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July 11, 2006; 67 (1) Articles

Clinical features of hereditary spastic paraplegia due to spastin mutation

C. J. McDermott, C. E. Burness, J. Kirby, L. E. Cox, D. G. Rao, C. Hewamadduma, B. Sharrack, M. Hadjivassiliou, P. F. Chinnery, A. Dalton, P. J. Shaw
First published July 10, 2006, DOI: https://doi.org/10.1212/01.wnl.0000223315.62404.00
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Article Information

vol. 67 no. 1 45-51
DOI: 
https://doi.org/10.1212/01.wnl.0000223315.62404.00
PubMed: 
16832076
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published July 10, 2006.
Copyright & Usage: 
© 2006

Author Disclosures

    1. C. J. McDermott, PhD,
    2. C. E. Burness, MSc,
    3. J. Kirby, PhD,
    4. L. E. Cox, BSc,
    5. D. G. Rao, MD,
    6. C. Hewamadduma, MBBS,
    7. B. Sharrack, PhD,
    8. M. Hadjivassiliou, MD,
    9. P. F. Chinnery, PhD,
    10. A. Dalton, PhD,
    11. P. J. Shaw, MD and
    12. on behalf of the UK and Irish HSP Consortium*
  1. C. J. McDermott, PhD,
  2. C. E. Burness, MSc,
  3. J. Kirby, PhD,
  4. L. E. Cox, BSc,
  5. D. G. Rao, MD,
  6. C. Hewamadduma, MBBS,
  7. B. Sharrack, PhD,
  8. M. Hadjivassiliou, MD,
  9. P. F. Chinnery, PhD,
  10. A. Dalton, PhD,
  11. P. J. Shaw, MD and
  12. on behalf of the UK and Irish HSP Consortium*
  1. From the Sheffield Care and Research Centre for Motor Neuron Disorders, Academic Neurology Unit, University of Sheffield, Sheffield, UK (C.J.M., C.E.B., J.K., L.E.C., D.G.R., C.H., B.S., M.H., P.J.S.); Sheffield Molecular Genetics Service, Sheffield Children’s NHS Trust, Sheffield, UK (A.D.); and Department of Neurology, University of Newcastle upon Tyne, Newcastle upon Tyne, UK (P.F.C.).
  1. Address correspondence and reprint requests to Dr Shaw, Academic Neurology Unit, Sheffield University, Sheffield, UK; e-mail: pamela.shaw{at}sheffield.ac.uk
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