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

Progressive Supranuclear Palsy-A Global Review

进行性核上性麻痹症——全球综述

Kukkle, Prashanth Lingappa; Neupane, Rosy; Pantelyat, Alexandar; Wills, Anne-Marie; Jabbari, Ed; Dopper, Elise G P; Kovacs, Gabor G; Hoglinger, Gunther; Aiba, Ikuko; Litvan, Irene; Ganguly, Jacky; Whitwell, Jennifer L; Ma, Jinghong; Okeng'O, Kigocha; Skakibara, Ryuji; Forrest, Shelley; Lorenzl, Stefan; Zewde, Yared Zenebe; Compta, Yaroslau; Morris, Huw R

Multiple System Atrophy Without Dysautonomia: An Autopsy-Confirmed Study

无自主神经功能障碍的多系统萎缩:一项尸检证实的研究

Wilkens, Ida; Bebermeier, Sarah; Heine, Johanne; Ruf, Viktoria Constanze; Compta, Yaroslau; Molina Porcel, Laura; Troakes, Claire; Vamanu, Albert; Downes, Sophia; Irwin, David John; Cohen, Jesse; Lee, Edward B; Nilsson, Christer F; Englund, Elisabet M; Nemati, Mojtaba; Katzdobler, Sabrina; Levin, Johannes; Bernhardt, Alexander Maximilian; Pantelyat, Alexander; Seemiller, Joseph; Berger, Stephen; Van Swieten, John C; Dopper, Elise G P; Rozemuller, Annemieke J M; Kovacs, Gabor G; Bendahan, Nathaniel; Lang, Anthony E; Herms, Jochen; Höglinger, Günter U; Hopfner, Franziska

Montreal Cognitive Assessment vs the Mini-Mental State Examination as a Screening Tool for Patients With Genetic Frontotemporal Dementia

蒙特利尔认知评估与简易精神状态检查作为遗传性额颞叶痴呆患者筛查工具的比较

de Boer, Liset; Poos, Jackie M; Van Den Berg, Esther; De Houwer, Julie F H; Swartenbroekx, Tine; Dopper, Elise G P; Boesjes, Pam; Tahboun, Najlae; Bouzigues, Arabella; Foster, Phoebe H; Ferry-Bolder, Eve; Adams-Carr, Kerala; Russell, Lucy L; Convery, Rhian S; Rohrer, Jonathan D; Seelaar, Harro; Jiskoot, Lize C

Quantitative MRI-based decision model for early-stage parkinsonism diagnosis: a pilot feasibility study

基于定量磁共振成像的早期帕金森病诊断决策模型:一项初步可行性研究

Nunez-Gonzalez, Laura; Dopper, Elise G P; van der Eerden, Anke W; Seada, Samy Abo; Boon, Agnita J W; Verbeek, Marcel M; Bloem, Bastiaan R; Anton Meijer, Frederick Jan; Hernandez-Tamames, Juan Antonio

Investigating the role of neuroinflammation and brain clearance in frontotemporal lobar degeneration using 7T MRI and fluid biomarkers: protocol for a cross-sectional study in a tertiary care setting

利用7T磁共振成像和体液生物标志物研究神经炎症和脑组织清除在额颞叶变性中的作用:一项在三级医疗机构开展的横断面研究方案

Prinse, Fieke A M; van der Weerd, Louise; van Swieten, John C; Ronen, Itamar; Seelaar, Harro; Hirschler, Lydiane; Najac, Chloé; Dopper, Elise G P

Neuropsychological Profiles in Genetic Frontotemporal Dementia: A Meta-Analysis and Systematic Review

遗传性额颞叶痴呆的神经心理学特征:一项荟萃分析和系统综述

Poos, Jackie M; van den Berg, Esther; de Boer, Liset; Meertens-Gunput, Sabrina; Dopper, Elise G P; Seelaar, Harro; Jiskoot, Lize C

Two novel variants in GRN: the relevance of CNV analysis and genetic screening in FTLD patients with a negative family history

GRN基因的两个新变异:拷贝数变异分析和基因筛查在无家族史的额颞叶痴呆患者中的意义

De Houwer, Julie F H; Dopper, Elise G P; Rajicic, Ana; van Buuren, Renee; Arcaro, Marina; Galimberti, Daniela; Breedveld, Guido J; Wilke, Martina; van Minkelen, Rick; Jiskoot, Lize C; van Swieten, John C; Donker Kaat, Laura; Seelaar, Harro

Clinical Value of Longitudinal Serum Neurofilament Light Chain in Prodromal Genetic Frontotemporal Dementia

纵向血清神经丝轻链在遗传性额颞叶痴呆前驱期中的临床价值

Giannini, Lucia A A; Seelaar, Harro; van der Ende, Emma L; Poos, Jackie M; Jiskoot, Lize C; Dopper, Elise G P; Pijnenburg, Yolande A L; Willemse, Eline A J; Vermunt, Lisa; Teunissen, Charlotte E; van Swieten, John C; Meeter, Lieke H

Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia

模拟GRN相关额颞叶痴呆症中生物标志物变化的级联

Panman, Jessica L; Venkatraghavan, Vikram; van der Ende, Emma L; Steketee, Rebecca M E; Jiskoot, Lize C; Poos, Jackie M; Dopper, Elise G P; Meeter, Lieke H H; Donker Kaat, Laura; Rombouts, Serge A R B; Vernooij, Meike W; Kievit, Anneke J A; Premi, Enrico; Cosseddu, Maura; Bonomi, Elisa; Olives, Jaume; Rohrer, Jonathan D; Sánchez-Valle, Raquel; Borroni, Barbara; Bron, Esther E; Van Swieten, John C; Papma, Janne M; Klein, Stefan

Distinctive pattern of temporal atrophy in patients with frontotemporal dementia and the I383V variant in TARDBP

额颞叶痴呆患者颞叶萎缩模式独特,且携带TARDBP基因I383V变异。

Mol, Merel O; Nijmeijer, Sebastiaan W R; van Rooij, Jeroen G J; van Spaendonk, Resie M L; Pijnenburg, Yolande A L; van der Lee, Sven J; van Minkelen, Rick; Donker Kaat, Laura; Rozemuller, Annemieke J M; Janse van Mantgem, Mark R; van Rheenen, Wouter; van Es, Michael A; Veldink, Jan H; Hennekam, Frederic A M; Vernooij, Meike; van Swieten, John C; Cohn-Hokke, Petra E; Seelaar, Harro; Dopper, Elise G P