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

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers

利用肌肉蛋白质组学和血清生物标志物探索PURA综合征的分子特征

Mroczek, Magdalena; Preusse, Corinna; Hentschel, Andreas; Chrościńska-Krawczyk, Magdalena; Bielak, Michał; Sobolewska, Adela; Della Marina, Adela; Hila, Anisa; Iyadurai, Stanley; Kraft, Florian; Chetty, Venkatesh Kumar; Muhmann, David; Ruck, Tobias; Goebel, Hans-Hilmar; Schara-Schmidt, Ulrike; Dobelmann, Vera; Thakur, Basant Kumar; Stenzel, Werner; Roos, Andreas

The p.(Leu97Ile) variant expands the genetic landscape of NEFL-associated Charcot-Marie-tooth neuropathies

p.(Leu97Ile)变异扩展了NEFL相关夏科-马里-图斯神经病的遗传图谱

Oeztuerk, Menekse; Walli, Sara; Muhmann, David; Choueiri, Catherine; Dobelmann, Vera; Abicht, Angela; Leube, Barbara; Schara-Schmidt, Ulrike; Meuth, Sven G; Horvath, Rita; Lochmueller, Hanns; Roos, Andreas; Ruck, Tobias

Glenoid Radiolucent Lines and Subsidence Show Limited Impact on Clinical and Functional Long-Term Outcomes After Anatomic Total Shoulder Arthroplasty: A Retrospective Analysis of Cemented Polyethylene Glenoid Components

肩胛盂透亮线和沉降对解剖型全肩关节置换术后的临床和功能长期结果影响有限:一项对骨水泥型聚乙烯肩胛盂假体的回顾性分析

Hochberger, Felix; Limmer, Jonas; Muhmann, Justus; Gohlke, Frank; Streck, Laura Elisa; Rudert, Maximilian; List, Kilian

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report

组织学和蛋白质组学联合分析揭示KMT5B相关神经发育障碍中的肌肉去神经支配:病例报告

Aksel Kilicarslan, Ozge; Gangfuß, Andrea; Kölbel, Heike; Muhmann, David; Polavarapu, Kiran; Thompson, Rachel; Schmitt, Linda-Isabell; Lessard, Lola; Chen, Lei; Eisenkölbl, Astrid; Schara-Schmidt, Ulrike; Hentschel, Andreas; Lochmüller, Hanns; Roos, Andreas

[Not Available]

[无法使用]

Muhmann, David; Droste, Marvin; Schulz, Jörn; Linge, Frederike; Ladewig, Lea; Eisenberg, Ursula; Röder, Susanne; Büscher, Rainer; Diener, Hans-Christoph