Results 41 to 50 of about 984 (179)
The last decade\u27s experience of management of central neurocytomas: Treatment strategies and new options [PDF]
Background: The purpose of the presented work is to evaluate the last decade\u27s experience in surgical management of central neurocytoma (CN) and elucidate on the treatment strategies and new options.
Siomin, Vitaly
core +1 more source
Rosette-forming glioneuronal tumor: a pineal region case with IDH1 and IDH2 mutation analyses and literature review of 43 cases [PDF]
Rosette-forming glioneuronal tumor (RGNT) of the fourth ventricle is a mixed glio-neuronal neoplasm recently codified by the World Health Organization WHO Classification of Central Nervous System (CNS) Tumors (2007). To date, 43 cases have been described
Orestes E. Solis +10 more
core +2 more sources
The 2021 WHO Classification of Tumors of the Central Nervous System: a summary [PDF]
The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, is the sixth version of the international standard for the classification of brain and spinal cord tumors.
Brat, Daniel J +12 more
core +3 more sources
학위논문(박사) -- 서울대학교대학원 : 의과대학 의학과, 2022. 8. 박철기.배경: 중심성 신경세포종은 일반적으로 젊은 성인에게서 많이 발생하는 중추신경계에서 가장 드물게 발생하는 종양 중 하나이다. 중심성 신경세포종의 발생과 분화에 관련하여 통합적인 분자 및 유전자 특성 연구는 현재까지 부재하며 종양발생기전은 확실하게 밝혀지지 않았다.
탐린
core
Multi‐technology interventions (non‐invasive neuromodulation, AI, 3D organoids) for CNS tumor treatment shift from monotherapy to functional reconstruction. They address BBB restriction, tumor heterogeneity, and immune suppression via biological–psychological–technological convergence, enabling precision oncology through dynamic monitoring and ...
Junda Lai +5 more
wiley +1 more source
Diffuse Glioneuronal tumour with Oligodendroglioma‐like features and Nuclear Clusters (DGONC) – a molecularly‐defined glioneuronal CNS tumour class displaying recurrent monosomy 14 [PDF]
Aims: DNA methylation-based central nervous system (CNS) tumour classification has identified numerous molecularly distinct tumour types, and clinically relevant subgroups among known CNS tumour entities that were previously thought to represent ...
Aronica, E. +38 more
core +3 more sources
Posterior pituitary tumors and other rare entities involving the pituitary gland
Abstract Non‐neuroendocrine tumors account for around 10% of all primary neoplasms of the sella. If meningiomas, craniopharyngiomas, and germ cell tumors are excluded, the remaining lesions include a broad spectrum of uncommon, benign, and aggressive, often diagnostically challenging lesions.
Federico Roncaroli, Caterina Giannini
wiley +1 more source
Exploring the interdependencies of research funders in the UK [PDF]
Investment in medical research is vital to the continuing improvement of the UK's health and wealth. It is through research that we expand our understanding of disease and develop new treatments for patients.
Crane, P +13 more
core +1 more source
A Novel Germline MUTYH Mutation (p.W156∗) in High‐Grade Astrocytoma, IDH Mutant
Germline mutations in the DNA repair gene E. coli MutY homolog (MUTYH) are established predisposing factors for colorectal polyposis, colorectal carcinoma, and various extracolonic malignancies. Nevertheless, the association between MUTYH mutations and central nervous system (CNS) tumorigenesis remains poorly characterized.
Lulu Zhang +10 more
wiley +1 more source
ABSTRACT Multiple drug resistance to Acinetobacter baumannii infection treatment is a great challenge for neuro‐intensivists due to poor drug penetration through the blood–brain barrier (BBB). Fortunately, the intraventricular administration of polymyxin‐B and tigecycline seems to be effective; there are few case reports demonstrating the effectiveness
Md Abdur Rahim +4 more
wiley +1 more source

