Japanese Familial Cases of Frontotemporal Dementia and Parkinsonism with N279K Tau Gene Mutation-Reference-Cited by-同舟云学术

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Japanese Familial Cases of Frontotemporal Dementia and Parkinsonism with N279K Tau Gene Mutation

Published:2020-11-03 Issue:1 Volume:8 Page:126-132
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Oka Yuwa¹^ORCID,Saiki Hidemoto¹,Hashimoto Yasumasa¹²,Terada Yuta¹³,Nakamura Takashi¹⁴,Ayaki Takashi³,Orimo Satoshi⁵,Matsumoto Sadayuki¹

Affiliation:

1. Department of Neurology Kitano Hospital, Tazuke Kofukai Medical Research Institute Osaka Japan

2. Department of Molecular Therapy National Center of Neurology and Psychiatry, National Institute of Neuroscience Kodaira Japan

3. Department of Neurology Kyoto University Graduate School of Medicine Kyoto Japan

4. Department of Neurology Osaka Saiseikai Nakatsu Hospital Osaka Japan

5. Department of Neurology Kanto Central Hospital of the Mutual Aid Association of Public‐School Teachers Tokyo Japan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13100

Reference15 articles.

1. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies

2. Parkinsonian syndrome in familial frontotemporal dementia

3. Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)

4. Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17

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

Cited by 3 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. A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy;Frontiers in Neurology;2024-04-19

2. Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of MAPT Mutations: A Systematic Review;Frontiers in Bioscience-Landmark;2024-01-16

3. Parkinsonism and dementia;Journal of the Neurological Sciences;2022-02

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