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1. Full Text Rosette-Forming Glioneuronal Tumor of Spinal Cord
by Collin, Adrien and Adle-Biassette, Homa and Lecler, Augustin
World Neurosurgery, ISSN 1878-8750, 11/2018, Volume 119, pp. 242 - 243
Rosette-forming glioneuronal tumor has recently been included in the World Health Organization classification as a low-grade tumor. It usually occurs in young... 
Spinal | Rosette-forming glioneuronal tumor | Tumor | MRI | RGNT | SURGERY | CLINICAL NEUROLOGY | Spinal Cord Neoplasms - diagnostic imaging | Diagnosis, Differential | Glioma - diagnostic imaging | Glioma - pathology | Humans | Spinal Cord Neoplasms - surgery | Adult | Female | Spinal Cord Neoplasms - pathology | Glioma - surgery | Tumors
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2. Full Text Malignant Transformation of a Rosette-Forming Glioneuronal Tumor to Glioblastoma
by Kwon, Sae Min and Kim, Young-Hoon and Kim, Chang Jin and Kim, Jeong Hoon and Byun, Joonho and Hong, Seok Ho and Cho, Young Hyun
World Neurosurgery, ISSN 1878-8750, 10/2019, Volume 130, pp. 271 - 275
A rosette-forming glioneuronal tumor (RGNT), a rare brain tumor, presents as a benign feature with a favorable outcome. To date, a few cases with aggressive... 
Rosette-forming glioneuronal tumor | Malignant transformation | Glioblastoma | SURGERY | NERVOUS-SYSTEM | 4TH-VENTRICLE | PILOCYTIC ASTROCYTOMA | CLASSIFICATION | CLINICAL NEUROLOGY | FEATURES | Medical colleges | Glioblastoma multiforme | Brain tumors
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3. Full Text Comprehensive genetic characterization of rosette‐forming glioneuronal tumors: independent component analysis by tissue microdissection
by Kitamura, Yohei and Komori, Takashi and Shibuya, Makoto and Ohara, Kentaro and Saito, Yuko and Hayashi, Saeko and Sasaki, Aya and Nakagawa, Eiji and Tomio, Ryosuke and Kakita, Akiyoshi and Nakatsukasa, Masashi and Yoshida, Kazunari and Sasaki, Hikaru
Brain Pathology, ISSN 1015-6305, 01/2018, Volume 28, Issue 1, pp. 87 - 93
A rosette‐forming glioneuronal tumor (RGNT) is a rare mixed neuronal‐glial tumor characterized by biphasic architecture of glial and neurocytic components. The... 
mixed neuronal‐glial tumor | genetics | PIK3CA | CGH | FGFR1 | rosette‐forming glioneuronal tumor | rosette-forming glioneuronal tumor | mixed neuronal-glial tumor | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMORS | IDH1 | FGFR1 N546K | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | 4TH-VENTRICLE | MUTATIONS | PAPILLARY | KIAA1549-BRAF FUSION | ABERRATIONS | Neurons - pathology | Class I Phosphatidylinositol 3-Kinases - genetics | Class I Phosphatidylinositol 3-Kinases - metabolism | Microdissection | Neuroglia - pathology | Brain Neoplasms - diagnostic imaging | Humans | Middle Aged | Brain Neoplasms - pathology | Receptor, Fibroblast Growth Factor, Type 1 - metabolism | Male | Mutation, Missense | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Brain Neoplasms - metabolism | Glioma - metabolism | Glioma - genetics | Young Adult | Glioma - pathology | Adult | Female | Neurons - metabolism | Child | Tissue Preservation | Brain Neoplasms - genetics | Glioma - diagnostic imaging | Adolescent | Neuroglia - metabolism | Aged | Genetic research | Genetic aspects | Analysis | Tumors | Missense mutation | Independent component analysis | Forming | Chromosome 13 | Genetic diversity | Mutation | Fibroblast growth factor receptor 1 | Neuronal-glial interactions
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4. Full Text Glioneuronal tumours with features of rosette‐forming glioneuronal tumours of the fourth ventricle and dysembryoplastic neuroepithelial tumours: a report of three cases
by Chen, Shi‐Yun and Wang, Wei and Wang, Lei‐Ming and Lin, Qing‐Tang and Zhao, Guo‐Guang and Xu, Geng and Lu, De‐Hong and Piao, Yue‐Shan
Histopathology, ISSN 0309-0167, 02/2016, Volume 68, Issue 3, pp. 378 - 387
Aims To study three atypical glioneuronal tumours (GNTs), in order to shed light on the clinical and pathological features of this diverse tumour group.... 
