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

Randomized Trial of Combined Aerobic, Resistance, and Cognitive Training to Improve Recovery From Stroke: Feasibility and Safety

一项随机对照试验研究了有氧运动、阻力训练和认知训练相结合对改善中风后康复的影响：可行性和安全性

期刊:Journal of the American Heart Association
影响因子:5.3
doi:10.1161/JAHA.119.015377
Koch, Sebastian; Tiozzo, Eduard; Simonetto, Marialaura; Loewenstein, David; Wright, Clinton B; Dong, Chuanhui; Bustillo, Antonio; Perez-Pinzon, Miguel; Dave, Kunjan R; Gutierrez, Carolina M; Lewis, John E; Flothmann, Marti; Mendoza-Puccini, M Carolina; Junco, Barbara; Rodriguez, Zuzel; Gomes-Osman, Joyce; Rundek, Tatjana; Sacco, Ralph L
中风
心血管
神经科学
发表日期：2020
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Cut-Off Values in the Prediction of Success in Olympic Distance Triathlon

奥运标准距离铁人三项成功预测中的临界值

期刊:International Journal of Environmental Research and Public Health
影响因子:
doi:10.3390/ijerph17249491
Gadelha, André Bonadias; Sousa, Caio Victor; Sales, Marcelo Magalhaes; Dos Santos Rosa, Thiago; Flothmann, Marti; Barbosa, Lucas Pinheiro; da Silva Aguiar, Samuel; Olher, Rafael Reis; Villiger, Elias; Nikolaidis, Pantelis Theodoros; Rosemann, Thomas; Hill, Lee; Knechtle, Beat
发表日期：2020
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Blockade of T-lymphocyte KCa3.1 and Kv1.3 channels as novel immunosuppression strategy to prevent kidney allograft rejection

阻断 T 淋巴细胞 KCa3.1 和 Kv1.3 通道作为预防肾移植排斥的新型免疫抑制策略

期刊:Transplantation Proceedings
影响因子:0.8
doi:10.1016/j.transproceed.2009.06.025
I Grgic, H Wulff, I Eichler, C Flothmann, R Köhler, J Hoyer
免疫
其它细胞
发表日期：2009
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Of maize and men. Is the endorsement of GM crops science or politics?

玉米与人类：对转基因作物的支持是出于科学还是政治考量？

期刊:EMBO Reports
影响因子:6.2
doi:10.1093/embo-reports/kve166
Flothmann, S; van Aken, J
发表日期：2001
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A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment

连接蛋白26听力障碍中常见的35delG GJB2基因突变的始祖

期刊:Journal of Medical Genetics
影响因子:3.5
doi:10.1136/jmg.38.8.515
L Van Laer，P Coucke, R F Mueller, G Caethoven, K Flothmann, S D Prasad, G P Chamberlin, M Houseman, G R Taylor, C M Van de Heyning, E Fransen, J Rowland, R A Cucci, R J Smith, G Van Camp
发表日期：2001
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Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Wolfram综合征1基因（WFS1）突变是低频感音神经性听力损失的常见原因。

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/10.22.2501
Bespalova, I N; Van Camp, G; Bom, S J; Brown, D J; Cryns, K; DeWan, A T; Erson, A E; Flothmann, K; Kunst, H P; Kurnool, P; Sivakumaran, T A; Cremers, C W; Leal, S M; Burmeister, M; Lesperance, M M
发表日期：2001
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