Novel Presenilin 1 Mutations Associated With Early Onset of Dementia in a Family With Both Early-Onset and Late-Onset Alzheimer Disease-Reference-Cited by-同舟云学术

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Novel Presenilin 1 Mutations Associated With Early Onset of Dementia in a Family With Both Early-Onset and Late-Onset Alzheimer Disease

Published:2000-10-01 Issue:10 Volume:57 Page:
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Devi Gayatria,Fotiou Alexandra,Jyrinji Darlene,Tycko Benjamin,DeArmand Steve,Rogaeva Ekaterina,Song You-Quiang,Medieros Helena,Liang Yan,Orlacchio Antonio,Williamson Jennifer,St George-Hyslop Peter,Mayeux Richard

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 36 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 presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestations;Alzheimer's & Dementia;2024-06-02

2. Dementia and cognitive decline;Neurogenetics for the Practitioner;2024

3. The presenilin 1 mutation P436S causes familial Alzheimer’s disease with elevated Aβ43 and atypical clinical manifestations;2023-12-06

4. Unraveling Molecular and Genetic Insights into Neurodegenerative Diseases: Advances in Understanding Alzheimer’s, Parkinson’s, and Huntington’s Diseases and Amyotrophic Lateral Sclerosis;International Journal of Molecular Sciences;2023-06-28

5. A Novel PSEN1 Variant Leading to Posterior Cortical Atrophy: A Case Report;Journal of Alzheimer's Disease Reports;2023-05-31

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