dysembryoplastic neuroepithelial tumours | rosette‐forming glioneuronal tumours | glioneuronal tumours | molecular analysis | Molecular analysis | Glioneuronal tumours | Dysembryoplastic neuroepithelial tumours | Rosette-forming glioneuronal tumours | OLIGODENDROGLIOMA | FUSION | rosette-forming glioneuronal tumours | PRECURSOR CELL | NEURONAL DIFFERENTIATION | PATHOLOGY | CELL BIOLOGY | ASTROCYTE | PATIENT | EPILEPSY | SPECTRUM | Astrocytoma - genetics | Humans | Brain Neoplasms - pathology | Brain Neoplasms - genetics | Male | Basal Ganglia - pathology | Neoplasms, Neuroepithelial - pathology | Rosette Formation | Parietal Lobe - pathology | Glioma - genetics | Young Adult | Astrocytoma - pathology | Glioma - pathology | Adolescent | Neoplasms, Neuroepithelial - genetics | Adult | Female | Retrospective Studies | Fourth Ventricle - pathology | Analysis | Tumors
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5. Full Text Imaging features of rosette-forming glioneuronal tumours (RGNTs): A Series of seven cases
by Medhi, Gorky and Medhi, Gorky and Prasad, Chandrajit and Prasad, Chandrajit and Saini, Jitender and Saini, Jitender and Pendharkar, Hima and Pendharkar, Hima and Bhat, Maya Dattatraya and Bhat, Maya Dattatraya and Pandey, Paritosh and Pandey, Paritosh and Muthane, Yasha and Muthane, Yasha
European Radiology, ISSN 0938-7994, 1/2016, Volume 26, Issue 1, pp. 262 - 270
Rosette-forming glioneuronal tumours (RGNTs) are a recently described, rare, distinct nosological entity of the glioneuronal family. We describe imaging... 
Rosette forming glioneuronal tumour | Histopathology | Medicine & Public Health | Diagnostic Radiology | Imaging | CSF dissemination | Internal Medicine | Interventional Radiology | Imaging / Radiology | Haemorrhage | Ultrasound | Neuroradiology | NERVOUS-SYSTEM | 4TH-VENTRICLE | CLASSIFICATION | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Ganglioglioma - diagnosis | Humans | Spinal Cord - diagnostic imaging | Magnetic Resonance Imaging - methods | Tomography, X-Ray Computed - methods | Male | Cerebral Ventricle Neoplasms - diagnosis | Young Adult | Fourth Ventricle - diagnostic imaging | Spinal Cord - pathology | Adolescent | Adult | Female | Retrospective Studies | Fourth Ventricle - pathology | Child | Diagnostic imaging | Tumors
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6. Full Text SLC44A1 – PRKCA fusion in papillary and rosette-forming glioneuronal tumors
by Nagaishi, Masaya and Nobusawa, Sumihito and Matsumura, Nozomi and Kono, Fumihiko and Ishiuchi, Shogo and Abe, Tatsuya and Ebato, Michimasa and Wang, Yin and Hyodo, Akio and Yokoo, Hideaki and Nakazato, Yoichi
Journal of Clinical Neuroscience, ISSN 0967-5868, 2015, Volume 23, pp. 73 - 75
Abstract We investigated the fused protein of solute carrier family 44 choline transporter member 1 ( SLC44A1 ) and protein kinase C alpha ( PRKCA ) in three... 
