Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

Frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) are types of major TDP-43 (43-kDa TAR DNA-binding protein) proteinopathy. Cortical TDP-43 pathology has been analyzed in detail in cases of FTLD-TDP, but is still unclear in cases of ALS. We attempted to clarify the cor...

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Bibliographic Details
Main Authors: Takeuchi, Ryoko, Tada, Mari, Shiga, Atsushi, Toyoshima, Yasuko, Konno, Takuya, Sato, Tomoe, Nozaki, Hiroaki, Kato, Taisuke, Horie, Masao, Shimizu, Hiroshi, Takebayashi, Hirohide, Onodera, Osamu, Nishizawa, Masatoyo, Kakita, Akiyoshi, Takahashi, Hitoshi
Format: Online
Language:English
Published: BioMed Central 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918136/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918136/

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