Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion inC9ORF72: clinicopathologic correlation-Reference-Cited by-同舟云学术

Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion inC9ORF72: clinicopathologic correlation

Published:2012-06-18 Issue:2 Volume:33 Page:122-133
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:

Author:

Bigio Eileen H.,Weintraub Sandra,Rademakers Rosa,Baker Matt,Ahmadian Saman S.,Rademaker Alfred,Weitner Bing Bing,Mao Qinwen,Lee Kyung-Hwa,Mishra Manjari,Ganti Rakhee A.,Mesulam M-Marsel

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1789.2012.01332.x/fullpdf

Reference29 articles.

1. Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011

2. A nexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;Renton;Neuron,2011

3. A Cporf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study;Gijselinck;Lancet Neurol,2012

4. Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72;Murray;Acta Neuropathol,2011

5. p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72 linked FTLD and MND/ALS;Al-Sarraj;Acta Neuropathol,2011

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