Neurology | SLC44A–PRKCA fusion | Rosette-forming glioneuronal tumor | Papillary glioneuronal tumor | Fluorescence in situ hybridization | SLC44A-PRKCA fusion | 4TH-VENTRICLE | MUTATIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | Organic Cation Transport Proteins - metabolism | Protein Kinase C-alpha - metabolism | Brain Neoplasms - diagnosis | Humans | Protein Kinase C-alpha - genetics | Brain Neoplasms - genetics | In Situ Hybridization, Fluorescence | Male | Rosette Formation | Antigens, CD - genetics | Neoplasms, Neuroepithelial - metabolism | Brain Neoplasms - metabolism | Antigens, CD - metabolism | Neoplasms, Neuroepithelial - diagnosis | Neoplasms, Neuroepithelial - genetics | Biomarkers, Tumor - metabolism | Female | Biomarkers, Tumor - genetics | Organic Cation Transport Proteins - genetics | Tumors | Medical colleges | Chromosomes | Protein kinases
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7. Full Text An individual patient data meta-analysis on characteristics and outcome of patients with papillary glioneuronal tumor, rosette glioneuronal tumor with neuropil-like islands and rosette forming glioneuronal tumor of the fourth ventricle
by Schlamann, Annika and Von Bueren, André O and Hagel, Christian and Zwiener, Isabella and Seidel, Clemens and Kortmann, Rolf-Dieter and Müller, Klaus
PLoS ONE, ISSN 1932-6203, 07/2014, Volume 9, Issue 7, p. e101211
Background and Purpose: In 2007, the WHO classification of brain tumors was extended by three new entities of glioneuronal tumors: papillary glioneuronal tumor... 
ENTITY | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR | MULTIDISCIPLINARY SCIENCES | DISSEMINATION | SPINAL-CORD | CLASSIFICATION | CENTRAL-NERVOUS-SYSTEM | VARIANT | ADULT | FEATURES | Prognosis | Follow-Up Studies | Glioma - diagnosis | Humans | Middle Aged | Brain Neoplasms - pathology | Child, Preschool | Male | Neoplasms, Neuroepithelial - pathology | Young Adult | Neoplasms, Neuroepithelial - diagnosis | Glioma - pathology | Neoplasms, Neuroepithelial - mortality | Adult | Female | Brain Neoplasms - mortality | Child | Databases, Factual | Glioma - mortality | Brain Neoplasms - diagnosis | Kaplan-Meier Estimate | Proportional Hazards Models | Disease-Free Survival | Magnetic Resonance Imaging | Adolescent | Aged | Chemotherapy | Patient outcomes | Analysis | Tumors | Cancer | Brain | Pediatrics | Spinal cord | Data analysis | Neuropathology | Brain tumors | Brain cancer | Oncology | Ventricles (cerebral) | Forming | Data processing | Nervous system | Neuropil | Radiation therapy | Medical diagnosis | Patients | Survival | Meta-analysis | Survival analysis | Medical prognosis | Diagnostic systems | Ventricle | Islands
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8. Full Text Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1
by Sievers, Philipp and Appay, Romain and Schrimpf, Daniel and Stichel, Damian and Reuss, David E and Wefers, Annika K and Reinhardt, Annekathrin and Coras, Roland and Ruf, Viktoria C and Schmid, Simone and de Stricker, Karin and Boldt, Henning B and Kristensen, Bjarne Winther and Petersen, Jeanette Krogh and Ulhøi, Benedicte P and Gardberg, Maria and Aronica, Eleonora and Hasselblatt, Martin and Brück, Wolfgang and Bielle, Franck and Mokhtari, Karima and Lhermitte, Benoît and Wick, Wolfgang and Herold-Mende, Christel and Hänggi, Daniel and Brandner, Sebastian and Giangaspero, Felice and Capper, David and Rushing, Elisabeth and Wesseling, Pieter and Pfister, Stefan M and Figarella-Branger, Dominique and von Deimling, Aneas and Sahm, Felix and Jones, David T. W
Acta neuropathologica, ISSN 0001-6322, 2019, Volume 138, Issue 3, pp. 497 - 504
Rosette-forming glioneuronal tumor (RGNT) is a rare brain neoplasm that primarily affects young adults. Although alterations affecting the mitogen-activated... 
