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期刊名:Journal of neurology

缩写:J NEUROL

ISSN:0340-5354

e-ISSN:1432-1459

IF/分区:4.6/Q1

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共收录本刊相关文章索引8811
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
Lucia Joffily,Lara Carvalho,Uroosa Mayet et al. Lucia Joffily et al.
Background and purpose: Patients with persistent postural-perceptual dizziness (PPPD) have comorbid low activity levels and the highest prevalence of poor sleep quality and insomnia across dizziness syndromes. Vestibular ...
Saidan Shetty,Yuting Luo,Aruna Thomas et al. Saidan Shetty et al.
Myotonic dystrophy type 1 (DM1) is a progressive neuromuscular disorder characterized by muscle weakness, fatigue, reduced endurance, and impaired quality of life. This systematic review and meta-analysis aimed to evaluate the effects of ex...
Melanie Haidegger,Natalie Berger,Simon Fandler-Höfler et al. Melanie Haidegger et al.
Background: Distinguishing posterior circulation stroke (PCS) from peripheral or other causes of acute vertigo can be challenging. Blood biomarkers, such as plasma neurofilament light chain (pNfL) and glial acidic fibrill...
Ignazio Giuseppe Arena,Shamini Saravanabavan,Rita Horvath et al. Ignazio Giuseppe Arena et al.
Primary mitochondrial diseases (PMDs) represent a clinically and genetically heterogeneous group of disorders characterized by impaired oxidative phosphorylation and multisystem involvement, commonly affecting the nervous system. As therape...
Harald Hegen,Fabian Föttinger,Janette Walde et al. Harald Hegen et al.
Background: Treatment strategy for relapsing multiple sclerosis (RMS) is increasingly shifting toward first-line use of high-efficacy DMT (H-DMT). However, differences in DMT efficacy appear to decline with increasing age...
Leire Manrique,Francisco Martínez-Dubarbie,Ana L Pelayo-Negro et al. Leire Manrique et al.
Friedreich's ataxia (FRDA) is the most common early onset hereditary ataxia, caused by GAA repeat expansions in the FXN gene. The length of the shorter allele (GAA1) and age at onset are established determinants of disease severity, though ...
Daniel S Marín-Medina,Joselyn Miño Zambrano,Alberto J Espay et al. Daniel S Marín-Medina et al.
Background: Misdiagnosis of functional movement disorders (FMD) remains a concern for clinicians. We sought to review the phenomenology and clinical features associated with FMD misdiagnosis. ...
S Jarius,K Ruprecht,I Metz et al. S Jarius et al.
Recently, an autoantibody signature considered to be predictive of multiple sclerosis (MS) has been reported in an article by Zamecnik et al. published in Nature Medicine, which is characterized by immunoglobulin G (IgG) responses to peptid...