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Critical Reviews in Oncology and Hematology, ISSN 1040-8428, 2007, Volume 63, Issue 1, pp. 81 - 89
Abstract Ependymomas are rare tumours of neuroectodermal origin classified as myxopapillary ependymoma and subependymoma (grade I), ependymoma (grade II) and... 
Hematology, Oncology and Palliative Medicine | Ependymomas | Treatment | Prognosis | treatment | MOLECULAR-GENETIC ANALYSIS | PROGNOSTIC-FACTORS | POSTERIOR-FOSSA EPENDYMOMAS | SPINAL-CORD EPENDYMOMAS | MALIGNANT BRAIN-TUMORS | CHOROID-PLEXUS TUMORS | prognosis | ependymomas | RADIATION-THERAPY | ONCOLOGY | NERVOUS-SYSTEM TUMORS | CHILDRENS CANCER GROUP | HEMATOLOGY | INTRACRANIAL EPENDYMOMA | Ependymoma - etiology | Age Distribution | Brain Neoplasms - etiology | Humans | Brain Neoplasms - pathology | Male | Spinal Cord Neoplasms - metabolism | Glial Fibrillary Acidic Protein - metabolism | Brain Neoplasms - metabolism | Brain Neoplasms - surgery | Incidence | Infratentorial Neoplasms - metabolism | Ependymoma - diagnosis | Infratentorial Neoplasms - epidemiology | Infratentorial Neoplasms - etiology | Spinal Cord Neoplasms - surgery | Ependymoma - pathology | Female | Spinal Cord Neoplasms - radiotherapy | Brain Neoplasms - radiotherapy | Ependymoma - epidemiology | Infratentorial Neoplasms - radiotherapy | Brain Neoplasms - diagnosis | Risk Factors | Neoplasm Recurrence, Local | Spinal Cord Neoplasms - etiology | Infratentorial Neoplasms - pathology | Ependymoma - metabolism | Ependymoma - surgery | Sex Factors | Spinal Cord Neoplasms - diagnosis | Survival Analysis | Infratentorial Neoplasms - surgery | Spinal Cord Neoplasms - pathology | Neoplasm Staging | Ependymoma - radiotherapy | Infratentorial Neoplasms - diagnosis | Brain Neoplasms - epidemiology | Spinal Cord Neoplasms - epidemiology | Chemotherapy | Cancer | Tumors
Journal Article
Journal of Neurosurgery, ISSN 0022-3085, 01/2003, Volume 98, Issue 1, pp. 82 - 94
Journal Article
Acta Neurochirurgica, ISSN 0001-6268, 9/2017, Volume 159, Issue 9, pp. 1603 - 1611
Pediatric hemangioblastomas are rare, and the clinical features, timing of surgical intervention, optimal treatment, and clinical outcomes are still unclear.We... 
Neurology | Von Hippel–Lindau disease | Surgical Orthopedics | Medicine & Public Health | Outcome | Minimally Invasive Surgery | Neurosurgery | Interventional Radiology | Management | Pediatric | Neuroradiology | Hemangioblastoma | SURGERY | BRAIN-STEM HEMANGIOBLASTOMAS | RESECTION | HYDROCEPHALUS | HIPPEL-LINDAU-DISEASE | POSTERIOR-FOSSA-TUMORS | SURGICAL-MANAGEMENT | RADIOSURGERY | CEREBELLAR HEMANGIOBLASTOMAS | NATURAL-HISTORY | CLINICAL NEUROLOGY | Von Hippel-Lindau disease | SINGLE-INSTITUTION | Hemangioblastoma - surgery | Prognosis | Follow-Up Studies | Hemangioblastoma - etiology | Humans | Cerebellar Neoplasms - etiology | Central Nervous System Neoplasms - surgery | Child, Preschool | Infant | Male | von Hippel-Lindau Disease - complications | Central Nervous System Neoplasms - etiology | China | Spinal Cord Neoplasms - surgery | Female | Retrospective Studies | Child | Brain Stem Neoplasms - etiology | Hydrocephalus - etiology | Spinal Cord Neoplasms - etiology | Disease Progression | Cysts - complications | Magnetic Resonance Imaging | Adolescent | Brain Stem Neoplasms - surgery | Cerebellar Neoplasms - surgery | Cerebellum | Intervention | Pediatrics | Spinal cord | Hydrocephalus | Brain stem | Central nervous system | Medical records | Intracranial pressure | Males | Patients | Cysts | Surgery | VHL protein | Children | Females | Tumors
Journal Article
Journal Article
Neuro-Oncology, ISSN 1522-8517, 9/2011, Volume 13, Issue 9, pp. 1030 - 1036
Journal Article