Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

Eileen H Bigio*, Jane Wu, Han-Xiang Deng, Esther N. Bit-Ivan, Qinwen Mao, Rakhee Ganti, Melanie Peterson, Nailah Siddique, Changiz Geula, Teepu Siddique, Marek-Marsel Mesulam

*Corresponding author for this work

Research output: Contribution to journalLetter

59 Scopus citations
Original languageEnglish (US)
Pages (from-to)463-465
Number of pages3
JournalActa Neuropathologica
Volume125
Issue number3
DOIs
StatePublished - Mar 1 2013

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

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