Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review-Reference-Cited by-同舟云学术

Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review

Published:2017-11-06 Issue:3 Volume:38 Page:268-280
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Miki Tomoko¹²³,Yokota Osamu¹²³^ORCID,Takenoshita Shintaro¹,Mori Yoko⁴,Yamazaki Kiyohiro⁴,Ozaki Yuki⁴,Ueno Shu-ichi⁴,Haraguchi Takashi⁵,Ishizu Hideki³⁶,Kuroda Shigetoshi³⁶,Terada Seishi¹,Yamada Norihito¹

Affiliation:

1. Department of Neuropsychiatry; Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences; Okayama Japan

2. Department of Psychiatry; Kinoko Espoir Hospital; Okayama Japan

3. Department of Psychiatry; Zikei Hospital; Okayama Japan

4. Department of Neuropsychiatry; Ehime University Graduate School of Medicine; Ehime Japan

5. Department of Neurology; National Hospital Organization Minami-Okayama Medical Center; Okayama Japan

6. Department of Laboratory Medicine and Pathology; Zikei Institute of Psychiatry; Okayama Japan

Funder

Grants-in-Aid for Scientific Research (C)

Japanese Ministry of Education, Culture, Sports, Science and Technology

Research Committee of CNS Degenerative Diseases and Research on Dementia

Ministry of Health, Labour and Welfare of Japan

National Center of Neurology and Psychiatry (NCNP)

Zikei Institute of Psychiatry

Strategic Research Program for Brain Sciences from Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12441/fullpdf

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5. Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism;Williams;Brain,2005

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