Found: 17
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Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome.
- Published in:
- Genes, Chromosomes & Cancer, 2024, v. 63, n. 1, p. 1, doi. 10.1002/gcc.23195
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- Publication type:
- Article
Non-Malignant Cerebrospinal Fluid Ascites in a Patient with Atypical Teratoid Rhabdoid Tumor.
- Published in:
- Oncology Research & Treatment, 2017, v. 40, n. 4, p. 216, doi. 10.1159/000458441
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- Publication type:
- Article
DNA-methylation subgroups carry no prognostic significance in ATRT-SHH patients in clinical trial cohorts.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 3, p. 543, doi. 10.1007/s00401-023-02614-9
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- Publication type:
- Article
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases.
- Published in:
- Acta Neuropathologica, 2021, v. 141, n. 2, p. 291, doi. 10.1007/s00401-020-02250-7
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- Publication type:
- Article
Infratentorial C11orf95-fused gliomas share histologic, immunophenotypic, and molecular characteristics of supratentorial RELA-fused ependymoma.
- Published in:
- Acta Neuropathologica, 2020, v. 140, n. 6, p. 963, doi. 10.1007/s00401-020-02238-3
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- Publication type:
- Article
Chromosome arm 1q gain is an adverse prognostic factor in localized and diffuse leptomeningeal glioneuronal tumors with BRAF gene fusion and 1p deletion.
- Published in:
- 2019
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- Publication type:
- Case Study
Outcomes for children with recurrent/refractory atypical teratoid rhabdoid tumor: A single‐institution study with molecular correlation.
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 10, p. 1, doi. 10.1002/pbc.31208
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- Publication type:
- Article
A rare manifestation of choriocarcinoma syndrome in a child with primary intracranial germ cell tumor and extracranial metastases: A case report and review of the literature.
- Published in:
- 2021
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- Publication type:
- journal article
Comment on: Response to the BRAF/MEK inhibitors dabrafenib/trametinib in an adolescent with a BRAF V600E mutated anaplastic ganglioglioma intolerant to vemurafenib.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 4, p. 1, doi. 10.1002/pbc.28814
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- Publication type:
- Article
Treatment-related calvarial lesions in pediatric brain tumor survivors.
- Published in:
- 2020
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- Publication type:
- journal article
Malignant progression of a peripheral nerve sheath tumor in the setting of rhabdoid tumor predisposition syndrome.
- Published in:
- 2018
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- Publication type:
- journal article
Mortality in children with low-grade glioma or glioneuronal tumors: A single-institution study.
- Published in:
- 2018
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- Publication type:
- journal article
Atypical teratoid/rhabdoid tumour‐TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition.
- Published in:
- Neuropathology & Applied Neurobiology, 2024, v. 50, n. 2, p. 1, doi. 10.1111/nan.12971
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- Publication type:
- Article
High-grade glioma in infants and young children is histologically, molecularly, and clinically diverse: Results from the SJYC07 trial and institutional experience.
- Published in:
- Neuro-Oncology, 2024, v. 26, n. 1, p. 178, doi. 10.1093/neuonc/noad130
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- Publication type:
- Article
Phase II study of alisertib as a single agent for treating recurrent or progressive atypical teratoid/rhabdoid tumor.
- Published in:
- Neuro-Oncology, 2023, v. 25, n. 2, p. 386, doi. 10.1093/neuonc/noac151
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- Publication type:
- Article
Molecular grouping and outcomes of young children with newly diagnosed ependymoma treated on the multi-institutional SJYC07 trial.
- Published in:
- Neuro-Oncology, 2019, v. 21, n. 10, p. 1319, doi. 10.1093/neuonc/noz069
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- Publication type:
- Article
Brainstem Low-Grade Gliomas in Children—Excellent Outcomes With Multimodality Therapy.
- Published in:
- Journal of Child Neurology, 2017, v. 32, n. 2, p. 194, doi. 10.1177/0883073816675547
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- Publication type:
- Article