Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation

Rossana Terlizzi, Maria Lucia Valentino, Anna Bartoletti-Stella, Marta Columbaro, Silvia Piras, Michelangelo Stanzani-Maserati, Marialuisa Quadri, Guido J. Breedveld, Vincenzo Bonifati, Paolo Martinelli, Piero Parchi, Sabina Capellari

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)1-2
Number of pages2
JournalMovement Disorders
Issue number8
Publication statusAccepted/In press - 2017


  • Ceroid lipofuscinosis inclusions
  • Corticobasal syndrome
  • Frontotemporal lobar degeneration
  • Granulin gene
  • Lysosomal storage

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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