A rapidly progressive dementia case with pathological diagnosis of FTLD-UPS

Acta Neuropathol. 2016 Aug;132(2):309-311. doi: 10.1007/s00401-016-1584-7. Epub 2016 Jun 6.

Authors

Abeer Z Tabbarah¹, W Robert Bell¹, Mingkuan Sun¹, Elise Gelwan¹, Olga Pletnikova¹, Argye E Hillis², Juan C Troncoso^{1

2}, Ming-Tseh Lin³, Liam Chen⁴

Affiliations

¹ Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
² Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
³ Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA. mlin36@jhmi.edu.
⁴ Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA. lchen99@jhmi.edu.

PMID: 27271575
DOI: 10.1007/s00401-016-1584-7

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Aged, 80 and over
DNA-Binding Proteins / metabolism
Disease Progression
Endosomal Sorting Complexes Required for Transport / genetics
Female
Frontotemporal Lobar Degeneration / complications*
Frontotemporal Lobar Degeneration / genetics
Frontotemporal Lobar Degeneration / pathology*
Humans
RNA-Binding Protein FUS / metabolism

Substances

CHMP2B protein, human
DNA-Binding Proteins
Endosomal Sorting Complexes Required for Transport
FUS protein, human
RNA-Binding Protein FUS
TARDBP protein, human