Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation

A. Romagnolo, S. Masera, A. Mattioda, G. Superti, F. M. Santorelli, T. Mongini, L. Pinessi, P. Cavalla

Research output: Contribution to journalArticle

Original languageEnglish
JournalEuropean Journal of Neurology
Volume21
Issue number2
DOIs
Publication statusPublished - Feb 2014

Keywords

  • Corpus callosum
  • Hereditary spastic paraplegia
  • Magnetic resonance imaging
  • Multiple sclerosis
  • White matter abnormalities

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Romagnolo, A., Masera, S., Mattioda, A., Superti, G., Santorelli, F. M., Mongini, T., ... Cavalla, P. (2014). Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation. European Journal of Neurology, 21(2). https://doi.org/10.1111/ene.12297

Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation. / Romagnolo, A.; Masera, S.; Mattioda, A.; Superti, G.; Santorelli, F. M.; Mongini, T.; Pinessi, L.; Cavalla, P.

In: European Journal of Neurology, Vol. 21, No. 2, 02.2014.

Research output: Contribution to journalArticle

Romagnolo, A, Masera, S, Mattioda, A, Superti, G, Santorelli, FM, Mongini, T, Pinessi, L & Cavalla, P 2014, 'Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation', European Journal of Neurology, vol. 21, no. 2. https://doi.org/10.1111/ene.12297
Romagnolo, A. ; Masera, S. ; Mattioda, A. ; Superti, G. ; Santorelli, F. M. ; Mongini, T. ; Pinessi, L. ; Cavalla, P. / Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation. In: European Journal of Neurology. 2014 ; Vol. 21, No. 2.
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