Results 61 to 70 of about 2,340 (196)

Studies with the Golgi method in central gangliogliomas and dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos disease) [PDF]

, 2017
The rapid Golgi method, combined with current optical and electronmicroscopica1 techniques, was used in three central gangliogliomas and in one dysplastic gangliocytoma of the cerebellum to study the morphology of ganglionic cells.
Bella, R., Conesa Bertrán, Gerardo, Ferrer, Isidro (Ferrer Abizanda), Guionnet, N., Isamat de la Riva, F. (Fabián), Martí, E., Serrano Piñol, M. Teresa, Towse, J.   +7 more
core  

cIMPACT‐NOW update 10: Recommendations for defining new types for central nervous system tumor classification

Brain Pathology, Volume 35, Issue 6, November 2025.
Cynthia Hawkins, Kenneth Aldape, David Capper, Andreas von Deimling, Caterina Giannini, Mark R. Gilbert, Thomas S. Jacques, David Jones, Takashi Komori, David N. Louis, Sabine Mueller, MacLean Nasrallah, Brent A. Orr, Arie Perry, Stefan M. Pfister, Felix Sahm, Chitra Sarkar, Matija Snuderl, David Solomon, Pascale Varlet, Pieter Wesseling, Guido Reifenberger   +21 more
wiley   +1 more source

A Novel Germline MUTYH Mutation (p.W156∗) in High‐Grade Astrocytoma, IDH Mutant

Human Mutation, Volume 2025, Issue 1, 2025.
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, Shaoyan Xi, Lei Yuan, Ziteng Li, Xiaoyun Liu, Jiamei Gu, Shuo Li, Liyun Huang, Wanming Hu, Lingyi Fu, Aziz ur Rehman Aziz   +10 more
wiley   +1 more source

The last decade\u27s experience of management of central neurocytomas: Treatment strategies and new options [PDF]

, 2021
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

Optic pathway gliomas in children: Clinical characteristics, treatment, and outcome of 95 patients in a single center over a 31‐year period. Can we avoid radiotherapy?

Pediatric Blood &Cancer, Volume 71, Issue 12, December 2024.
Abstract Background Optic pathway gliomas (OPG) are rare tumors in children. Lesion extent, visual functions, neurofibromatosis 1 (NF1), and age are factors that guide treatment. This study evaluates the clinical characteristics, treatment, and outcome of children and adolescents with OPG treated over a 31‐year period in a single center. Methods Ninety‐
Rejin Kebudi, Ulku Miray Yildirim, Ayça İribaş, Samuray Tuncer   +3 more
wiley   +1 more source

Central neurocytoma: report of two cases Neurocitoma central: relato de dois casos

Arquivos de Neuro-Psiquiatria, 2005
INTRODUCTION: Central neurocytomas are rare neuroectodermal tumors believed to arise from the subependymal matrix of the lateral ventricles. CASE REPORTS: A 26-year-old woman and a 33-year-old man each had a large, heterogeneous, contrast enhancing mass ...
Guilherme Borges, Hoyama Costa Pereira, Edmur Franco Carelli, Yvens Barbosa Fernandes, Leonardo Bonilha, Maria Fernanda Roma, Verônica A. Zanardi, José R. Menezes Netto, André A. Schenka, Luciano S. Queiroz   +9 more
doaj   +1 more source

Intraoperative Consultations of Central Nervous System Tumors: A Review for Practicing Pathologists and Testing of an Algorithmic Approach. [PDF]

, 2019
Intraoperative consultations or frozen sections for central nervous system (CNS) tumors present a significant challenge for surgical pathologists because of their relative rarity and diversity.
Ding, Cristine, Oran, Gülbin, Tihan, Tarık, Yüksek, Gül Emek, Çakir, Emel   +4 more
core  

Phenotypic and epigenetic heterogeneity in FGFR2‐fused glial and glioneuronal tumours

Neuropathology and Applied Neurobiology, Volume 50, Issue 6, December 2024.
FGFR2‐fused brain tumours might represent rather a spectrum of paediatric diffuse low‐grade glioma, glioneuronal and neuronal tumours overlapping PLNTY and ganglioglioma than a unique tumour type.Although the differences are very slight in terms of histopathology or epigenetics, neuroradiology identifies two distinct radiological patterns suggesting ...
Alice Métais, Volodia Dangouloff‐Ros, Jeremy Garcia, Quentin Vannod‐Michel, Marie Csanyi, Arnault Tauziède‐Espariat, Romain Appay, Claude‐Alain Maurage, Emmanuelle Uro‐Coste, David Meyronet, Valérie Rigau, Audrey Rousseau, Guillaume Chotard, Jocelyne Hamelin, Gaelle Pierron, Carole Colin, Morgan Ollivier, Margaux Roques, Corentin Provost, Jean‐Philippe Cottier, Johan Pallud, Fabrice Chrétien, Lelio Guida, Thomas Blauwblomme, Nathalie Boddaert, Pascale Varlet, Myriam Edjlali, Dominique Figarella‐Branger, contributors of the Biopathology RENOCLIP‐LOC network, of the Neuroradiological RENOCLIP‐LOC network   +29 more
wiley   +1 more source

Molecular and clinical characterization of atypical central neurocytomas: implications for diagnosis and treatment strategies

Discover Oncology
Objectives This study aimed to investigate the histological and molecular characteristics of atypical central neurocytomas (CNs) and evaluate their clinical treatment outcomes, with the aim of identifying reliable biomarkers for differentiation and ...
Feixia Sun, Zuocheng Yang, Ronghua Kong, Song Han   +3 more
doaj   +1 more source

Successful Treatment of MDR Acinetobacter baumannii Meningitis in a Young Adult Patient With Intraventricular and Intravenous Polymyxin B‐Tigecycline Based Combinations: A Case Report

Clinical Case Reports, Volume 12, Issue 11, November 2024.
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, Himel Kumar Biswas, Md Abdul Kader Zilani, Rama Biswas, Sirazul Haque Ershad   +4 more
wiley   +1 more source