A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations-Reference-Cited by-同舟云学术

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A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations

Published:2009-05 Issue:4 Volume:15 Page:273-276
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Lohmann Ebba,Leclere Laurence,De Anna Francesca,Lesage Suzanne,Dubois Bruno,Agid Yves,Dürr Alexandra,Brice Alexis

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference13 articles.

1. Update on the genetics of Parkinson's disease;Gasser;Movement Disorders,2007

2. Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data;Khan;Brain,2005

3. Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia;Saunders-Pullman;Neuroscience Letters,2006

4. Idiopathic hyposmia as a preclinical sign of Parkinson's disease;Ponsen;Annals of Neurology,2004

5. Olfactory loss may be a first sign of idiopathic Parkinson's disease;Haehner;Movement Disorders,2007

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

2. Olfactory Dysfunction in Parkinson’s Disease and Related Disorders;Non-Motor Parkinson's Disease;2022-03-10

3. Profiling Non-motor Symptoms in Monogenic Parkinson’s Disease;Frontiers in Aging Neuroscience;2020-10-30

4. Olfactory Dysfunction in Familial and Sporadic Parkinson's Disease;Frontiers in Neurology;2020-05-29

5. Cognitive and psychiatric symptoms in genetically determined Parkinson’s disease: a systematic review;European Journal of Neurology;2019-11-28

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