Results 61 to 70 of about 7,310 (199)
A developmental and genetic classification for malformations of cortical development: update 2012. [PDF]
, 2012 Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopmental delay and epilepsy. In addition, study of these disorders contributes greatly to the understanding of normal brain
Barkovich, A James +4 more
core +3 more sources
Structural Fiber Tract Alterations in Relation to Surgery in Children With a Posterior Fossa Tumor
NMR in Biomedicine, Volume 39, Issue 4, April 2026.Children that undergo posterior fossa tumor resection may experience post‐surgery neurological symptoms related to disruption of the dentato‐rubro‐thalamic tract (DRTT). By comparing pre‐ and intraoperative diffusion MRI tractography, we observed more variation in microstructural measures in the DRTT near the resection cavity, which were more ...
Pien E. J. Jellema +7 more
wiley +1 more source
A case report of rare location of ganglioglioma
Egyptian Journal of Neurosurgery, 2019 Background Gangliogliomas are rare tumors of the central nervous system. They can occur anywhere in the central nervous system but are most commonly located in the temporal lobe and are mainly found in children.
Vikas Sharma +3 more
doaj +1 more source
Vestibular seizures and spontaneous downbeat nystagmus of ganglioglioma origin: a case report
BMC Neurology, 2023 Background Low-grade gangliogliomas (GGs) are typically epileptogenic intracranial neoplasms. Yet, the presentation of simplex vertiginous experience and spontaneous downbeat nystagmus (DBN) has not been reported to date. Case presentation We present the
Ruizhe Yang, Haiyan Wu, Zhiqiang Gao
doaj +1 more source
International Journal of Cancer, Volume 158, Issue 5, Page 1250-1261, 1 March 2026.What's New? Eloquent intracranial tumors present unique challenges in neurosurgical treatment due to their proximity to critical functional areas of the brain. This prospective, single‐center cohort study quantified real‐time changes in patients' subjective burden of health impairments using the Time Trade‐Off and Standard Gamble methods, providing ...
Lisa S. Hönikl +4 more
wiley +1 more source
Prospective multicentre evaluation and refinement of an analysis tool for magnetic resonance spectroscopy of childhood cerebellar tumours [PDF]
, 2018 BackgroundA tool for diagnosing childhood cerebellar tumours using magnetic resonance (MR) spectroscopy peak height measurement has been developed based on retrospective analysis of single-centre data.ObjectiveTo determine the diagnostic accuracy of the ...
Arvanitis, Theodoros N. +15 more
core +3 more sources
The epileptologist's perspective of focal cortical dysplasia type 3: From concept to management
Epilepsia, Volume 67, Issue 3, Page 1017-1031, March 2026.Abstract The recent International League Against Epilepsy (ILAE) official and updated classification of focal cortical dysplasia (FCD) includes a third type—FCD type 3—characterized by architectural abnormalities (cortical dyslamination) associated with another “principal” lesion: hippocampal sclerosis (HS), developmental tumors, vascular malformations,
André Palmini +10 more
wiley +1 more source
Arquivos de Neuro-Psiquiatria, 2006 METHOD: Forty-two patients with low-grade brain tumor and refractory epilepsy were studied. The mean age was 22.3 years. They were divided into two groups: Group A, patients with ganglioglioma (n=19) and group B, patients with other low-grade tumors (n ...
Paulo Thadeu Brainer-Lima +2 more
doaj +1 more source
PATH-38. ROSETTE-FORMING GLIONEURONAL TUMOR IS DEFINED BY FGFR1 ACTIVATING ALTERATIONS WITH FREQUENT ACCOMPANYING PI3K AND MAPK PATHWAY MUTATIONS [PDF]
, 2019 BACKGROUND Rosette-forming glioneuronal tumor (RGNT) is an uncommon CNS tumor originally described in the fourth ventricle characterized by a low-grade glial neoplasm admixed with a rosette-forming neurocytic component.
Aghi, Manish +49 more
core
, 2007 Sotos syndrome is an overgrowth condition characterized by cardinal features including excessive growth during childhood, macrocephaly, distinctive facial gestalt and various degrees of learning difficulty, and associated with variable minor features ...
Cormier-Daire Valérie +1 more
core +2 more sources