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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
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Journal Article
Histopathology, ISSN 0309-0167, 09/2018, Volume 73, Issue 3, pp. 483 - 491
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Journal Article
Journal Article
World Neurosurgery, ISSN 1878-8750, 2016, Volume 85, pp. 197 - 204
Background Atypical teratoid/rhabdoid tumors (AT/RTs) are highly malignant neoplasms that rarely occur in adults. Due to the complex histology of AT/RTs, the... 
Neurosurgery | Brain tumor | Rhabdoid tumor | Clinical management | Pineal tumor | Atypical teratoid/rhabdoid tumor | Genomics | SURGERY | MALIGNANT RHABDOID TUMOR | GLIOMA | ACTIN CYTOSKELETON ORGANIZATION | CLINICAL NEUROLOGY | GLIOBLASTOMA | PLEOMORPHIC XANTHOASTROCYTOMA | CENTRAL-NERVOUS-SYSTEM | OF-THE-LITERATURE | YOUNG-ADULT | A-CASE-REPORT | BRAIN | Pituitary Neoplasms - surgery | Pituitary Neoplasms - diagnosis | Humans | Middle Aged | Teratoma - diagnosis | Male | Rhabdoid Tumor - pathology | Teratoma - surgery | Chemoradiotherapy, Adjuvant | SMARCB1 Protein | DNA Mutational Analysis | Teratoma - radiotherapy | Diagnosis, Differential | Infratentorial Neoplasms - genetics | Rhabdoid Tumor - surgery | Infratentorial Neoplasms - radiotherapy | Pituitary Neoplasms - genetics | Gene Silencing | Rhabdoid Tumor - radiotherapy | Pituitary Neoplasms - pathology | Combined Modality Therapy | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Infratentorial Neoplasms - pathology | Chromosomal Proteins, Non-Histone - genetics | Magnetic Resonance Imaging | Teratoma - pathology | Neurologic Examination | Rhabdoid Tumor - genetics | Biopsy | Genetic Markers - genetics | Brain - pathology | Infratentorial Neoplasms - surgery | Teratoma - genetics | Brain - surgery | Rhabdoid Tumor - diagnosis | Infratentorial Neoplasms - diagnosis | Medical colleges | Adults | Tumors
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Journal Article
Acta Neuropathologica, ISSN 0001-6322, 5/2012, Volume 123, Issue 5, pp. 727 - 738
Journal Article
Journal Article
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