Results 31 to 40 of about 31,605 (321)

Molecular Characterization of Medulloblastoma in a Patient with Neurofibromatosis Type 1: Case Report and Literature Review

open access: yesDiagnostics, 2021
Brain tumors are the most common solid neoplasms of childhood. They are frequently reported in children with Neurofibromatosis type 1 (NF1). The most frequent central nervous system malignancies described in NF1 are optic pathway gliomas and brainstem ...
Marco Ranalli   +16 more
doaj   +1 more source

MicroRNA expression profiles in pediatric dysembryoplastic neuroepithelial tumors. [PDF]

open access: yes, 2016
© Springer Science+Business Media New York 2015Among noncoding RNAs, microRNAs (miRNAs) have been most extensively studied, and their biology has repeatedly been proven critical for central nervous system pathological conditions.
A Ranger   +36 more
core   +2 more sources

E-survey of current international physiotherapy practice for children with ataxia following surgical resection of posterior fossa tumour. [PDF]

open access: yes, 2018
ObjectiveTo determine current international practice regarding physiotherapy input for children with ataxia following surgery for posterior fossa tumour.
Bunn, Lisa   +6 more
core   +7 more sources

The Prognostic and Predictive Significance of circRNA CDR1as in Tumor Progression

open access: yesFrontiers in Oncology, 2021
Cerebellar degeneration-related protein 1 antisense (CDR1as) is an important member of the circRNAs family, also known as cirs-7. Its main function in vivo is to act as a mir-7 sponge.
Fang Jian   +8 more
doaj   +1 more source

A Case of Congenital Brainstem Oligodendroglioma: Pathology Findings and Review of the Literature

open access: yesCase Reports in Neurological Medicine, 2017
Congenital and perinatal primary brain neoplasms are extremely rare. Brainstem neoplasms in the perinatal and neonatal period are typically of high-grade nature and have poor prognoses with survival rates of less than 2 years from diagnosis.
Stefan Kostadinov, Suzanne de la Monte
doaj   +1 more source

Embryonal tumor with multilayered rosettes in a teenager

open access: yesAutopsy and Case Reports, 2022
Background: Embryonal tumor with multilayered rosettes (ETMR), NOS/C19MC- altered, is a rare and recently classified highly aggressive malignant brain tumor in the 2021 World Health Organization (WHO) classification of tumors of the central nervous ...
Kofi Ulzen-Appiah   +1 more
doaj  

Unique Finding of a Primary Central Nervous System Neuroendocrine Carcinoma in a 5-Year-Old Child: A Case Report

open access: yesFrontiers in Neuroscience, 2022
Neuroendocrine tumors (NETs) are rare neoplasms predominantly arising in the gastrointestinal-tract or the lungs of adults. To date, only ten cases of primary central nervous system (CNS) NETs have been reported, with just three of them describing a ...
Natalia Stepien   +15 more
doaj   +1 more source

Glioblastoma Multiforme in the Posterior Cranial Fossa in a Patient with Neurofibromatosis Type I

open access: yesCase Reports in Medicine, 2009
Patients with Neurofibromatosis type 1 (NF1) have an increased risk of developing neoplasms. The most common brain tumors, found in 15%–20% of NF1 patients, are hypothalamic-optic gliomas, followed by brainstem and cerebellar pilocytic astrocytomas ...
Marike L. D. Broekman   +4 more
doaj   +1 more source

Extended retrosigmoid approach to ventro-lateral foramen magnum neuroenteric cyst: 2D- dimensional video

open access: yesInterdisciplinary Neurosurgery, 2023
Neuroenteric cysts (NC) are rare benign congenital neoplasms arising from displaced elements of the alimentary canal. They are commonly located within the spine.
Dan Zimelewicz Oberman   +1 more
doaj   +1 more source

Primary cerebellopontine angle melanocytoma: review. [PDF]

open access: yes, 2012
Introduction Primary cerebellopontine angle melanocytomas (PCPAMs) are very rare. Their natural history and prognosis are not fully understood. We reviewed the literature and add a new case to analyze PCPAM's presentation, radiological features, and ...
Elashaal, R   +3 more
core   +1 more source

Home - About - Disclaimer - Privacy