Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease-Reference-Cited by-同舟云学术

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Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease

Published:2012-03 Issue:3 Volume:18 Page:243-246
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Ben Sassi Samia,Nabli Fatma,Hentati Emna,Nahdi Houda,Trabelsi Meriam,Ben Ayed Hela,Amouri Rim,Duda John Eric,Farrer Matthew John,Hentati Fayçal

Funder

Michael J. Fox Foundation

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference12 articles.

1. Molecular pathogenesis of Parkinson’s disease;Eriksen;Arch Neurol,2005

2. LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study;Hulihan;Lancet Neurol,2008

3. International LRRK2 Consortium. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson’s disease: a case-control study;Healy;Lancet Neurol,2008

4. Lrrk2 and Lewy body disease;Ross;Ann Neurol,2006

5. Familial Parkinson’s disease: clinical and genetic analysis of four Basque families;Paisan-Ruiz;Ann Neurol,2005

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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 background of cognitive decline in Parkinson's disease;Frontiers in Cognition;2024-07-22

3. Emerging perspectives on precision therapy for Parkinson’s disease: multidimensional evidence leading to a new breakthrough in personalized medicine;Frontiers in Aging Neuroscience;2024-07-04

4. Influence of cognitive reserve on cognitive and motor function in α-synucleinopathies: A systematic review and multilevel meta-analysis;Neuroscience & Biobehavioral Reviews;2024-06

5. Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores;npj Parkinson's Disease;2024-01-04

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