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Distinct spatial contributions of amyloid pathology and cerebral small vessel disease to hippocampal morphology
Alzheimer's & Dementia ( IF 14.0 ) Pub Date : 2024-04-04 , DOI: 10.1002/alz.13791
Kristiana Xhima 1 , Julie Ottoy 1 , Erin Gibson 1 , Katherine Zukotynski 1, 2, 3 , Christopher Scott 1 , Ginelle J. Feliciano 1 , Sabrina Adamo 1 , Phillip H. Kuo 4 , Michael J. Borrie 5 , Howard Chertkow 6 , Richard Frayne 7 , Robert Laforce 8 , Michael D. Noseworthy 2, 9 , Frank S. Prato 5 , Demetrios J. Sahlas 10 , Eric E. Smith 11 , Vesna Sossi 12 , Alexander Thiel 13 , Jean‐Paul Soucy 14 , Jean‐Claude Tardif 15 , Maged Goubran 1, 16, 17 , Sandra E. Black 1, 18 , Joel Ramirez 1 ,
Affiliation  

Cerebral small vessel disease (SVD) and amyloid beta (Aβ) pathology frequently co-exist. The impact of concurrent pathology on the pattern of hippocampal atrophy, a key substrate of memory impacted early and extensively in dementia, remains poorly understood.

中文翻译:

淀粉样蛋白病理学和脑小血管疾病对海马形态的独特空间贡献

脑小血管病(SVD)和β淀粉样蛋白(Aβ)病理经常同时存在。并发病理学对海马萎缩模式的影响仍然知之甚少,海马萎缩是痴呆症早期和广泛影响的记忆的关键基础。
更新日期:2024-04-07
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