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

Optical coherence tomography-based assessment of retinal vascular pathology in cerebral small vessel disease.

基于光学相干断层扫描的脑小血管病视网膜血管病变评估

Abdelhak A, Huss A, Brück A, Sebert U, Mayer B, Müller H P, Tumani H, Otto M, Yilmazer-Hanke D, Ludolph A C, Kassubek J, Pinkhardt E, Neugebauer H

Alcohol withdrawal syndrome: mechanisms, manifestations, and management

酒精戒断综合征:机制、表现和治疗

Jesse, S; Bråthen, G; Ferrara, M; Keindl, M; Ben-Menachem, E; Tanasescu, R; Brodtkorb, E; Hillbom, M; Leone, M A; Ludolph, A C

Fully automated atlas-based MR imaging volumetry in Huntington disease, compared with manual volumetry

亨廷顿病全自动基于图谱的磁共振成像体积测量与手动体积测量的比较

Kassubek, J; Pinkhardt, E H; Dietmaier, A; Ludolph, A C; Landwehrmeyer, G B; Huppertz, H-J

Alterations of the corpus callosum as an MR imaging-based hallmark of motor neuron diseases

胼胝体改变是运动神经元疾病的磁共振成像标志

Unrath, A; Ludolph, A C; Kassubek, J

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

伴有帕金森综合征的tau蛋白病:临床表现、神经病理学基础、生物标志物和治疗方案

Ludolph, A C; Kassubek, J; Landwehrmeyer, B G; Mandelkow, E; Mandelkow, E-M; Burn, D J; Caparros-Lefebvre, D; Frey, K A; de Yebenes, J G; Gasser, T; Heutink, P; Höglinger, G; Jamrozik, Z; Jellinger, K A; Kazantsev, A; Kretzschmar, H; Lang, A E; Litvan, I; Lucas, J J; McGeer, P L; Melquist, S; Oertel, W; Otto, M; Paviour, D; Reum, T; Saint-Raymond, A; Steele, J C; Tolnay, M; Tumani, H; van Swieten, J C; Vanier, M T; Vonsattel, J-P; Wagner, S; Wszolek, Z K

Cardiomyopathy in motor neuron diseases

运动神经元疾病中的心肌病

Gdynia, H-J; Kurt, A; Endruhn, S; Ludolph, A C; Sperfeld, A-D

Impaired RNA splicing of 5'-regulatory sequences of the astroglial glutamate transporter EAAT2 in human astrocytoma

人类星形胶质细胞瘤中星形胶质细胞谷氨酸转运蛋白EAAT2的5'调控序列RNA剪接受损

Münch, C; Penndorf, A; Schwalenstöcker, B; Troost, D; Ludolph, A C; Ince, P; Meyer, T

The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia

EAAT2 (GLT-1) 基因与运动神经元疾病:肌萎缩侧索硬化症中未发现突变,而遗传性痉挛性截瘫患者中存在点突变

Meyer, T; Münch, C; Völkel, H; Booms, P; Ludolph, A C