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 Y. Wu, Han Xiang Deng, Esther N. Bit-Ivan, Qinwen Mao, Rakhee Ganti, Melanie Peterson, Nailah Siddique, Changiz Geula, Teepu Siddique, Marsel Mesulam

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

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

ASJC Scopus subject areas

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

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