نتایج جستجو برای: optic pathway glioma

تعداد نتایج: 389384  

2016
Nina Mikirova Ronald Hunnunghake Ruth C. Scimeca Charles Chinshaw Faryal Ali Chris Brannon Neil Riordan

BACKGROUND In neurofibromatosis type 1 (NF1) disease, the loss of the tumor suppressor function of the neurofibromin gene leads to proliferation of neural tumors. In children, the most frequently identified tumor is the optic pathway glioma. CASE REPORT We describe the case of a 5-year-old child who was diagnosed with NF1 and optic pathway tumor onset at the age of 14 months. Because of the tum...

Journal: :Journal of Korean Neurosurgical Society 2018

2017
Anne C Solga Joseph A Toonen Yuan Pan Patrick J Cimino Yu Ma Guillaume A Castillon Scott M Gianino Mark H Ellisman Da Yong Lee David H Gutmann

Low-grade gliomas are one of the most common brain tumors in children, where they frequently form within the optic pathway (optic pathway gliomas; OPGs). Since many OPGs occur in the context of the Neurofibromatosis Type 1 (NF1) cancer predisposition syndrome, we have previously employed Nf1 genetically-engineered mouse (GEM) strains to study the pathogenesis of these low-grade glial neoplasms....

2010
Jacquelyn A. Brown Scott M. Gianino David H. Gutmann

Individuals with the neurofibromatosis type 1 (NF1) inherited cancer syndrome exhibit neuronal dysfunction that predominantly affects the CNS. In this report, we demonstrate a unique vulnerability of CNS neurons, but not peripheral nervous system (PNS) neurons, to reduced Nf1 gene expression. Unlike dorsal root ganglion neurons, Nf1 heterozygous (Nf1 / ) hippocampal and retinal ganglion cell (R...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Jacquelyn A Brown Scott M Gianino David H Gutmann

Individuals with the neurofibromatosis type 1 (NF1) inherited cancer syndrome exhibit neuronal dysfunction that predominantly affects the CNS. In this report, we demonstrate a unique vulnerability of CNS neurons, but not peripheral nervous system (PNS) neurons, to reduced Nf1 gene expression. Unlike dorsal root ganglion neurons, Nf1 heterozygous (Nf1+/-) hippocampal and retinal ganglion cell (R...

Journal: :Neuro-oncology 2015
Aparna Kaul Joseph A Toonen Scott M Gianino David H Gutmann

BACKGROUND Children with the neurofibromatosis type 1 (NF1) tumor predisposition syndrome are prone to the development of optic pathway gliomas resulting from biallelic inactivation of the NF1 gene. Recent studies have revealed the presence of other molecular alterations in a small portion of these NF1-associated brain tumors. The purpose of this study was to leverage Nf1 genetically engineered...

2018
Patrick W. Hales Victoria Smith Deepi Dhanoa-Hayre Patricia O'Hare Kshitij Mankad Felice d'Arco Jessica Cooper Ramneek Kaur Kim Phipps Richard Bowman Darren Hargrave Christopher Clark

Background Radiological biomarkers which correlate with visual function are needed to improve the clinical management of optic pathway glioma (OPG) patients. Currently, these are not available using conventional magnetic resonance imaging (MRI) sequences. The aim of this study was to determine whether diffusion MRI could be used to delineate the entire optic pathway in OPG patients, and provide...

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