Found: 14
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Comprehensive analysis of diverse low-grade neuroepithelial tumors with FGFR1 alterations reveals a distinct molecular signature of rosette-forming glioneuronal tumor.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01027-z
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- Publication type:
- Article
An unusual recurrent high-grade glioneuronal tumor with MAP2K1 mutation and CDKN2A/B homozygous deletion.
- Published in:
- 2019
- By:
- Publication type:
- Letter
HGG-14. PEDIATRIC BITHALAMIC DIFFUSE GLIOMAS ARE DISTINGUISHED FROM THEIR UNILATERAL COUNTERPARTS BY FREQUENT EGFR EXON 20 INSERTIONS AND RARE HISTONE H3 MUTATIONS.
- Published in:
- Neuro-Oncology, 2019, v. 21, p. ii89, doi. 10.1093/neuonc/noz036.108
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- Publication type:
- Article
Meteorologist's profile: Hayman Rooke (1723-1806).
- Published in:
- Weather (00431656), 2011, v. 66, n. 12, p. 335, doi. 10.1002/wea.747
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- Publication type:
- Article
Intracranial mesenchymal tumors with FET‐CREB fusion are composed of at least two epigenetic subgroups distinct from meningioma and extracranial sarcomas.
- Published in:
- Brain Pathology, 2022, v. 32, n. 4, p. 1, doi. 10.1111/bpa.13037
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- Publication type:
- Article
Intracranial mesenchymal tumor with FET‐CREB fusion—A unifying diagnosis for the spectrum of intracranial myxoid mesenchymal tumors and angiomatoid fibrous histiocytoma‐like neoplasms.
- Published in:
- Brain Pathology, 2021, v. 31, n. 4, p. 1, doi. 10.1111/bpa.12918
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- Publication type:
- Article
Detection of glioma infiltration at the tumor margin using quantitative stimulated Raman scattering histology.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91648-8
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- Publication type:
- Article
Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 4, p. 747, doi. 10.1007/s00401-022-02478-5
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- Publication type:
- Article
Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic features.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 5, p. 953, doi. 10.1007/s00401-020-02144-8
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- Publication type:
- Article
Neuroglial stem cell-derived inflammatory pseudotumor (n-SCIPT): clinicopathologic characterization of a novel lesion of the lumbosacral spinal cord and nerve roots following intrathecal allogeneic stem cell intervention.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Recurrent non-canonical histone H3 mutations in spinal cord diffuse gliomas.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Primary intracranial sarcomas with DICER1 mutation often contain prominent eosinophilic cytoplasmic globules and can occur in the setting of neurofibromatosis type 1.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 3, p. 521, doi. 10.1007/s00401-019-01960-x
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- Publication type:
- Article
Schimke immunoosseous dysplasia: suggestions of genetic diversity.
- Published in:
- Human Mutation, 2007, v. 28, n. 3, p. 273, doi. 10.1002/humu.20432
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- Publication type:
- Article
Systemic and Craniospinal Rosai Dorfman Disease with Intraparenchymal, Intramedullary and Leptomeningeal Disease .
- Published in:
- 2021
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- Publication type:
- Case Study