An autopsy case of familial amyotrophic lateral sclerosis with aTARDBPQ343R mutation

Author:

Okamoto Koichi1,Fujita Yukio2,Hoshino Eri2,Tamura Yuhji3,Fukuda Toshio4,Hasegawa Masato5,Takatama Masamitsu6

Affiliation:

1. Department of Neurology; Geriatrics Research Institute and Hospital; Maebashi Japan

2. Department of Neurology; Gunma University Graduate School of Medicine; Maebashi Japan

3. Department of Internal Medicine; Kiboukan Hospital; Takasaki Japan

4. Department of Histopathology and Cytopathology; Gunma University Graduate School of Health Sciences; Maebashi Japan

5. Department of Neuropathology and Cell Biology; Tokyo Metropolitan Institute of Medical Science; Tokyo Japan

6. Department of Internal Medicine; Geriatrics Research Institute and Hospital; Maebashi Japan

Publisher

Wiley

Subject

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

Reference32 articles.

1. Amyotrophic lateral sclerosis;Wijesekera;Orphanet J Rare Dis,2009

2. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Arai;Biochem Biophys Res Commun,2006

3. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Neumann;Science,2006

4. Ubiquitin-positive tau-negative intraneuronal inclusions in dementia with motor neuron disease;Okamoto;Neuropathology,2010

5. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Hasegawa;Ann Neurol,2008

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