Skip to main content
Log in

An autopsy confirmed case of progressive supranuclear palsy with predominant cerebellar ataxia

  • Letter to the Editors
  • Published:
Journal of Neurology Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

References

  1. Williams DR, Lees AJ (2009) Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges. Lancet Neurol 8:270–279

    Article  PubMed  Google Scholar 

  2. Kanazawa M, Shimohata T, Toyoshima Y et al (2009) Cerebellar involvement in progressive supranuclear palsy: a clinicopathological study. Mov Disord 24:1312–1318

    Article  PubMed  Google Scholar 

  3. Litvan I, Agid Y, Calne D et al (1996) Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology 47:1–9

    Article  CAS  PubMed  Google Scholar 

  4. Kanazawa M, Tada M, Onodera O et al (2013) Early clinical features of patients with progressive supranuclear palsy with predominant cerebellar ataxia Parkinsonism and related disoders. Parkinsonism Relat Disord 19:1149–1151

    Article  PubMed  Google Scholar 

  5. Jellinger K (2010) Cerebellar involvement in progressive supranuclear palsy. Mov Disord 25:1104–1105

    Article  PubMed  Google Scholar 

  6. Kouri N, Oshima K, Takahashi M et al (2013) Corticobasal degeneration with olivopontocerebellar atrophy and TDP-43 pathology: an unusual clinicopathologic variant of CBD. Acta Neuropathol 125:741–752

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Cordato NJ, Halliday M, Harding AJ et al (2000) Regional brain atrophy in progressive supranuclear palsy and Lewy body disease. Ann Neurol 47:718–728

    Article  CAS  PubMed  Google Scholar 

  8. Schofield EC, Hodges JR, Macdonald V et al (2010) Cortical atrophy differentiates Richardson’s syndrome from the parkinsonian form of progressive supranuclear palsy. Mov Disord 26:256–263

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

This study was supported by the Original Technology Research Program for Brain Science through the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP) (No. 2014M3C7A1064752), and clinical research grant from Pusan National University Hospital 2015. We thank our patient and his family for donating brain to the Pusan National University Hospital Brain Bank to contribute to dementia research.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Gi Yeong Huh or Eun-Joo Kim.

Ethics declarations

Financial disclosure

None reported.

Conflicts of interest

On behalf of all authors, the corresponding author states that there is no conflict of interest.

Ethical standard

The study has been approved by the institutional review boards and has, therefore, been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki.

Additional information

Gi Yeong Huh, Eun-Joo Kim contribute equally.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 1613 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lee, M.J., Lee, J.H., Kim, BK. et al. An autopsy confirmed case of progressive supranuclear palsy with predominant cerebellar ataxia. J Neurol 263, 2540–2543 (2016). https://doi.org/10.1007/s00415-016-8303-0

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00415-016-8303-0

Keywords

Navigation