An autopsy case of corticobasal syndrome due to asymmetric degeneration of the motor cortex and substantia nigra with TDP ‐43 proteinopathy, associated with Alzheimer's disease pathology-Reference-Cited by-同舟云学术

An autopsy case of corticobasal syndrome due to asymmetric degeneration of the motor cortex and substantia nigra with TDP ‐43 proteinopathy, associated with Alzheimer's disease pathology

Published:2021-02-03 Issue:3 Volume:41 Page:214-225
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Tando So¹,Kasai Takashi²,Mizuta Ikuko²,Takahashi Hisashi¹²,Yaoi Takeshi¹,Saito Kozo²,Hojo Tomohito³,Mizuno Toshiki²,Hasegawa Masato⁴^ORCID,Itoh Kyoko¹^ORCID

Affiliation:

1. Department of Pathology and Applied Neurobiology Kyoto Prefectural University of Medicine Kyoto Japan

2. Department of Neurology Kyoto Prefectural University of Medicine Kyoto Japan

3. Department of Surgical Pathology Kyoto Prefectural University of Medicine Kyoto Japan

4. Dementia Research Project Tokyo Metropolitan Institute of Medical Science Tokyo Japan

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/neup.12723

Reference29 articles.

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

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

3. Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies

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

5. Accumulation of phosphorylated TDP-43 in brains of patients with argyrophilic grain disease

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