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期刊名:Journal of central nervous system disease

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ISSN:1179-5735

e-ISSN:1179-5735

IF/分区:2.8/Q2

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共收录本刊相关文章索引288
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
Chiara Höhler,Joachim Hermsdörfer,Klaus Jahn et al. Chiara Höhler et al.
Background: After standard care, 55%-75% of patients after stroke show a persistent paresis of the upper limb (UL). Assistive devices are developed to increase the patients' level of independence in daily life. ...
Jiwon Oh,Paul S Giacomini,V Wee Yong et al. Jiwon Oh et al.
Significant advances have been made in the diagnosis and treatment of multiple sclerosis in recent years yet challenges remain. The current classification of MS phenotypes according to disease activity and progression, for example, does not...
Christoph Friedli,Nik Krajnc,Helly N Hammer et al. Christoph Friedli et al.
Introduction: Patients with Multiple Sclerosis (pwMS) treated with anti-CD20 (cluster of differentiation) monoclonal antibodies (mAbs) such as ocrelizumab (OCR) and ofatumumab (OFA) show a reduction mainly of B-lymphocyte...
Christoph Waiß,Barbara Ströbele,Uwe Graichen et al. Christoph Waiß et al.
Background: 'Definite Neuroborreliosis (NB)' is diagnosed with the presence of NB-specific symptoms, cerebrospinal fluid (CSF) pleocytosis and an elevated Borrelia Burgdorferi antibody index. However, some diagnostic unce...
Areej Turkistani,Hayder M Al-Kuraishy,Ali I Al-Gareeb et al. Areej Turkistani et al.
Epilepsy is a chronic neurological disorder manifested by recurring unprovoked seizures resulting from an imbalance in the inhibitory and excitatory neurotransmitters in the brain. The process of epileptogenesis involves a complex interplay...
Noor Redha,Zahra Al-Sahlawi,Hasan Hasan et al. Noor Redha et al.
MNGIE (Mitochondrial Neurogastrointestinal Encephalomyopathy) is an ultra-rare autosomal recessive disorder that leads to mutations in the nuclear genes encoding thymidine phosphorylase. Symptoms include gastrointestinal dysmotility, cachex...
Hareesha R Bharadwaj,Wireko A Awuah,Favour T Adebusoye et al. Hareesha R Bharadwaj et al.
BACKGROUND: Awake craniotomy has emerged as an advanced surgical technique, characterized by keeping the patient awake during brain surgery. In South America, awake craniotomies have grained traction in neurosurgical practices across variou...
Di Wang,Di Lu,Mingtai Zhang et al. Di Wang et al.
Hypothalamic hamartomas (HHs) are congenital developmental malformations located in the hypothalamus. They are associated with a characteristic clinical manifestation known as gelastic seizures (GS). However, the traditional understanding o...
Monique Anderson,Michael Levy Monique Anderson
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune neuroinflammatory disorder with a prevalence of 1-5/100,000 globally, characterized by attacks of the central nervous system including but not limited to optic neuritis, tr...