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BioMed Research International
Volume 2015 (2015), Article ID 803148, 9 pages
http://dx.doi.org/10.1155/2015/803148
Research Article

The Quantitative Assessment of Imaging Features for the Study of Hirayama Disease Progression

Department of Orthopedics, Huashan Hospital, Fudan University, Shanghai 200040, China

Received 30 July 2015; Revised 19 September 2015; Accepted 21 September 2015

Academic Editor: Kenjiro Ono

Copyright © 2015 Minghao Shao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. K. Hirayama, Y. Toyokura, and T. Tsubaki, “Juvenile muscular atrophy of unilateral upper extremity: a new clinical entity,” Folia Psychiatrica et Neurologica Japonica, vol. 61, no. 2, pp. 2190–2197, 1959 (Japanese). View at Google Scholar
  2. K. Hirayama, M. Tomonaga, K. Kitano, T. Yamada, S. Kojima, and K. Arai, “The first autopsy case of ‘juvenile muscular atrophy of unilateral upper extremity’,” Shinkei Naika, vol. 22, no. 2, pp. 85–86, 1985. View at Google Scholar
  3. K. Hirayama, “Juvenile muscular atrophy of unilateral upper extremity (Hirayama disease)—half-century progress and establishment since its discovery,” Brain and Nerve, vol. 60, no. 1, pp. 17–29, 2008. View at Google Scholar · View at Scopus
  4. M. Kohno, H. Takahashi, A. Yagishita, and H. Tanabe, “‘Disproportion theory’ of the cervical spine and spinal cord in patients with juvenile cervical flexion myelopathy. A study comparing cervical magnetic resonance images with those of normal controls,” Surgical Neurology, vol. 50, no. 5, pp. 421–430, 1998. View at Publisher · View at Google Scholar · View at Scopus
  5. Y.-C. Huang, L.-S. Ro, H.-S. Chang et al., “A clinical study of Hirayama disease in Taiwan,” Muscle and Nerve, vol. 37, no. 5, pp. 576–582, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. Y. Li and K. Remmel, “A case of monomelic amyotrophy of the upper limb: MRI findings and the implication on its pathogenesis,” Journal of Clinical Neuromuscular Disease, vol. 13, no. 4, pp. 234–239, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. E. F. Ciceri, L. Chiapparini, A. Erbetta et al., “Angiographically proven cervical venous engorgement: a possible concurrent cause in the pathophysiology of Hirayama's myelopathy,” Neurological Sciences, vol. 31, no. 6, pp. 845–848, 2010. View at Publisher · View at Google Scholar · View at Scopus
  8. K. Boelmans, J. Kaufmann, S. Schmelzer et al., “Hirayama disease is a pure spinal motor neuron disorder—a combined DTI and transcranial magnetic stimulation study,” Journal of Neurology, vol. 260, no. 2, pp. 540–548, 2013. View at Publisher · View at Google Scholar · View at Scopus
  9. C. Cerami, F. Valentino, F. Piccoli, and V. La Bella, “A cervical myelopathy with a Hirayama disease-like phenotype,” Neurological Sciences, vol. 29, no. 6, pp. 451–454, 2008. View at Publisher · View at Google Scholar · View at Scopus
  10. K. Tashiro, S. Kikuchi, Y. Itoyama et al., “Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan,” Amyotrophic Lateral Sclerosis, vol. 7, no. 1, pp. 38–45, 2006. View at Publisher · View at Google Scholar · View at Scopus
  11. C. J. Chen, C. M. Chen, C. L. Wu, L. S. Ro, S. T. Chen, and T. H. Lee, “Hirayama disease: MR diagnosis,” American Journal of Neuroradiology, vol. 19, no. 2, pp. 365–368, 1998. View at Google Scholar
  12. Y. Baba, M. Nakajima, H. Utsunomiya et al., “Magnetic resonance imaging of thoracic epidural venous dilation in Hirayama disease,” Neurology, vol. 62, no. 8, pp. 1426–1428, 2004. View at Publisher · View at Google Scholar · View at Scopus
  13. V. Lai, Y. C. Wong, W. L. Poon, M. K. Yuen, Y. P. Fu, and O. W. Wong, “Forward shifting of posterior dural sac during flexion cervical magnetic resonance imaging in Hirayama disease: an initial study on normal subjects compared to patients with Hirayama disease,” European Journal of Radiology, vol. 80, no. 3, pp. 724–728, 2011. View at Publisher · View at Google Scholar · View at Scopus
  14. H. Yavuz, “A proposal for the definition of Hirayama disease and monomelic amyotrophy,” Journal of Child Neurology, vol. 27, no. 6, pp. 815–818, 2012. View at Google Scholar
  15. U. K. Misra and J. Kalita, “Central motor conduction in Hirayama disease,” Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control, vol. 97, no. 2, pp. 73–76, 1995. View at Publisher · View at Google Scholar · View at Scopus