Found: 18
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Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patterns.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51529-w
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- Publication type:
- Article
Synchronous T-lymphoblastic lymphoma and neuroblastoma in a 3-yr-old with novel germline SMARCA4 and EZH2 variants.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2023, v. 9, n. 4, p. 1, doi. 10.1101/mcs.a006286
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- Publication type:
- Article
Precision oncology for children: A primer for paediatricians.
- Published in:
- Paediatrics & Child Health (1205-7088), 2023, v. 28, n. 5, p. 278, doi. 10.1093/pch/pxac123
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- Publication type:
- Article
Syndromes Predisposing to Pediatric Central Nervous System Tumors: Lessons Learned and New Promises.
- Published in:
- Current Neurology & Neuroscience Reports, 2012, v. 12, n. 2, p. 153, doi. 10.1007/s11910-011-0244-5
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- Publication type:
- Article
Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt Leukemia.
- Published in:
- Current Oncology, 2023, v. 30, n. 7, p. 5946, doi. 10.3390/curroncol30070444
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- Publication type:
- Article
Non‐rhabdomyosarcoma soft tissue sarcomas diagnosed in patients at a young age. An overview of clinical, pathological, and molecular findings.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 8, p. 1, doi. 10.1002/pbc.29022
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- Publication type:
- Article
Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 8, p. 1, doi. 10.1002/pbc.29021
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- Publication type:
- Article
TERT promotor variant associated with poor clinical outcome in a patient with novel RBM15‐MKL1 fusion‐positive pediatric acute megakaryoblastic leukemia.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 1, p. 1, doi. 10.1002/pbc.28542
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- Publication type:
- Article
Considerations for the use of circulating tumor DNA sequencing as a screening tool in cancer predisposition syndromes.
- Published in:
- Pediatric Blood & Cancer, 2020, v. 67, n. 12, p. 1, doi. 10.1002/pbc.28758
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- Publication type:
- Article
Cost-effectiveness of early cancer surveillance for patients with Li-Fraumeni syndrome.
- Published in:
- 2019
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- Publication type:
- journal article
Retrospective evaluation of a decision-support algorithm (MIPOGG) for genetic referrals for children with neuroblastic tumors.
- Published in:
- 2018
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- Publication type:
- journal article
DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center.
- Published in:
- 2018
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- Publication type:
- journal article
Pediatric imaging in DICER1 syndrome.
- Published in:
- 2017
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- Publication type:
- journal article
Two congenital cases of pigmented epithelioid melanocytoma with unique clinical and genetic features.
- Published in:
- Dermatology Online Journal, 2023, v. 29, n. 5, p. 1, doi. 10.5070/D329562403
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- Publication type:
- Article
Diagnostic accuracy of imaging approaches for early tumor detection in children with Li-Fraumeni syndrome.
- Published in:
- Pediatric Radiology, 2022, v. 52, n. 7, p. 1283, doi. 10.1007/s00247-022-05296-9
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- Publication type:
- Article
Congenital midline spinal hamartoma in an infant with DICER1 syndrome: A case report.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.963768
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- Publication type:
- Article
Inherent diagnostic and treatment challenges in germinoma of the basal ganglia: a case report and review of the literature.
- Published in:
- Journal of Neuro-Oncology, 2008, v. 88, n. 3, p. 309, doi. 10.1007/s11060-008-9568-7
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- Publication type:
- Article
An eHealth decision‐support tool to prioritize referral practices for genetic evaluation of patients with Wilms tumor.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 4, p. 1010, doi. 10.1002/ijc.32561
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- Publication type:
- Article