Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p-Reference-Cited by-同舟云学术

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

Published:2012-02-17 Issue:3 Volume:135 Page:709-722
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Hsiung G.-Y. R.,DeJesus-Hernandez M.,Feldman H. H.,Sengdy P.,Bouchard-Kerr P.,Dwosh E.,Butler R.,Leung B.,Fok A.,Rutherford N. J.,Baker M.,Rademakers R.,Mackenzie I. R. A.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/135/3/709/17347108/awr354.pdf

Reference36 articles.

1. Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies

2. Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

3. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis

4. Motor Neuron dysfunction in frontotemporal dementia

5. TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions

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