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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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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
Lazaros C Triarhou Lazaros C Triarhou
The article revisits neurobiological experiments conducted over the past 50 years, aimed at deciphering questions of cerebellar development and plasticity, and the integration of primordial cerebellar tissue into host brains by means of int...
Xiaoyang Li,Pranjal Gupta,Naveen K Paramasivan et al. Xiaoyang Li et al.
Background: Anti-LGI1 autoimmune encephalitis is an immunotherapy-responsive condition with growing interest in clinical trial development. However, the lack of reliable outcome measures is a major barrier. We aim to desi...
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Background: Plasma neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) are promising blood-based biomarkers of neuroaxonal injury and astrocytic activation, relevant in neurodegeneration. We investi...
M Trojano,P Iaffaldano,M Copetti et al. M Trojano et al.
Objective: The objective of this study is to present a report from the Big Multiple Sclerosis Data (BMSD) statistics workshop (Bari - Italy, June 2023) which focused on advanced statistical approaches for real-world data ...
Carolina Barnett-Tapia,Elena Cortés Vicente,Robert M Pascuzzi et al. Carolina Barnett-Tapia et al.
Background: Generalized myasthenia gravis (gMG) is an autoimmune disease characterized by fluctuating muscle weakness. The MG Impairment Index (MGII) incorporates patients' perspectives (22 items) and physician evaluation...
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Inherited cerebellar ataxias (ICA) are a group of rare, genetically and clinically heterogeneous neurodegenerative disorders, often caused by a broad spectrum of genetic variants, including single nucleotide variants, structural variations,...
Serkan Ozakbaş,Said Alizada,Can Caliskan et al. Serkan Ozakbaş et al.
Background: Familial multiple sclerosis (MS), defined by the occurrence of MS in one or more relatives, is thought to represent a genetically influenced subtype of the disease. ...
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Background: Freezing of gait (FOG) in Parkinson's disease (PD) is a disabling motor symptom with unclear pathophysiology. Beyond known basal ganglia dysfunction and cognitive impairment, sensory integration deficits are i...