日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Structural and functional brain abnormalities place phenocopy frontotemporal dementia (FTD) in the FTD spectrum

结构和功能性脑异常将表型模拟额颞叶痴呆(FTD)归入FTD谱系。

Steketee, Rebecca M E; Meijboom, Rozanna; Bron, Esther E; Osse, Robert Jan; de Koning, Inge; Jiskoot, Lize C; Klein, Stefan; de Jong, Frank Jan; van der Lugt, Aad; van Swieten, John C; Smits, Marion

Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study

MAPT和GRN基因突变携带者无症状期脑血流量:一项纵向动脉自旋标记研究

Dopper, Elise G P; Chalos, Vicky; Ghariq, Eidrees; den Heijer, Tom; Hafkemeijer, Anne; Jiskoot, Lize C; de Koning, Inge; Seelaar, Harro; van Minkelen, Rick; van Osch, Matthias J P; Rombouts, Serge A R B; van Swieten, John C

Cerebral small vessel disease affects white matter microstructure in mild cognitive impairment

脑小血管病影响轻度认知障碍患者的白质微结构

Papma, Janne M; de Groot, Marius; de Koning, Inge; Mattace-Raso, Francesco U; van der Lugt, Aad; Vernooij, Meike W; Niessen, Wiro J; van Swieten, John C; Koudstaal, Peter J; Prins, Niels D; Smits, Marion

The influence of cerebral small vessel disease on default mode network deactivation in mild cognitive impairment

脑小血管病对轻度认知障碍患者默认模式网络失活的影响

Papma, Janne M; den Heijer, Tom; de Koning, Inge; Mattace-Raso, Francesco U; van der Lugt, Aad; van der Lijn, Fedde; van Swieten, John C; Koudstaal, Peter J; Smits, Marion; Prins, Niels D

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

由新型 C.314dup 前粒蛋白突变引起的对称性皮质基底节综合征

Dopper Elise G P, Seelaar Harro, Chiu Wang Zheng, de Koning Inge, van Minkelen Rick, Baker Matthew C, Rozemuller Annemieke J M, Rademakers Rosa, van Swieten John C