早发性阿尔茨海默病伴罕见PSEN1（Arg278Gly）突变患者的淀粉样蛋白和tau蛋白PET检查结果呈阳性 - Suppr

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超能文献

Positive amyloid and tau PET in an early-onset Alzheimer's disease with a rare PSEN1 (Arg278Gly) mutation.

作者信息

Yang Liu, Dong Ping, Li Li, Li Lin, Su Minggang

机构信息

Department of Nuclear Medicine, West China Hospital, Sichuan University, Guoxue Alley 37#, Chengdu, 610041, P.R. China.

出版信息

Eur J Nucl Med Mol Imaging. 2025 Feb;52(3):1225-1227. doi: 10.1007/s00259-024-06917-1. Epub 2024 Sep 9.

DOI:10.1007/s00259-024-06917-1

PMID:39249491

Abstract

摘要

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本文引用的文献

Diagnostic performance of molecular imaging methods in predicting the progression from mild cognitive impairment to dementia: an updated systematic review.分子成像方法在预测轻度认知障碍向痴呆进展中的诊断性能：一项更新的系统评价

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A comparison of visual assessment and semi-quantification for the diagnostic and prognostic use of [F]flortaucipir PET in a memory clinic cohort.在记忆门诊队列中，[F]氟替卡匹PET诊断和预后应用的视觉评估与半定量比较。

Eur J Nucl Med Mol Imaging. 2024 May;51(6):1639-1650. doi: 10.1007/s00259-023-06583-9. Epub 2024 Jan 6.

Quantification of amyloid PET for future clinical use: a state-of-the-art review.用于未来临床应用的淀粉样 PET 的量化：最新综述。

Eur J Nucl Med Mol Imaging. 2022 Aug;49(10):3508-3528. doi: 10.1007/s00259-022-05784-y. Epub 2022 Apr 7.

Outcomes of clinical utility in amyloid-PET studies: state of art and future perspectives.淀粉样蛋白-PET 研究的临床效用结果：现状与未来展望。

Eur J Nucl Med Mol Imaging. 2021 Jul;48(7):2157-2168. doi: 10.1007/s00259-020-05187-x. Epub 2021 Feb 17.

A Rare PSEN1 (Leu85Pro) Mutation Causing Alzheimer's Disease in a 29-Year-Old Woman Presenting as Corticobasal Syndrome.一个罕见的 PSEN1（亮氨酸 85 脯氨酸）突变导致 29 岁女性阿尔茨海默病，表现为皮质基底节综合征。

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