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期刊名:Childs nervous system

缩写:CHILD NERV SYST

ISSN:0256-7040

e-ISSN:1433-0350

IF/分区:1.3/Q3

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共收录本刊相关文章索引6660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
Luís Felipe Ribeiro Soares,Fernanda Moraes Daniel Fialho,Nathalia Grigorovski de Almeida Kuyven et al. Luís Felipe Ribeiro Soares et al.
Background: Pediatric neurocritical care (PNC) has emerged as a specialized field aimed at improving outcomes for children with neurological conditions. Despite advances, pediatric neuro-oncology remains underrepresented ...
Raashid Hamid,Kashif Qureshi,Mohsin Fayaz et al. Raashid Hamid et al.
Background: Occult spinal dysraphism (OSD) represents a group of congenital spinal anomalies in which neural tissue remains covered by intact skin. Because the skin and nervous system share a common ectodermal origin, mid...
Valentina Ponchio,Reem Hussin,Wassim Harati et al. Valentina Ponchio et al.
Cerebral arteriovenous malformations (AVMs) and congenital heart diseases (CHDs) are rare, complex conditions that often present diagnostic and therapeutic challenges-especially when they coexist in pediatric patients. Though individually u...
Mohit Agrawal,Sarbesh Tiwari,Swati Chhabra et al. Mohit Agrawal et al.
Background: KMT2B-related dystonia (DYT-28) is a recently recognized cause of early-onset generalized dystonia. Pallidal deep brain stimulation (GPi-DBS) is considered the preferred surgical treatment; however, access, co...
Anıl Erol,Cihat Karagöz,Larisa Andrada Ay et al. Anıl Erol et al.
Intracranial pseudoaneurysms (IPAs) account for less than 1% of all intracranial aneurysms, yet they have been reported more frequently in the pediatric population, carrying a high risk of morbidity and mortality. Giant IPAs in children are...
Amparo Saenz,Honglin Zhu,Jasneet Dhaliwal et al. Amparo Saenz et al.
Background: Pediatric complex Chiari I Malformation (CCM), defined by Chiari I with additional craniovertebral junction anomalies, has been associated with higher failure rates following foramen magnum decompression (FMD)...
Eleonora Visocchi,Manuel Camelia,Chiara Spezzani et al. Eleonora Visocchi et al.
Primary intraosseous meningiomas (PIOMs) are rare extradural meningiomas, originating within the skull, and accounting for approximately 2% of all meningiomas. These tumors are exceptionally uncommon in children, since the majority occurs i...
Kusawadee Juengsirakulwit,Jiraphorn Amornfa Kusawadee Juengsirakulwit
Introduction: Postoperative wound complications - including surgical site infection (SSI), cerebrospinal fluid (CSF) leakage, and wound dehiscence - remain a significant challenge following surgery for spinal dysraphism, ...
Omar Alomari,Rana Al Juhmani,Beyzanur Güney et al. Omar Alomari et al.
Background and aim: Chiari malformation type 1 (CM-1) is traditionally defined by tonsillar herniation, yet clinical symptoms often correlate poorly with simple linear measurements. Emerging research suggests that the geo...
Juan A Medina,Yamila Basilotta Marquez,Ramiro Del Rio et al. Juan A Medina et al.
Background: Intracranial malignant peripheral nerve sheath tumors (MPNSTs) are exceptionally rare, and primary origin from cranial nerves is particularly uncommon. Involvement of the oculomotor nerve represents an extraor...