FTD-PSP is an Unusual Clinical Phenotype in A Frontotemporal Dementia Patient with A Novel Progranulin Mutation-Reference-Cited by-同舟云学术

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FTD-PSP is an Unusual Clinical Phenotype in A Frontotemporal Dementia Patient with A Novel Progranulin Mutation

Published:2021 Issue:7 Volume:12 Page:1741
ISSN:2152-5250
Container-title:Aging and disease
language:en
Short-container-title:Aging and disease

Author:

Deng Bin,Zheng Zhe,Zheng Jialing,Yang Wanlin,Huang Yu,Luo Yuqi,Jin Dana,Shen Lu,Jin Kunlin,Wang Qing

Publisher

Aging and Disease

Subject

Cell Biology,Neurology (clinical),Geriatrics and Gerontology,Pathology and Forensic Medicine

Reference95 articles.

1. Chang KH, Lee GC, Huang CC, Kuo HC, Chen CM, Hsiao YC, et al. (2018). Genetic and functional characters of GRN p.T487I mutation in Taiwanese patients with atypical parkinsonian disorders. Parkinsonism Relat Disord, 51:61-66.

2. Chitramuthu B, Bennett H, Bateman A (2017). Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease. Brain : a journal of neurology, 140:3081-3104.

3. Finch N, Baker M, Crook R, Swanson K, Kuntz K, Surtees R, et al. (2009). Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain, 132:583-591.

4. Agarwal S, Ahmed RM, D’Mello M, Foxe D, Kaizik C, Kiernan MC, et al. (2019). Predictors of survival and progression in behavioural variant frontotemporal dementia. Eur J Neurol, 26:774-779.

5. Chaplot K, Jarvela TS, Lindberg I (2020). Secreted Chaperones in Neurodegeneration. Front Aging Neurosci, 12:268.

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