Amyotrophic Lateral Sclerosis with Pallidonigroluysian Degeneration: A Clinicopathological Study-Reference-Cited by-同舟云学术

Amyotrophic Lateral Sclerosis with Pallidonigroluysian Degeneration: A Clinicopathological Study

Published:2019-12-10 Issue:2 Volume:87 Page:302-312
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Ito Junko¹^ORCID,Shimizu Hiroshi¹,Ohta Kentaro²,Idezuka Jiro³,Tanaka Hajime⁴,Kondo Hiroshi⁵,Nakajima Takashi²,Takahashi Hitoshi¹,Akazawa Kohei⁶,Onodera Osamu⁷,Kakita Akiyoshi¹

Affiliation:

1. Department of PathologyBrain Research Institute, Niigata University Niigata

2. Department of NeurologyNational Hospital Organization Niigata National Hospital Kashiwazaki

3. Department of NeurologyOjiya Sakura Hospital Ojiya

4. Department of NeurologyShinrakuen Hospital Niigata

5. Department of Neurology, Brain Disease CenterAgano Hospital Agano

6. Department of Medical InformaticsNiigata University Medical and Dental Hospital Niigata

7. Department of NeurologyBrain Research Institute, Niigata University Niigata Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25652

Reference32 articles.

1. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

2. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

3. Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions

4. Evidence of Multisystem Disorder in Whole-Brain Map of Pathological TDP-43 in Amyotrophic Lateral Sclerosis

5. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis

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