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

Active lifestyles moderate clinical outcomes in autosomal dominant frontotemporal degeneration

积极的生活方式可改善常染色体显性遗传性额颞叶变性的临床结果

Casaletto, K B; Staffaroni, A M; Wolf, A; Appleby, B; Brushaber, D; Coppola, G; Dickerson, B; Domoto-Reilly, K; Elahi, F M; Fields, J; Fong, J C; Forsberg, L; Ghoshal, N; Graff-Radford, N; Grossman, M; Heuer, H W; Hsiung, G-Y; Huey, E D; Irwin, D; Kantarci, K; Kaufer, D; Kerwin, D; Knopman, D; Kornak, J; Kramer, J H; Litvan, I; Mackenzie, I R; Mendez, M; Miller, B; Rademakers, R; Ramos, E M; Rascovsky, K; Roberson, E D; Syrjanen, J A; Tartaglia, M C; Weintraub, S; Boeve, B; Boxer, A L; Rosen, H; Yaffe, K

Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohort

北美人群中散发性和家族性行为变异型额颞叶痴呆(FTD)的比较

Heuer, Hilary W; Wang, P; Rascovsky, K; Wolf, A; Appleby, B; Bove, J; Bordelon, Y; Brannelly, P; Brushaber, D E; Caso, C; Coppola, G; Dickerson, B; Dickinson, S; Domoto-Reilly, K; Faber, K; Ferrall, J; Fields, J; Fishman, A; Fong, J; Foroud, T; Forsberg, L K; Gearhart, D; Ghazanfari, B; Ghoshal, N; Goldman, J; Graff-Radford, J; Graff-Radford, N; Grant, I; Grossman, M; Haley, D; Hsiung, G-Y; Huey, E; Irwin, D; Jones, D; Kantarci, K; Karydas, A; Kaufer, D; Kerwin, D; Knopman, D; Kornak, J; Kramer, J H; Kraft, R; Kremers, W K; Kukull, W; Litvan, I; Ljubenkov, P; Mackenzie, I R; Maldonado, M; Manoochehri, M; McGinnis, S; McKinley, E; Mendez, M F; Miller, B L; Onyike, C; Pantelyat, A; Pearlman, R; Petrucelli, L; Potter, M; Rademakers, R; Ramos, E M; Rankin, K P; Roberson, E D; Rogalski, E; Sengdy, P; Shaw, L; Syrjanen, J; Tartaglia, M C; Tatton, N; Taylor, J; Toga, A; Trojanowski, J; Weintraub, S; Wong, B; Wszolek, Z; Boeve, B F; Rosen, H J; Boxer, A L

Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities

白质异常患者集落刺激因子1受体功能部分丧失

Konno, T; Miura, T; Harriott, A M; Mezaki, N; Edwards, E S; Rademakers, R; Ross, O A; Meschia, J F; Ikeuchi, T; Wszolek, Z K

Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy

由微管相关蛋白tau (MAPT) p.P301L突变引起的17号染色体相关额颞叶痴呆和帕金森综合征 (FTDP-17) 存在临床病理异质性,其中包括一例球状胶质tau蛋白病患者。

Tacik, P; Sanchez-Contreras, M; DeTure, M; Murray, M E; Rademakers, R; Ross, O A; Wszolek, Z K; Parisi, J E; Knopman, D S; Petersen, R C; Dickson, D W

Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images

遗传性和散发性额颞叶痴呆患者的脑萎缩随时间推移而发生:一项基于198例连续磁共振成像的研究

Whitwell, J L; Boeve, B F; Weigand, S D; Senjem, M L; Gunter, J L; Baker, M C; DeJesus-Hernandez, M; Knopman, D S; Wszolek, Z K; Petersen, R C; Rademakers, R; Jack, C R Jr; Josephs, K A

Progressive supranuclear palsy in a family with TDP-43 pathology

TDP-43病理家族中的进行性核上性麻痹

Kertesz, A; Finger, E; Murrell, J; Chertkow, H; Ang, L C; Baker, M; Ravenscroft, T; Rademakers, R; Munoz, D G

Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin

携带前粒蛋白基因突变的同卵双胞胎具有相似的临床和神经影像学特征

McDade, E; Boeve, B F; Burrus, T M; Boot, B P; Kantarci, K; Fields, J; Lowe, V J; Peller, P; Knopman, D; Baker, M; Finch, N; Rademakers, R; Petersen, R

Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTD

无症状MAPT患者功能连接改变:与bvFTD的比较

Whitwell, J L; Josephs, K A; Avula, R; Tosakulwong, N; Weigand, S D; Senjem, M L; Vemuri, P; Jones, D T; Gunter, J L; Baker, M; Wszolek, Z K; Knopman, D S; Rademakers, R; Petersen, R C; Boeve, B F; Jack, C R Jr

Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN

FTD 患者脑和海马萎缩的轨迹,伴有 MAPT 或 GRN 基因突变

Whitwell, J L; Weigand, S D; Gunter, J L; Boeve, B F; Rademakers, R; Baker, M; Knopman, D S; Wszolek, Z K; Petersen, R C; Jack, C R Jr; Josephs, K A

Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

在一名非裔美国人散发性肌萎缩侧索硬化症(ALS)患者中发现VCP基因的新型p.Ile151Val突变。

DeJesus-Hernandez, M; Desaro, P; Johnston, A; Ross, O A; Wszolek, Z K; Ertekin-Taner, N; Graff-Radford, N R; Rademakers, R; Boylan, K