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

Improved Alzheimer's Disease versus Frontotemporal Lobar Degeneration Differential Diagnosis Combining EEG and Neurochemical Biomarkers: A Pilot Study

结合脑电图和神经化学生物标志物改进阿尔茨海默病与额颞叶变性的鉴别诊断：一项初步研究

期刊:Journal of Alzheimers Disease
影响因子:3.1
doi:10.3233/JAD-220693
Laton, Jorne; Van Schependom, Jeroen; Goossens, Joery; Wiels, Wietse; Sieben, Anne; De Deyn, Peter Paul; Goeman, Johan; Streffer, Johannes; van der Zee, Julie; Martin, Jean-Jacques; Van Broeckhoven, Christine; De Vos, Maarten; Bjerke, Maria; Nagels, Guy; Engelborghs, Sebastiaan
阿尔茨海默症
神经科学
发表日期：2022
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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease

罕见的纯合和复合杂合VPS13C错义突变对路易体痴呆和帕金森病的影响

期刊:Acta Neuropathologica Communications
影响因子:5.7
doi:10.1186/s40478-021-01121-w
Smolders, Stefanie; Philtjens, Stéphanie; Crosiers, David; Sieben, Anne; Hens, Elisabeth; Heeman, Bavo; Van Mossevelde, Sara; Pals, Philippe; Asselbergh, Bob; Dos Santos Dias, Roberto; Vermeiren, Yannick; Vandenberghe, Rik; Engelborghs, Sebastiaan; De Deyn, Peter Paul; Martin, Jean-Jacques; Cras, Patrick; Annaert, Wim; Van Broeckhoven, Christine
帕金森
神经科学
发表日期：2021
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Validation of the Erlangen Score Algorithm for Differential Dementia Diagnosis in Autopsy-Confirmed Subjects

对尸检确诊病例中埃尔兰根评分算法进行痴呆症鉴别诊断的验证

期刊:Journal of Alzheimers Disease
影响因子:3.1
doi:10.3233/JAD-180563
Somers, Charisse; Lewczuk, Piotr; Sieben, Anne; Van Broeckhoven, Christine; De Deyn, Peter Paul; Kornhuber, Johannes; Martin, Jean-Jacques; Bjerke, Maria; Engelborghs, Sebastiaan
发表日期：2019
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GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia

GDAP2基因突变与一种新型小脑共济失调中细胞应激易感性有关。

期刊:Brain
影响因子:11.7
doi:10.1093/brain/awy198
Eidhof, Ilse; Baets, Jonathan; Kamsteeg, Erik-Jan; Deconinck, Tine; van Ninhuijs, Lisa; Martin, Jean-Jacques; Schüle, Rebecca; Züchner, Stephan; De Jonghe, Peter; Schenck, Annette; van de Warrenburg, Bart P
细胞生物学
神经科学
发表日期：2018
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Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family

扩展的FTLD家系分离出比利时GRN基因缺失突变：一个家族中的神经病理学异质性

期刊:Alzheimers Research & Therapy
影响因子:7.6
doi:10.1186/s13195-017-0334-y
Sieben, Anne; Van Mossevelde, Sara; Wauters, Eline; Engelborghs, Sebastiaan; van der Zee, Julie; Van Langenhove, Tim; Santens, Patrick; Praet, Marleen; Boon, Paul; Miatton, Marijke; Van Hoecke, Sofie; Vandenbulcke, Mathieu; Vandenberghe, Rik; Cras, Patrick; Cruts, Marc; De Deyn, Peter Paul; Van Broeckhoven, Christine; Martin, Jean-Jacques
发表日期：2018
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Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration

脑脊液tau蛋白、神经丝蛋白和前粒蛋白在确诊额颞叶变性中的诊断价值

期刊:Alzheimers Research & Therapy
影响因子:7.6
doi:10.1186/s13195-018-0364-0
Goossens, Joery; Bjerke, Maria; Van Mossevelde, Sara; Van den Bossche, Tobi; Goeman, Johan; De Vil, Bart; Sieben, Anne; Martin, Jean-Jacques; Cras, Patrick; De Deyn, Peter Paul; Van Broeckhoven, Christine; van der Zee, Julie; Engelborghs, Sebastiaan
神经科学
发表日期：2018
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Added Diagnostic Value of Cerebrospinal Fluid Biomarkers for Differential Dementia Diagnosis in an Autopsy-Confirmed Cohort

脑脊液生物标志物在尸检确诊队列中对痴呆症鉴别诊断的附加诊断价值

期刊:Journal of Alzheimers Disease
影响因子:3.1
doi:10.3233/JAD-170927
Niemantsverdriet, Ellis; Feyen, Bart F E; Le Bastard, Nathalie; Martin, Jean-Jacques; Goeman, Johan; De Deyn, Peter Paul; Bjerke, Maria; Engelborghs, Sebastiaan
神经科学
发表日期：2018
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No added diagnostic value of non-phosphorylated tau fraction (p-tau(rel)) in CSF as a biomarker for differential dementia diagnosis

脑脊液中非磷酸化tau蛋白（p-tau(rel)）作为痴呆症鉴别诊断的生物标志物，并无额外的诊断价值。

期刊:Alzheimers Research & Therapy
影响因子:7.6
doi:10.1186/s13195-017-0275-5
Goossens, Joery; Bjerke, Maria; Struyfs, Hanne; Niemantsverdriet, Ellis; Somers, Charisse; Van den Bossche, Tobi; Van Mossevelde, Sara; De Vil, Bart; Sieben, Anne; Martin, Jean-Jacques; Cras, Patrick; Goeman, Johan; De Deyn, Peter Paul; Van Broeckhoven, Christine; van der Zee, Julie; Engelborghs, Sebastiaan
信号转导
磷酸化
神经科学
发表日期：2017
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Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

散发性迟发性线状肌病：临床病理特征及76例病例回顾

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-017-0640-2
Schnitzler, Lukas J; Schreckenbach, Tobias; Nadaj-Pakleza, Aleksandra; Stenzel, Werner; Rushing, Elisabeth J; Van Damme, Philip; Ferbert, Andreas; Petri, Susanne; Hartmann, Christian; Bornemann, Antje; Meisel, Andreas; Petersen, Jens A; Tousseyn, Thomas; Thal, Dietmar R; Reimann, Jens; De Jonghe, Peter; Martin, Jean-Jacques; Van den Bergh, Peter Y; Schulz, Jörg B; Weis, Joachim; Claeys, Kristl G
发表日期：2017
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Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

比利时人群中TBK1基因携带者与C9orf72、GRN基因携带者和非突变携带者的临床特征比较

期刊:Brain
影响因子:11.7
doi:10.1093/brain/awv358
Van Mossevelde, Sara; van der Zee, Julie; Gijselinck, Ilse; Engelborghs, Sebastiaan; Sieben, Anne; Van Langenhove, Tim; De Bleecker, Jan; Baets, Jonathan; Vandenbulcke, Mathieu; Van Laere, Koen; Ceyssens, Sarah; Van den Broeck, Marleen; Peeters, Karin; Mattheijssens, Maria; Cras, Patrick; Vandenberghe, Rik; De Jonghe, Peter; Martin, Jean-Jacques; De Deyn, Peter P; Cruts, Marc; Van Broeckhoven, Christine
TBK1
发表日期：2016
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