Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study - Wikidata - awgldk - TriplyDB

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

http://www.wikidata.org/entity/Q35800546

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Significance and therapeutic value of miRNAs in embryonal neural tumors Temozolomide in children with progressive low-grade glioma.Clinical, radiological, histological and molecular characteristics of paediatric epithelioid glioblastoma Atypical teratoid/rhabdoid tumor in sellar turcica in an adult: A case report and review of the literature.Activating mutations in BRAF characterize a spectrum of pediatric low-grade gliomas.Loss of INI1 expression defines a unique subset of pediatric undifferentiated soft tissue sarcomas.Atypical teratoid/rhabdoid tumors in adults: a case report and treatment-focused review Primary atypical teratoid/rhabdoid tumor of the optic nerve: a rare entity in an exceptional location.Composite pleomorphic xanthoastrocytoma-epithelioid glioneuronal tumor with BRAF V600E mutation - report of three cases The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation.Biology and Treatment of Rhabdoid Tumor.Molecular Transition of an Adult Low-Grade Brain Tumor to an Atypical Teratoid/Rhabdoid Tumor Over a Time-Course of 14 Years.Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma.Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumors.Pediatric rhabdoid tumors of kidney and brain show many differences in gene expression but share dysregulation of cell cycle and epigenetic effector genes.Atypical teratoid/rhabdoid tumor arising in the setting of a pleomorphic xanthoastrocytoma.Atypical teratoid/rhabdoid tumor arising in a malignant glioma.Development of an Atypical Teratoid Rhabdoid Tumor in a Meningioma.Atypical Teratoid/Rhabdoid Tumor (AT/RT) Arising From Ependymoma: A Type of AT/RT Secondarily Developing From Other Primary Central Nervous System Tumors.Rapid progression of rhabdoid components of a composite high-grade glioma and rhabdoid tumor in the occipital lobe of an adult.Optic pathway ganglioglioma with intraventricular cyst.

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P2860

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

http://www.wikidata.org/entity/Q35800546

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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2006年论文

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2006年论文

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name

Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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type

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study

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Alexander R Judkins

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Jaclyn A Biegel

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Marc K Rosenblum

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P2860

Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers

Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene.

INI1 expression is retained in composite rhabdoid tumors, including rhabdoid meningiomas

Central nervous system atypical teratoid/rhabdoid tumor: results of therapy in children enrolled in a registry

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.

Synchronous occurrence of malignant rhabdoid tumor two decades after Wilms' tumor irradiation.

Malignant rhabdoid meningioma arising in the setting of preexisting ganglioglioma: a diagnosis supported by fluorescence in situ hybridization. Case report.

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