Neuropathological features of Japanese familial amyotrophic lateral sclerosis with p.N352S mutation inTARDBP-Reference-Cited by-同舟云学术

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Neuropathological features of Japanese familial amyotrophic lateral sclerosis with p.N352S mutation inTARDBP

Published:2014-01-21 Issue:2 Volume:40 Page:231-236
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Homma T.¹²,Nagaoka U.³,Kawata A.³,Mochizuki Y.¹⁴,Kawakami H.⁵,Maruyama H.⁵,Matsubara S.³,Komori T.¹

Affiliation:

1. Department of Laboratory Medicine and Pathology (Neuropathology); Tokyo Metropolitan Neurological Hospital; Tokyo Japan

2. Department of Pathology; Saitama Medical University; Saitama Japan

3. Department of Neurology; Tokyo Metropolitan Neurological Hospital; Tokyo Japan

4. Department of Neurology; Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled; Tokyo Japan

5. Department of Epidemiology, Research Institute for Radiation Biology and Medicine; Hiroshima University; Hiroshima Japan

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Reference12 articles.

1. Screening for TARDBP mutations in Japanease familial amyotrophic lateral sclerosis;Kamada;J Neurol Sci,2009

2. An improved protocol for the analysis of SOD1 gene mutations and a new mutation in exon 4;Yulug;Hum Mol Genet,1995

3. Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistory;Braak;Acta Neuropathol,2006

4. Neuropathological staging of Alzheimer-related changes;Braak;Acta Neuropathol,1991

5. Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations;Kühnlein;Arch Neurol,2008

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1. Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant;Neuropathology and Applied Neurobiology;2024-02

2. Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia–Amyotrophic Lateral Sclerosis Patients;Brain Sciences;2021-09-19

3. p.N345K mutation in TARDBP in a patient with familial amyotrophic lateral sclerosis: An autopsy case;Neuropathology;2019-05-24

4. ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation;Acta Neuropathologica Communications;2015-10-09

5. An autopsy case of familial amyotrophic lateral sclerosis with aTARDBPQ343R mutation;Neuropathology;2015-06-12

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