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

Paxilline Prevents the Onset of Myotonic Stiffness in Pharmacologically Induced Myotonia: A Preclinical Investigation

帕西林可预防药物诱发的肌强直引起的肌强直发作:一项临床前研究

Kerstin Hoppe, Tina Sartorius, Sunisa Chaiklieng, Georg Wietzorrek, Peter Ruth, Karin Jurkat-Rott, Scott Wearing, Frank Lehmann-Horn, Werner Klingler0

Fascial tissue research in sports medicine: from molecules to tissue adaptation, injury and diagnostics: consensus statement

运动医学中的筋膜组织研究:从分子到组织适应、损伤和诊断:共识声明

Zügel, Martina; Maganaris, Constantinos N; Wilke, Jan; Jurkat-Rott, Karin; Klingler, Werner; Wearing, Scott C; Findley, Thomas; Barbe, Mary F; Steinacker, Jürgen Michael; Vleeming, Andry; Bloch, Wilhelm; Schleip, Robert; Hodges, Paul William

Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients

罕见的KCNJ18变异并不能解释263例互不相关的患者出现的低钾性周期性麻痹。

Kuhn, Marius; Jurkat-Rott, Karin; Lehmann-Horn, Frank

Early-onset familial hemiplegic migraine due to a novel SCN1A mutation

由新型SCN1A突变引起的早发性家族性偏瘫性偏头痛

Fan, Chunxiang; Wolking, Stefan; Lehmann-Horn, Frank; Hedrich, Ulrike Bs; Freilinger, Tobias; Lerche, Holger; Borck, Guntram; Kubisch, Christian; Jurkat-Rott, Karin

Hypermetabolism in B-lymphocytes from malignant hyperthermia susceptible individuals

恶性高热症易感人群的 B 淋巴细胞代谢亢进

Kerstin Hoppe, Guido Hack, Frank Lehmann-Horn, Karin Jurkat-Rott, Scott Wearing, Alberto Zullo, Antonella Carsana, Werner Klingler

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

SCN4A孔道突变是常染色体显性遗传性特发性震颤的致病因素之一,并可能增加癫痫的易感性。

Bergareche, Alberto; Bednarz, Marcin; Sánchez, Elena; Krebs, Catharine E; Ruiz-Martinez, Javier; De La Riva, Patricia; Makarov, Vladimir; Gorostidi, Ana; Jurkat-Rott, Karin; Marti-Masso, Jose Felix; Paisán-Ruiz, Coro

Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathy

骨骼肌钠通道病中的二价阳离子反应性肌强直和肌肉麻痹

Mankodi, Ami; Grunseich, Christopher; Skov, Martin; Cook, Lisa; Aue, Georg; Purev, Enkhtsetseg; Bakar, Dara; Lehky, Tanya; Jurkat-Rott, Karin; Pedersen, Thomas H; Childs, Richard W

Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre study

临床恶性高热危象的功能和遗传特征:一项多中心研究

Klingler, Werner; Heiderich, Sebastian; Girard, Thierry; Gravino, Elvira; Heffron, James Ja; Johannsen, Stephan; Jurkat-Rott, Karin; Rüffert, Henrik; Schuster, Frank; Snoeck, Marc; Sorrentino, Vincenzo; Tegazzin, Vincenzo; Lehmann-Horn, Frank

Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutation

结构域 III S4 在闭合状态下的快速失活:来自周期性麻痹突变的启示

Groome, James R; Jurkat-Rott, Karin; Lehmann-Horn, Frank

Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita

致病突变 C277R 和 C277Y 改变了先天性肌强直症中人类 ClC-1 氯离子通道的门控

Sebastian Weinberger, Daniel Wojciechowski, Damien Sternberg, Frank Lehmann-Horn, Karin Jurkat-Rott, Toni Becher, Birgit Begemann, Christoph Fahlke, Martin Fischer