Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem-Reference-Cited by-同舟云学术

Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem

Published:2022-11-04 Issue:1 Volume:82 Page:29-37
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:

Author:

Hamasaki Hideomi,Maeda Norihisa,Sasagasako Naokazu,Honda Hiroyuki,Shijo Masahiro,Mori Shin-Ichiro,Yagita Kaoru,Arahata Hajime,Iwaki Toru

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Link

https://academic.oup.com/jnen/article-pdf/82/1/29/48179830/nlac097.pdf

Reference49 articles.

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2. New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1). The International Myotonic Dystrophy Consortium (IDMC);Neurology,2000

3. Risk prediction for clinical phenotype in myotonic dystrophy type 1: Data from 2,650 patients;Salehi;Genetic Test,2007

4. Hypogonadism in DM1 and its relationship to erectile dysfunction;Antonini;J Neurol,2011

5. Cognitive decline over time in adults with myotonic dystrophy type 1: A 9-year longitudinal study;Gallais;Neuromuscul Disord,2017

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1. Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1);International Journal of Molecular Sciences;2023-01-22