Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene

Published:2017-02 Issue: Volume:35 Page:82-87
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Bougea Anastasia,Koros Christos,Stamelou Maria,Simitsi Athina,Papagiannakis Nikolaos,Antonelou Roubina,Papadimitriou Dimitra,Breza Marianthi,Tasios Konstantinos,Fragkiadaki Stella,Geronicola Trapali Xenia,Bourbouli Mara,Koutsis Georgios,Papageorgiou Sokratis G.,Kapaki Elisabeth,Paraskevas George P.,Stefanis Leonidas

Funder

MULTISYN European Program

MEFOPA

THALIS

Michael J. Fox Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference13 articles.

1. The many faces of alpha-synuclein mutations;Kasten;Mov. Disord.,2013

2. Motor and nonmotor features of carriers of the p.A53T alpha-synuclein mutation: a longitudinal study;Papadimitriou;Mov. Disord.,2016

3. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia;Rascovsky;Brain,2011

4. A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations;Kara;JAMA Neurol.,2014

5. Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation;Kiely;Mol. Neurodegener.,2015

Cited by 26 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. Defining the Riddle in Order to Solve It: There Is More Than One “Parkinson's Disease”;Movement Disorders;2023-05-08

2. Impact of APOE Genotype on Cognition in Idiopathic and Genetic Forms of Parkinson's Disease;Movement Disorders;2023-05

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

4. Cognitive Impairment in Genetic Parkinson’s Disease;Parkinson's Disease;2021-12-30

5. Genotype-Phenotype Correlations in Monogenic Parkinson Disease: A Review on Clinical and Molecular Findings;Frontiers in Neurology;2021-09-22

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3