Frontotemporal dementia with parkinsonism linked to chromosome 17 with theMAPT R406W mutation presenting with a broad distribution of abundant senile plaques-Reference-Cited by-同舟云学术

Frontotemporal dementia with parkinsonism linked to chromosome 17 with theMAPT R406W mutation presenting with a broad distribution of abundant senile plaques

Published:2014-11-06 Issue:1 Volume:35 Page:75-82
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Ishida Chiho¹,Kobayashi Katsuji²,Kitamura Tatsuru³,Ujike Hiroshi⁴,Iwasa Kazuo⁵,Yamada Masahito⁵

Affiliation:

1. Department of Neurology; National Hospital Organization Iou Hospital; Komatsu Japan

2. Department of Psychiatry; Awazu Neuropsychiatric Sanatorium; Komatsu Japan

3. Department of Psychiatry; Ishikawa Prefectual Takamatsu Hospital; Kahoku Japan

4. Ujike Nishiguchi Clinic; Okayama Japan

5. Department of Neurology; Neurobiology of Aging; Kanazawa University Graduate School of Medical Science; Kanazawa Japan

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12154/fullpdf

Reference20 articles.

1. Autosomal dominant dementia with widespread neurofibrillary tangles;Reed;Ann Neurol,1997

2. Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation;Lindquist;Eur J Neurol,2008

3. Phenotypic variation in hereditary frontotemporal dementia with tau mutations;Swieten;Ann Neurol,1999

4. Coexistent tau and amyloid pathology in hereditary frontotemporal dementia with tau mutations;Rosso;Ann N Y Acad Sci,2000

5. Imaging findings of familial dementia with a tau R406W mutation;Komatsu;Acta Neurol Belg,2011

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