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Katrin Hahn

Charité - Universitätsmedizin Berlin
H指数:30
被引数:2,789

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Biallelic PIGB Variants Cause Motor Neuropathy with Conduction Blocks and Peripheral Nerve Hyperexcitability

PIGB基因双等位基因变异导致伴有传导阻滞和周围神经高兴奋性的运动神经病变

2026-10-010
OAAI
Specific treatment of ATTR-CM in Germany—expert consensus of the German Society of Amyloid Diseases (DGAK) and German Cardiac Society (DGK)

德国ATTR-CM的特异性治疗——德国淀粉样变性病学会(DGAK)和德国心脏学会(DGK)专家共识

2026-09-220
OAAI
Disease modifying treatment of hereditary transthyretin amyloidosis with polyneuropathy in Germany – expert consensus of the German society of amyloid diseases (DGAK) and the German neurological society (DGN)

德国遗传性甲状腺素转运蛋白淀粉样变性伴多发性神经病变的疾病修饰治疗——德国淀粉样变性学会(DGAK)和德国神经病学学会(DGN)的专家共识

2026-08-110
OAAI
ePA4all—Exploring facilitators and barriers to the adoption of the electronic health record in Germany: A study protocol for a mixed-methods analysis

ePA4all—探索电子健康记录在德国推广的促进因素和阻碍因素:一项混合方法分析的方案研究

2026-02-190
PRE
Real-world treatment management in hereditary transthyretin amyloidosis – an experience report and proposal for therapy switch decision criteria

现实世界中遗传性甲状腺素转运蛋白淀粉样变性病的治疗管理——一份经验报告及治疗转换决策标准的建议

2025-09-120
OA
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD

由于SORD基因突变导致的Charcot-Marie-Tooth疾病的基因型与表型谱

BRAIN
IF11.7
2025-08-013
OAAI
Mitochondrial damage is associated with an early immune response in inclusion body myositis

线粒体损伤与包涵体肌炎的早期免疫反应相关

Brain
IF11.7
2025-04-070
PRE
Real-world characteristics and treatment of cardiac transthyretin amyloidosis: A multicentre, observational study

心脏转甲状腺素蛋白淀粉样变性的真实世界特征和治疗: 一项多中心观察性研究

2024-11-060
OA
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants

遗传性转甲状腺素蛋白相关淀粉样变性正在进行的观察性研究: 前3167名参与者的基线报告

2024-10-170
OAAI