Neurosciences | Rosette-forming glioneuronal tumor | DNA methylation profile | MAPK | Brain tumor | Molecular classification | Pathology | Medicine & Public Health | PI3K | PIK3CA | NF1 | RGNT | FGFR1 | SYSTEM | FUSION | CLASSIFICATION | BRAF | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | 4TH-VENTRICLE | GENETIC ALTERATIONS | Epigenetic inheritance | Gliomas | Brain tumors | Genomics | DNA | Genetic aspects | Genomes | Methylation | Neurophysiology | Young adults | Therapeutic applications | MAP kinase | Kinases | 1-Phosphatidylinositol 3-kinase | Signal transduction | Protein kinase | DNA methylation | Tumor suppressor genes | Mutation | Fibroblast growth factor receptor 1 | Deoxyribonucleic acid--DNA | DNA sequencing | Tumors
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9. Full Text The expanding family of glioneuronal tumors
by Allende, Daniela S and Prayson, Richard A
Advances in Anatomic Pathology, ISSN 1072-4109, 01/2009, Volume 16, Issue 1, pp. 33 - 39
Three new entities have been recently added to the group of glioneuronal tumors in the most recent update of the World Health Organization classification of... 
Rosetted glioneuronal tumor with neuropil-like islands | Rosette-forming glioneuronal tumor of the fourth ventricle | Glioneuronal tumors | Papillary glioneuronal tumor | rosetted glioneuronal tumor with neuropil-like islands | NEUROPIL-LIKE ISLANDS | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR | glioneuronal tumors | 4TH-VENTRICLE | FOLLOW-UP | DIFFERENTIATION | PATHOLOGY | HISTOGENETIC IMPLICATIONS | papillary glioneuronal tumor | rosette-forming glioneuronal tumor of the fourth ventricle | GANGLIOGLIOMAS | Central Nervous System Neoplasms - classification | Neurons - pathology | Central Nervous System Neoplasms - pathology | Glioma - classification | Ganglioglioma - pathology | Glioma - pathology | Humans | Brain Neoplasms - pathology | Cell Differentiation | Cerebral Ventricle Neoplasms - pathology
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10. Rosette-forming and papillary glioneuronal tumors - A clinicopathological and molecular analysis
by Singh, V and Gupta, K and Salunke, P and Kumar, S and Radotra, BD and Vasishta, RK
CLINICAL NEUROPATHOLOGY, ISSN 0722-5091, 07/2019, Volume 38, Issue 4, pp. 180 - 188
Introduction: Rosette-forming glioneuronal tumors (RGNT) and papillary glioneuronal tumors (PGNT) account for < 1% of brain tumors. Genetic data regarding RGNT... 
PIK3CA MUTATIONS | GENE | glioneuronal tumors | glioneuronal tumor | 4TH-VENTRICLE | rosette-forming | PATHOLOGY | KIAA1549-BRAF FUSION | papillary glioneuronal tumor | CLINICAL NEUROLOGY
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11. Full Text Disseminated Rosette-Forming Glioneuronal Tumor with Spinal Drop Metastasis, a Uniquely Aggressive Presentation of Rare Tumor
by Silveira, Luke and DeWitt, John and Thomas, Alissa and Tranmer, Bruce
World Neurosurgery, ISSN 1878-8750, 12/2019, Volume 132, pp. 7 - 11
The rosette-forming glioneuronal tumor (RGNT) is a rare World Health Organization grade I tumor, most often originating in the fourth ventricle and... 
Spinal drop metastasis | Disseminated | Rosette-forming glioneuronal tumor (RGNT)
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12. Full Text Histopathological, molecular, clinical and radiological characterization of rosette-forming glioneuronal tumor in the central nervous system
by Yang, Chenlong and Fang, Jingyi and Li, Guang and Li, Shaowu and Ha, Tingting and Wang, Jiangfei and Yang, Bao and Yang, Jun and Xu, Yulun
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 65, pp. 109175 - 109190
Objective: A rosette-forming glioneuronal tumor (RGNT) is a rare entity originally described in the fourth ventricle. Recently, RGNTs occurring in... 
Brain tumor | Rosette-forming glioneuronal tumor | Spinal cord tumor | Treatment | Central nervous system | rosette-forming glioneuronal tumor | treatment | FUSION | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR | brain tumor | CLASSIFICATION | MUTISM | central nervous system | CELL BIOLOGY | 3RD-VENTRICLE | spinal cord tumor | IMAGING FEATURES | 4TH-VENTRICLE | PATIENT | MUTATIONS | NEUROFIBROMATOSIS TYPE-1
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13. Full Text Glioneuronal tumours with features of rosette-forming glioneuronal tumours of the fourth ventricle and dysembryoplastic neuroepithelial tumours: a report of three cases
by Chen, SY and Wang, W and Wang, LM and Lin, QT and Zhao, GG and Xu, G and Lu, DH and Piao, YS
HISTOPATHOLOGY, ISSN 0309-0167, 02/2016, Volume 68, Issue 3, pp. 378 - 387
Aims: To study three atypical glioneuronal tumours (GNTs), in order to shed light on the clinical and pathological features of this diverse tumour group.... 
