Found: 15
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Relapse patterns and outcome after relapse in standard risk medulloblastoma: a report from the HIT-SIOP-PNET4 study.
- Published in:
- Journal of Neuro-Oncology, 2016, v. 129, n. 3, p. 515, doi. 10.1007/s11060-016-2202-1
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- Publication type:
- Article
A review of clinical and histological features of Spanish paediatric medulloblastomas during the last 21 years.
- Published in:
- Child's Nervous System, 2006, v. 22, n. 5, p. 466, doi. 10.1007/s00381-005-0004-4
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- Publication type:
- Article
Molecular characterisation defines clinically-actionable heterogeneity within Group 4 medulloblastoma and improves disease risk-stratification.
- Published in:
- Acta Neuropathologica, 2023, v. 145, n. 5, p. 651, doi. 10.1007/s00401-023-02566-0
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- Publication type:
- Article
Validation of the 'French Acute Lymphoblastic Leukaemia Study Group FRALLE prognostic index' for paediatric Philadelphia-chromosome acute lymphoblastic leukaemia.
- Published in:
- British Journal of Haematology, 2012, v. 156, n. 2, p. 284, doi. 10.1111/j.1365-2141.2011.08860.x
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- Publication type:
- Article
Pharmacogenetics of MicroRNAs and MicroRNAs Biogenesis Machinery in Pediatric Acute Lymphoblastic Leukemia.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091261
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- Publication type:
- Article
Intron 3 of the ARID5B gene: a hot spot for acute lymphoblastic leukemia susceptibility.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2013, v. 139, n. 11, p. 1879, doi. 10.1007/s00432-013-1512-3
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- Publication type:
- Article
Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0177421
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- Publication type:
- Article
Polymorphisms of the SLCO1B1 gene predict methotrexate-related toxicity in childhood acute lymphoblastic leukemia.
- Published in:
- Pediatric Blood & Cancer, 2011, v. 57, n. 4, p. 612, doi. 10.1002/pbc.23074
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- Publication type:
- Article
Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
- Published in:
- Human Mutation, 2005, v. 25, n. 1, p. 99, doi. 10.1002/humu.9299
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- Publication type:
- Article
Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patients.
- Published in:
- Human Mutation, 2001, v. 17, n. 5, p. 437, doi. 10.1002/humu.1129
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- Publication type:
- Article
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications.
- Published in:
- Human Mutation, 2001, v. 17, n. 5, p. 412, doi. 10.1002/humu.1117
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- Publication type:
- Article
A submicroscopic deletion of 11p13 associated with the WAGR syndrome.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 319, doi. 10.1034/j.1399-0004.2003.00051.x
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- Publication type:
- Article
A prospective biological study in relation to a family with Li-Fraumeni syndrome.
- Published in:
- Clinical & Translational Oncology, 2012, v. 14, n. 5, p. 396, doi. 10.1007/s12094-012-0815-1
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- Publication type:
- Article
Evidence in medulloblastomas.
- Published in:
- Clinical & Translational Oncology, 2010, v. 12, n. 4, p. 271, doi. 10.1007/s12094-010-0503-y
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- Publication type:
- Article
Reasons for the New Spanish Society of Paediatric Haematology and Oncology (SEHOP).
- Published in:
- 2008
- By:
- Publication type:
- Editorial