Results 71 to 80 of about 28,018 (244)

A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups

open access: yesPediatric Blood & Cancer, 2020
Relapse occurs in 50% of pediatric ependymoma cases and has poor prognosis. Few studies have investigated the clinical progress of relapsed disease, and treatment lacks a standardized approach.
Timothy A. Ritzmann   +9 more
semanticscholar   +1 more source

Spinal ependymoma SEER data

open access: yes, 2018
To identify the factors influencing survival of spinal ependymoma, we compiled spinal ependymoma cases diagnosed between 1973 and 2014 from the Surveillance, Epidemiology, and End Results (SEER ...
Ryu, S (via Mendeley Data)
core   +1 more source

Classification and neuroimaging of ependymal tumors

open access: yesFrontiers in Pediatrics, 2023
Ependymal tumors arise from the ependymal cell remnants of the cerebral ventricles, the central canal of the spinal cord, or the filum terminale or conus medullaris, although most pediatric supratentorial ependymomas do not exhibit clear communication or
Weiya Mu, Hisham Dahmoush
doaj   +1 more source

Nucleoporin TPR (translocated promoter region, nuclear basket protein) upregulation alters MTOR-HSF1 trails and suppresses autophagy induction in ependymoma

open access: yesAutophagy, 2020
Children with ependymoma have high mortality rates because ependymoma is resistant to conventional therapy. Genomic and transcriptomic studies have identified potential targets as significantly altered genes in ependymoma patients.
F. Dewi   +8 more
semanticscholar   +1 more source

Rapid spontaneous malignant progression of supratentorial tanycytic ependymoma with sarcomatous features - "Ependymosarcoma"

open access: yes, 2010
By analogy to gliosarcoma, the term "ependymosarcoma" has recently been coined to thematize the rare phenomenon of a malignant mesenchymal component arising within an ependymoma. We report on an example of this paradigm, involving tanycytic ependymoma as
Mariani, Luigi   +5 more
core   +1 more source

Cerebellar Clear Cell Ependymoma in a 10-Year-Old Girl

open access: yes대한영상의학회지, 2016
Clear cell ependymoma (CCE) is a histological rare variant (1–5%) of ependymoma, which is distinguished from other histological subtypes by the presence of fusiform cells arrayed radially around small blood vessels.
Aye Nyein Thinzar   +8 more
doaj   +1 more source

The Multifaceted Appearance of Supratentorial Ependymoma with ZFTA-MAML2 Fusion

open access: yesFree Neuropathology, 2021
Ependymomas are glial neoplasms with a wide morphological spectrum. The majority of supratentorial ependymomas are known to harbor ZFTA fusions, most commonly to RELA.
Ming Liang Oon   +8 more
doaj   +1 more source

YAP1/TAZ drives ependymoma-like tumour formation in mice

open access: yesNature Communications, 2020
YAP1 gene fusions have been observed in a subset of paediatric ependymomas. Here we show that, ectopic expression of active nuclear YAP1 (nlsYAP5SA) in ventricular zone neural progenitor cells using conditionally-induced NEX/NeuroD6-Cre is sufficient to ...
Noreen Eder   +14 more
semanticscholar   +1 more source

Isolated extracranial recurrence of anaplastic ependymoma

open access: yes, 2011
Anaplastic ependymoma is a malignant glial tumor thought to arise from radial glial cells of the ventricular zone. Because ependymoma is frequently encountered within ventricular spaces, they are prone to leptomeningeal dissemination.
Myseros, John S., MD   +3 more
core   +1 more source

Adjunctive treatment of myxopapillary ependymoma [PDF]

open access: yes, 2021
Myxopapillary ependymoma are rare tumors and optimal therapeutic strategy is remained controversial. The main treatments for myxopapillary ependymoma tumors include surgery and radiotherapy.
Najafi, M.   +6 more
core  

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