dysembryoplastic neuroepithelial tumours | OLIGODENDROGLIOMA | FUSION | rosette-forming glioneuronal tumours | PRECURSOR CELL | NEURONAL DIFFERENTIATION | PATHOLOGY | CELL BIOLOGY | ASTROCYTE | PATIENT | EPILEPSY | SPECTRUM | glioneuronal tumours | molecular analysis
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14. Full Text Rosette-Forming Glioneuronal Tumor in Opticochiasmatic Region—Novel Entity in New Location
by Sekar, Arunkumar and Rudrappa, Satish and Gopal, Swaroop and Ghosal, Nandita and Rai, Abhishek
World Neurosurgery, ISSN 1878-8750, 05/2019, Volume 125, pp. 253 - 256
Rosette-forming glioneuronal tumour [RGNT] is a relatively rare entity first identified as a separate entity in 2002. We are reporting the second case of RGNT... 
Rosette-forming glioneuronal tumor | Diagnosis | Management | Opticochiasmatic region | SURGERY | NOONAN SYNDROME | 4TH-VENTRICLE | PATIENT | CLINICAL NEUROLOGY
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15. Full Text Absence of KIAA1549-BRAF fusion in rosette-forming glioneuronal tumors of the fourth ventricle (RGNT)
by Gessi, Marco and Lambert, Sally R and Lauriola, Libero and Waha, Andreas and Collins, V Peter and Pietsch, Torsten
Journal of Neuro-Oncology, ISSN 0167-594X, 10/2012, Volume 110, Issue 1, pp. 21 - 25
Rosette-forming glioneuronal tumors (RGNT) of the fourth ventricle are rare mixed glioneuronal tumors included in the revised WHO classification of central... 
Cerebellum | Neurology | KIAA1549 | Medicine & Public Health | Rosette-forming glioneuronal tumors | FISH | Oncology | BRAF | Pilocytic astrocytomas | ONCOLOGY | PATHWAY | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR | PILOCYTIC ASTROCYTOMA | MUTATIONS | CLINICAL NEUROLOGY | Immunohistochemistry | Humans | Middle Aged | Brain Neoplasms - pathology | Brain Neoplasms - genetics | In Situ Hybridization, Fluorescence | Male | Rosette Formation | Ganglioglioma - genetics | Oncogene Proteins, Fusion - genetics | Proto-Oncogene Proteins B-raf - genetics | Ganglioglioma - pathology | Adolescent | Adult | Female | Oncogene Fusion - genetics | Fourth Ventricle - pathology | Child | Cerebral Ventricle Neoplasms - genetics | Interphase | Central nervous system | Classification | Data processing | Ventricles (cerebral) | Mutation | Astrocytoma | Gene fusion | Tumors
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16. Full Text An epilepsy‐associated glioneuronal tumor with mixed morphology harboring FGFR1 mutation
by Yamada, Seiji and Nobusawa, Sumihito and Yamazaki, Tatsuya and Teranishi, Takao and Watanabe, Sadayoshi and Murayama, Kazuhiro and Ohba, Shigeo and Okabe, Asako and Sakurai, Kouhei and Urano, Makoto and Tsukamoto, Tetsuya and Yokoo, Hideaki and Hirose, Yuichi and Abe, Masato
Pathology International, ISSN 1320-5463, 06/2019, Volume 69, Issue 6, pp. 372 - 377
Glioneuronal tumor (GNT) is a rare central nervous system neoplasm composed of glial and neuronal components. Making the specific diagnosis of GNT can be... 
