Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)-Reference-Cited by-同舟云学术

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Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

Published:2002-12-10 Issue:11 Volume:59 Page:1791-1793
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Tsuboi Y.,Baker M.,Hutton M. L.,Uitti R. J.,Rascol O.,Delisle M.-B.,Soulages X.,Murrell J. R.,Ghetti B.,Yasuda M.,Komure O.,Kuno S.,Arima K.,Sunohara N.,Kobayashi T.,Mizuno Y.,Wszolek Z. K.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genotype-phenotype correlation in the spectrum of frontotemporal dementia-parkinsonian syndromes and advanced diagnostic approaches;Critical Reviews in Clinical Laboratory Sciences;2022-12-12

2. Japanese Familial Cases of Frontotemporal Dementia and Parkinsonism with N279K Tau Gene Mutation;Movement Disorders Clinical Practice;2020-11-03

3. Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features;Movement Disorders;2019-02-17

4. Frontotemporal dementia;Handbook of Clinical Neurology;2019

5. 11C-CFT-PET in Presymptomatic FTDP-17: A Potential Biomarker Predicting Onset;Journal of Alzheimer's Disease;2017-12-19

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