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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7059
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
Maiju Savolainen,Merja Soilu-Hänninen,Henriikka Nurmi et al. Maiju Savolainen et al.
Background: B-cell-depleting anti-CD20 therapies are among the most effective disease-modifying treatments for relapsing-remitting multiple sclerosis (RRMS). Rituximab (RTX) is widely used off-label, while ocrelizumab (OC...
Lin Bai,Haitao Ren,Qiang Lu et al. Lin Bai et al.
Object: Glutamic acid decarboxylase antibody-associated neurological disease (GADAND) is a rare autoimmune disorder with elusive immunogenetic underpinnings. We aimed to investigate HLA associations with GADAND susceptibi...
Filipa Bastos,Davide Strambo,Alexander Salerno et al. Filipa Bastos et al.
Background and purpose: Functional stroke-like episodes (FSMs) are an increasingly recognised stroke mimic with demographic and clinical characteristics that differ from acute ischaemic strokes (AISs) but have unclear lon...
Vest Teresa,Verho Liisa,Rantanen Kirsi et al. Vest Teresa et al.
Background: Posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS) are related neurovascular conditions, with pregnancy as a shared risk factor. In this study, we aime...
Loredana Storelli,Damiano Mistri,Alice Mastropasqua et al. Loredana Storelli et al.
Background: Cognitive impairment is common in multiple sclerosis (MS), yet the application of diagnostic frameworks of Neurocognitive Disorders (NCDs) is limited. Additionally, the integration of multimodal data for predi...
Yaqiong Ren,Yue Cao,Fangfang Cheng et al. Yaqiong Ren et al.
Background: Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive disorder caused by variants in the NTRK1 gene (encoding TrkA). The identification and functional analysis of these variants are...
Marcello Silvestro,Ilaria Orologio,Raffaele Ornello et al. Marcello Silvestro et al.
Background: Although treatment goals in migraine prevention have moved beyond the benchmark of a 50% reduction in monthly attacks, residual disease burden is still evaluated based on residual headache frequency. However, ...
Paul Philipp Kastner,Pia Lena Niederau,Georgios Pantazis et al. Paul Philipp Kastner et al.
Background: Subacute oculomotor dysfunction encompasses a broad differential diagnosis, including autoimmune, infectious, vascular, and neoplastic etiologies. Primary skull base diffuse large B-cell lymphoma (DLBCL) is a ...
Jean-Philippe Camdessanche,Andoni Echaniz-Laguna,Guilhem Solé et al. Jean-Philippe Camdessanche et al.
Background: The French National Rare Diseases Registry (BNDMR) was established in 2007 to ensure access to optimal care standards for all patients with rare diseases in dedicated reference centres. The objective of this r...