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期刊名:Neurooncology advances

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e-ISSN:2632-2498

IF/分区:4.6/Q1

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共收录本刊相关文章索引1413
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
Xiaoci Rong,Nan Chen,Yanghao Hou et al. Xiaoci Rong et al.
Pilocytic astrocytoma (PA) is a benign tumor with a low risk of high-grade transformation. High-grade astrocytoma with piloid features (HGAP) is a recently recognized tumor entity that may arise de novo or from low-grade gliomas. Here, we r...
Anders Overby Sjøstrøm,Maria Camilla Mathiasen,Ulrik Lassen et al. Anders Overby Sjøstrøm et al.
Glioblastoma (GBM) patients often face cognitive impairment, which may limit their capacity to comprehend complex trial information, particularly regarding genomic analyses and incidental findings. We analyzed consent forms from a genomic s...
Maged T Ghoche,Kenji Miki,Fanen Yuan et al. Maged T Ghoche et al.
Background: Adult IDH-mutant brainstem gliomas (BSGs) are rare and appear molecularly distinct from H3K27-altered diffuse midline gliomas. We aimed to provide a comprehensive characterization by integrating an institution...
Sahin Hanalioglu,Efecan Cekic,Emin Tabipoglu et al. Sahin Hanalioglu et al.
Background: Ischemic complications remain a significant risk indicator of morbidity after meningioma surgery. While tumor size and extent of resection (EOR) are recognized risk factors, the prognostic impact of peritumora...
Joshua Zhu,Maria Tsoli,Jean Bertoldo et al. Joshua Zhu et al.
Diffuse midline glioma (DMG) is an aggressive pediatric brain tumor with a 1%-2% overall survival, largely due to the ineffectiveness of conventional treatments such as chemotherapy and radiotherapy, as well as the inoperability of the tumo...
Sébastien Perreault,François Doz Sébastien Perreault
The NTRK1, NTRK2, and NTRK3 genes encode the TRKA, TRKB, and TRKC receptors, critical for nervous system development. Gene fusions involving neurotrophic tyrosine receptor kinase (NTRK) are found in various cancers. In the pediatric populat...
Chelsea Kotch,Peter de Blank,Jason Fangusaro et al. Chelsea Kotch et al.
Neurofibromatosis type 1 (NF1)-associated tumors typically develop in the setting of biallelic inactivation of the NF1 gene and resultant overactivation of the Ras/mitogen-activated protein kinase signaling pathway. Mitogen-activated protei...
Anna Mullins,Julie Bennett,Kee Kiat Yeo et al. Anna Mullins et al.
Adolescents and young adults (AYA: ages 15-39 years) are a unique population at risk of both pediatric-type and adult-type central nervous system (CNS) tumors. Targeted therapies are now available for a growing subset of CNS tumors represen...
Anfal Jasem M Alshammari,Darren Hargrave,Anirban Das Anfal Jasem M Alshammari
Unresectable pediatric low-grade glioma is a chronic disease that can cause significant morbidity in young patients. Historically, treatment has mainly involved chemotherapy, with many patients needing multiple lines of treatment for a recu...