Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations-Reference-Cited by-同舟云学术

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Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

Published:2007-10-03 Issue:7 Volume:70 Page:521-527
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Chen-Plotkin A. S.,Yuan W.,Anderson C.,Wood E. M.,Hurtig H. I.,Clark C. M.,Miller B. L.,Lee V. M.-Y.,Trojanowski J. Q.,Grossman M.,Deerlin V. M. V.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 53 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. LRRK2: Genetic mechanisms vs genetic subtypes;Handbook of Clinical Neurology;2023

2. Use of transcranial magnetic stimulation in the treatment of nonfluent primary progressive aphasia: a case report;Dementia & Neuropsychologia;2023

3. A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes;Genes;2022-12-14

4. Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review;Cells;2021-01-15

5. Atypical parkinsonism, parkinsonism-plus syndromes and secondary parkinsonian disorders;Principles and Practice of Movement Disorders;2021

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