jungbluth, H, Sewry, CA, Counsell, S, Allsop, J, Chattopadhyay, A, Mercuri, E. Magnetic resonance imaging of muscle in nemaline myopathy. Neuromusc Disord. 2004;14:779-784.

Keywords

Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle

  • Jonathan Ennis (a1), David A. Dyment (a2), Jean Michaud (a3) and Hugh J. McMillan (a4)

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