Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study

Published:2014-12-09 Issue:2 Volume:30 Page:253-258
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Nabli Fatma¹,Ben Sassi Samia¹,Amouri Rim¹,Duda John E.²,Farrer Matthew J.³,Hentati Fayçal¹

Affiliation:

1. Neurology Department; National Institute Mongi Ben Hmida of Neurology, Faculty of Medicine of Tunis, University Tunis El Manar; Tunis Tunisia

2. Parkinson's Disease Research; Education and Clinical Center, Philadelphia VA Medical Center; Philadelphia PA USA

3. Djavad Mowafhaghian Centre for Brain Health, University of British Columbia; Vancouver Canada

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference23 articles.

1. LRRK2 and Parkinson disease;Dachsel;Arch Neurol,2010

2. Autosomal dominant Parkinson's disease;Sundal;Parkinsonism Relat Disord,2012

3. The genetics of Parkinson disease;Bekris;Geriatr Psychiatry Neurol,2010

4. Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review;Guedes;Parkinsonism Relat Disord,2009

5. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans;Lesage;Hum Mol Genet,2010

Cited by 29 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. The Impact of LRRK2 G2019S on Parkinson’s Disease: Clinical Phenotype and Treatment in Tunisian Patients;Journal of Movement Disorders;2024-07-31

2. Prediction of Parkinson’s disease pathogenic variants using hybrid Machine learning systems and radiomic features;Physica Medica;2023-09

3. Comparing the effects of GBA variants and onset age on clinical features and progression in Parkinson's disease;CNS Neuroscience & Therapeutics;2023-08-10

4. LRRK2: Genetic mechanisms vs genetic subtypes;Handbook of Clinical Neurology;2023

5. Molecular mechanisms defining penetrance of LRRK2-associated Parkinson’s disease;Medizinische Genetik;2022-06-01

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