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期刊名:European journal of neurology

缩写:EUR J NEUROL

ISSN:1351-5101

e-ISSN:1468-1331

IF/分区:4.3/Q1

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共收录本刊相关文章索引7024
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
A Guérémy,E Fortanier,C P Michel et al. A Guérémy et al.
Objective: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is characterized by heterogeneous clinical presentations and the absence of validated imaging biomarkers. Although several quantitative MRI (qMRI...
Yusuf A Rajabally,Joumana Freiha,Roshan Iqbal et al. Yusuf A Rajabally et al.
Background: Whether serial electrophysiology may be useful in chronic inflammatory demyelinating polyneuropathy (CIDP), in remission off treatment, is unknown. ...
Anna Kufner,Yunyou Tang,Uchralt Temuulen et al. Anna Kufner et al.
Background: Falls affect over 30% of stroke survivors within the first year, yet lesion-related mobility and gait impairments underlying fall risk remain poorly understood. This study aimed to identify lesion-derived func...
Constantina Rodica Popa,Dominique Hervé,Nassira Alili et al. Constantina Rodica Popa et al.
Background and purpose: Familial cerebral cavernous malformations (fCCM) may cause focal neurological deficits (FND) due to hemorrhagic or non-hemorrhagic events and epileptic seizures (ES). With the widespread use of mag...
Nilo Riva,Paride Schito,Tommaso Russo et al. Nilo Riva et al.
Background: Respiratory failure is the main cause of death in Amyotrophic lateral sclerosis (ALS), in which the physiological sigh reflex is impaired due to inspiratory muscle weakness. Aim of this study is to assess the ...
Dror Shir,Noa Bregman,Aya Bar David et al. Dror Shir et al.
Background: Genetic Creutzfeldt-Jakob Disease (gCJD) is an autosomal dominant prion disease caused by heterozygous pathogenic variants in the PRNP gene. It is relatively prevalent in Israel due to a large cluster of indiv...
Patrick Vermersch,Ralph H B Benedict,Bart Van Wijmeersch et al. Patrick Vermersch et al.
Background: Almost 75% of patients with relapsing multiple sclerosis (pwRMS) with suboptimal response to other disease-modifying therapies (DMTs) showed no evidence of disease activity (NEDA-3) when treated with ocrelizum...
Francesco Favruzzo,Marialuisa Zedde,Luca Weis et al. Francesco Favruzzo et al.
Background and aims: The safety and effectiveness of mechanical thrombectomy (MT) in patients with cervical artery dissection (CeAD) remain uncertain. This study aimed to evaluate the safety, recanalization rates, and fun...
Robin van Pinxteren,Marilien C Marzolla,Melloney L M Wijenberg et al. Robin van Pinxteren et al.
Background: While most people fully recover after mild traumatic brain injury (mTBI), a substantial minority experience persistent symptoms and incomplete recovery. This may be prevented by early interventions specificall...
Paulo Bastos,Marc Kermorgant,Fabienne Ory-Magne et al. Paulo Bastos et al.
Background: Multiple system atrophy (MSA) is characterized by progressive autonomic/motor dysfunction, but robust biomarkers do not exist. Electrochemical skin conductance (ESC) provides a noninvasive measure of sudomotor...