Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features-Reference-Cited by-同舟云学术

Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features

Published:2019-02-17 Issue:4 Volume:34 Page:568-574
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Ikeda Aya¹,Shimada Hitoshi²,Nishioka Kenya¹,Takanashi Masashi¹,Hayashida Arisa¹,Li Yuanzhe¹,Yoshino Hiroyo³,Funayama Manabu¹³,Ueno Yuji¹,Hatano Taku¹,Sahara Naruhiko²,Suhara Tetsuya²,Higuchi Makoto²,Hattori Nobutaka¹³

Affiliation:

1. Department of NeurologyJuntendo University School of Medicine Tokyo Japan

2. Department of Functional Brain Imaging ResearchNational Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology Chiba Japan

3. Research Institute for Diseases of Old Age, Graduate School of MedicineJuntendo University Tokyo Japan

Funder

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27623

Reference37 articles.

1. Tau pathology and neurodegeneration