Phenotypic variability and its pathological basis in amyotrophic lateral sclerosis
Author:
Affiliation:
1. Department of NeurologyNational Hospital Organization Chibahigashi National Hospital Chiba Japan
2. Department of NeurologyTokyo Women's Medical University Tokyo Japan
Publisher
Wiley
Subject
Clinical Neurology,General Medicine,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/neup.12606
Reference121 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. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis
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