glioneuronal tumor | dysembryoplastic neuroepithelial tumor | low‐grade epilepsy‐associated neuroepithelial tumors | pilocytic astrocytoma | FGFR1 | rosette‐forming glioneuronal tumor | rosette-forming glioneuronal tumor | low-grade epilepsy-associated neuroepithelial tumors | FORM | 4TH-VENTRICLE | PATHOLOGY | GENETIC ALTERATIONS | Epilepsy | Genetic aspects | Tumors | Temporal lobe | Leukocytes (eosinophilic) | Central nervous system | Case reports | Fluorescence | Gadolinium | Hybridization | Neuronal-glial interactions | Necrosis | Fibers | Cores | Missense mutation | Magnetic resonance imaging | Morphology | Fluorescence in situ hybridization | Hybridization analysis | Mutation | Fibroblast growth factor receptor 1 | Astrocytoma | Seizures
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17. Full Text Molecular profiling of a rare rosette-forming glioneuronal tumor arising in the spinal cord
by Bidinotto, Lucas Tadeu and Scapulatempo-Neto, Cristovam and Mackay, Alan and De Almeida, Gisele Caravina and Scheithauer, Bernd Walter and Berardinelli, Gustavo Noriz and Torrieri, Raul and Clara, Carlos Afonso and Feltrin, Leonir Terezinha and Viana-Pereira, Marta and Varella-Garcia, Marileila and Jones, Chris and Reis, Rui Manuel
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, p. e0137690
Rosette-forming glioneuronal tumor (RGNT) of the IV ventricle is a rare and recently recognized brain tumor entity. It is histologically composed by two... 
VENTRICLE | PILOCYTIC ASTROCYTOMAS | PATHWAY | MULTIDISCIPLINARY SCIENCES | PATIENT | MUTATIONS | KIAA1549-BRAF FUSION | MEDULLOBLASTOMA | EXPRESSION | 4TH-VENTRICLE RGNT | FEATURES | Chromosome Deletion | Magnetic Resonance Imaging | Exome - genetics | Spinal Cord | Brain Neoplasms - diagnosis | Humans | Brain Neoplasms - pathology | Brain Neoplasms - genetics | Adult | Male | Brain Neoplasms - metabolism | Gene mutations | Physiological aspects | Research | Immunohistochemistry | Brain | Health sciences | Pediatrics | Spinal cord | Profiling | Laboratories | Neuropathology | Brain tumors | Brain cancer | Oncology | Ventricles (cerebral) | Genomes | Neuronal-glial interactions | DNA methylation | Sodium channels (voltage-gated) | Chromosomes | Astrocytoma | Deoxyribonucleic acid--DNA | Medical research | Sequences | Genomic analysis | Chromosome 7 | MAP kinase | Forming | RNA polymerase | Gene expression | Gene fusion | Polymerase chain reaction | Amplification | Pathology | Hospitals | Mutation | Ventricle | Cancer | Tumors | Deoxyribonucleic acid | DNA
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18. Full Text A comprehensive analysis of 41 patients with rosette-forming glioneuronal tumors of the fourth ventricle
by Zhang, Joanne and Babu, Ranjith and McLendon, Roger E and Friedman, Allan H and Adamson, Cory
Journal of Clinical Neuroscience, ISSN 0967-5868, 2012, Volume 20, Issue 3, pp. 335 - 341
Abstract The rosette-forming glioneuronal tumor (RGNT) of the fourth ventricle is a recently described, rare, and distinct tumor of the glioneuronal family.... 
Neurology | Fourth ventricle | Rosette-forming glioneuronal tumor | Treatment | DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR | IDH1 | NEUROSCIENCES | CLINICAL NEUROLOGY | Young Adult | Ganglioglioma - therapy | Ganglioglioma - pathology | Humans | Middle Aged | Male | Cerebral Ventricle Neoplasms - pathology | Rosette Formation | Cerebral Ventricle Neoplasms - therapy | Fourth Ventricle - pathology | Tumors
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19. Full Text A Multifocal Glioneuronal Tumor with RGNT-Like Morphology Occupying the Supratentorial Ventricular System and Infiltrating the Brain Parenchyma
by Morassi, Mauro and Vivaldi, Oscar and Cobelli, Milena and Liserre, Barbara and Zorzi, Fausto and Bnà, Claudio
World Neurosurgery, ISSN 1878-8750, 01/2020, Volume 133, pp. 196 - 200
Rosette-forming glioneuronal tumors (RGNTs) with multifocal growth throughout the ventricular system are extremely rare, and only 1 case of RGNT with... 
Intraventricular glioneuronal tumors | Perfusion-weighted imaging | Tumor contrast enhancement variability | Rosette forming glioneuronal tumor
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