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期刊名:Acta neurologica belgica

缩写:ACTA NEUROL BELG

ISSN:0300-9009

e-ISSN:2240-2993

IF/分区:2.0/Q3

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共收录本刊相关文章索引3126条
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
Pegah Mohaghegh,Fardin Faraji,Afsoon Talaie Pegah Mohaghegh
Introduction: Identification of predictors associated with progression to Secondary progressive multiple sclerosis (SPMS) remains clinically important for optimizing long-term disease management. We aimed to evaluate demo...
Roberta Solazzi,Luca Andreoli,Susanna Fiori et al. Roberta Solazzi et al.
Functional Neurological Disorders (FNDs) are a frequent condition in childhood and adolescence, but data on hospitalized pediatric populations remain limited. In this study, we conducted a retrospective analysis of 136 pediatric patients (<...
Rafaella Theologou,Ioannis Tsechelidis,Artemios Artemiadis et al. Rafaella Theologou et al.
Introduction: Sensory ganglionopathy (SG) results from involvement of the dorsal root ganglia. Clinically, it presents with asymmetric, usually non-length-dependent, sensory symptoms, sensory ataxia and reduced or absent ...
Ioannis Mavroudis,Foivos Petridis,Dimitrios Kazis et al. Ioannis Mavroudis et al.
Visual complaints are common after mild traumatic brain injury (mTBI), yet the scope, assessment approaches, mechanisms, and rehabilitation strategies reported in the literature remain heterogeneous. To synthesize evidence on post-concussiv...
Buse Cagla Ari,Inci Emekli,Tugce Yaz et al. Buse Cagla Ari et al.
Background: Differentiating true normal pressure hydrocephalus (NPH) from neurodegenerative disorders with ex-vacuo ventriculomegaly remains a clinical challenge. Misdiagnosis can lead to inappropriate and risky shunt sur...
Mustafa Yıldız,Ece Meltem Yalçın,Abdurrahman Akgün et al. Mustafa Yıldız et al.
Objective: Vanishing White Matter Disease (VWM) is a rare autosomal recessive leukoencephalopathy caused by pathogenic variants in the EIF2B gene complex. This study aimed to describe the clinical, radiological, and genet...