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

LGI1 antibody encephalitis: acute treatment comparisons and outcome

LGI1抗体脑炎:急性期治疗比较及预后

Rodriguez, Andrew; Klein, C J; Sechi, Elia; Alden, Eva; Basso, Michael R; Pudumjee, Shehroo; Pittock, Sean J; McKeon, Andrew; Britton, Jeffrey W; Lopez-Chiriboga, A Sebastian; Zekeridou, Anastasia; Zalewski, Nicholas L; Boeve, B F; Day, Gregory S; Gadoth, Avi; Burkholder, David; Toledano, Michel; Dubey, Divyanshu; Flanagan, Eoin P

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

[(18)F] AV-1451 uptake in corticobasal syndrome: the influence of beta-amyloid and clinical presentation

[(18)F] AV-1451 在皮质基底节综合征中的摄取:β-淀粉样蛋白和临床表现的影响

Ali, F; Whitwell, J L; Martin, P R; Senjem, M L; Knopman, D S; Jack, C R; Lowe, V J; Petersen, R C; Boeve, B F; Josephs, K A

Multiple sclerosis masquerading as Alzheimer-type dementia: Clinical, radiological and pathological findings

多发性硬化症伪装成阿尔茨海默病型痴呆:临床、放射学和病理学发现

Tobin, W O; Popescu, B F; Lowe, V; Pirko, I; Parisi, J E; Kantarci, K; Fields, J A; Bruns, M B; Boeve, B F; Lucchinetti, C F

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

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients

在帕金森病和病理确诊的路易体病患者中进行DNAJC13 p.Asn855Ser突变筛查

Lorenzo-Betancor, O; Ogaki, K; Soto-Ortolaza, A I; Labbe, C; Walton, R L; Strongosky, A J; van Gerpen, J A; Uitti, R J; McLean, P J; Springer, W; Siuda, J; Opala, G; Krygowska-Wajs, A; Barcikowska, M; Czyzewski, K; McCarthy, A; Lynch, T; Puschmann, A; Rektorova, I; Sanotsky, Y; Vilariño-Güell, C; Farrer, M J; Ferman, T J; Boeve, B F; Petersen, R C; Parisi, J E; Graff-Radford, N R; Dickson, D W; Wszolek, Z K; Ross, O A

Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

特邀综述:由微管相关蛋白tau基因(MAPT)突变引起的额颞叶痴呆:神经病理学和神经影像学的变色龙

Ghetti, B; Oblak, A L; Boeve, B F; Johnson, K A; Dickerson, B C; Goedert, M

Clinicopathologic correlations in 172 cases of rapid eye movement sleep behavior disorder with or without a coexisting neurologic disorder

对172例伴或不伴有神经系统疾病的快速眼动睡眠行为障碍患者的临床病理相关性分析

Boeve, B F; Silber, M H; Ferman, T J; Lin, S C; Benarroch, E E; Schmeichel, A M; Ahlskog, J E; Caselli, R J; Jacobson, S; Sabbagh, M; Adler, C; Woodruff, B; Beach, T G; Iranzo, A; Gelpi, E; Santamaria, J; Tolosa, E; Singer, C; Mash, D C; Luca, C; Arnulf, I; Duyckaerts, C; Schenck, C H; Mahowald, M W; Dauvilliers, Y; Graff-Radford, N R; Wszolek, Z K; Parisi, J E; Dugger, B; Murray, M E; Dickson, D W

Midbrain atrophy is not a biomarker of progressive supranuclear palsy pathology

中脑萎缩并非进行性核上性麻痹病理的生物标志物。

Whitwell, J L; Jack, C R Jr; Parisi, J E; Gunter, J L; Weigand, S D; Boeve, B F; Ahlskog, J E; Petersen, R C; Dickson, D W; Josephs, K A

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