LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic-Reference-Cited by-同舟云学术

LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic

Published:2018-07-10 Issue:5 Volume:138 Page:425-431
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neurol Scand

Author:

Ben Romdhan Sawssan¹²³^ORCID,Farhat Nouha¹,Nasri Amina⁴,Lesage Suzanne²,Hdiji Olfa¹,Ben Djebara Mouna⁴,Landoulsi Zied⁴,Stevanin Giovanni²³,Brice Alexis²,Damak Mariem¹,Gouider Riadh⁴,Mhiri Chokri¹

Affiliation:

1. Laboratory of Neurogenetics; Parkinson's Disease and Cerebrovascular Disease; University Hospital Habib Bourguiba; Sfax Tunisia

2. Institut du Cerveau et de la Moelle épinière; INSERM U1127; Sorbonne Université; UPMC Paris VI Univ. UMR_S1127; CNRS UMR 7225; Paris France

3. École Pratique des Hautes Études EPHE; PSL Research University; Paris France

4. Department of Neurology; University Hospital Razi; Tunis; Mannouba Tunisia

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ane.12996/fullpdf

Reference37 articles.

1. Parkinson disease;Poewe;Nat Rev Dis Primers,2017

2. Clinical Features of LRRK2 Carriers with Parkinson’s Disease

3. LRRK2 G2019S in the North African population: a review;Benamer;Eur Neurol,2010

4. Genetic movement disorders in patients of Jewish ancestry;Inzelberg;JAMA Neurol,2014

5. MDS clinical diagnostic criteria for Parkinson's disease;Postuma;Mov Disord,2015

Cited by 23 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. Genetic analysis and natural history of Parkinson’s disease due to the LRRK2 G2019S variant;Brain;2024-05-28

3. Comprehensive analysis of clinical and biological features in Parkinson's disease associated with the LRRK2 G2019S mutation: Data from the PPMI study;Clinical and Translational Science;2024-01

4. Parkinson’s Disease;Movement Disorders Phenomenology;2024

5. Genetic Analysis and Natural History of Parkinson’s Disease Due to the LRRK2 G2019S Variant;2023-10-26