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Risk factors for domain-specific neurocognitive outcome in pediatric survivors of a brain tumor in the posterior fossa—Results of the HIT 2000 trial.
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- Neuro-Oncology, 2024, v. 26, n. 11, p. 2113, doi. 10.1093/neuonc/noae092
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- Article
Quality of survival and cognitive performance in children treated for medulloblastoma in the PNET 4 randomized controlled trial.
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- Neuro-Oncology Practice, 2017, v. 4, n. 3, p. 161, doi. 10.1093/nop/npw028
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- Article
Improved risk-stratification for posterior fossa ependymoma of childhood considering clinical, histological and genetic features – a retrospective analysis of the HIT ependymoma trial cohort.
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- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0820-5
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- Article
Evidence of neural crest cell origin of a DICER1 mutant CNS sarcoma in a child with DICER1 syndrome and NRAS‐mutant neurocutaneous melanosis.
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- Neuropathology & Applied Neurobiology, 2022, v. 48, n. 6, p. 1, doi. 10.1111/nan.12830
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- Article
Molecular stratification of medulloblastoma: comparison of histological and genetic methods to detect Wnt activated tumours.
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- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 2, p. 135, doi. 10.1111/nan.12161
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- Article
Treatment of embryonal tumors with multilayered rosettes with carboplatin/etoposide induction and high-dose chemotherapy within the prospective P-HIT trial.
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- Neuro-Oncology, 2022, v. 24, n. 1, p. 127, doi. 10.1093/neuonc/noab100
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- Article
Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study.
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- Neuro-Oncology, 2021, v. 23, n. 9, p. 1597, doi. 10.1093/neuonc/noab136
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- Article
Local and systemic therapy of recurrent ependymoma in children and adolescents: short- and long-term results of the E-HIT-REZ 2005 study.
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- Neuro-Oncology, 2021, v. 23, n. 6, p. 1012, doi. 10.1093/neuonc/noaa276
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- Article
GENE-06. DISTINCT MOLECULAR SUBGROUPS OF TUMORS OF THE PINEAL REGION CORRELATE WITH CLINICAL PARAMETERS AND GENETIC ALTERATIONS.
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- Neuro-Oncology, 2019, v. 21, p. ii81, doi. 10.1093/neuonc/noz036.077
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- Article
Systematic comparison of MRI findings in pediatric ependymoblastoma with ependymoma and CNS primitive neuroectodermal tumor not otherwise specified.
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- Neuro-Oncology, 2015, v. 17, n. 8, p. 1157, doi. 10.1093/neuonc/nov063
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- Article
PROGNOSTIC SIGNIFICANCE OF CLINICAL, HISTOPATHOLOGICAL, AND MOLECULAR CHARACTERISTICS OF MEDULLOBLASTOMAS IN THE PROSPECTIVE HIT2000 MULTICENTER CLINICAL TRIAL COHORT.
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- Neuro-Oncology, 2014, v. 16, n. suppl_3, p. iii24, doi. 10.1093/neuonc/nou208.7
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- Article
Treatment of young children with CNS-primitive neuroectodermal tumors/pineoblastomas in the prospective multicenter trial HIT 2000 using different chemotherapy regimens and radiotherapy.
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- Neuro-Oncology, 2013, v. 15, n. 2, p. 224, doi. 10.1093/neuonc/nos292
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- Article
Treatment of young children with localized medulloblastoma by chemotherapy alone: Results of the prospective, multicenter trial HIT 2000 confirming the prognostic impact of histology.
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- Neuro-Oncology, 2011, v. 13, n. 6, p. 669, doi. 10.1093/neuonc/nor025
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- Article
Treatment of children under 4 years of age with medulloblastoma and ependymoma in the HIT2000/HIT-REZ 2005 trials: Neuropsychological outcome 5 years after treatment.
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0227693
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- Article
Pediatric pineoblastoma: A pooled outcome study of North American and Australian therapeutic data.
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- Neuro-Oncology Advances, 2022, v. 4, n. 1, p. 1, doi. 10.1093/noajnl/vdac056
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- Article
Focal versus craniospinal radiation for disseminated atypical teratoid/rhabdoid tumor following favorable response to systemic therapy.
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- Pediatric Blood & Cancer, 2023, v. 70, n. 7, p. 1, doi. 10.1002/pbc.30351
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- Article
A single supratentorial high-grade neuroepithelial tumor with two distinct BCOR mutations, exceptionally long complete remission and survival.
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- 2020
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- Publication type:
- journal article
Ependymoblastoma of the brainstem: MRI findings and differential diagnosis.
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- Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1132, doi. 10.1002/pbc.24915
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- Article
Supratentorial primitive neuroectodermal tumors of the central nervous system frequently harbor deletions of the CDKN2A locus and other genomic aberrations distinct from medulloblastomas.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 9, p. 839, doi. 10.1002/gcc.20471
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- Article
Clinically relevant molecular hallmarks of PFA ependymomas display intratumoral heterogeneity and correlate with tumor morphology.
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- Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-023-02682-x
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- Article
Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohorts.
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- Acta Neuropathologica, 2023, v. 145, n. 1, p. 97, doi. 10.1007/s00401-022-02522-4
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- Article
Clinical and molecular heterogeneity of pineal parenchymal tumors: a consensus study.
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- Acta Neuropathologica, 2021, v. 141, n. 5, p. 771, doi. 10.1007/s00401-021-02284-5
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- Article
ETMR: a tumor entity in its infancy.
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- Acta Neuropathologica, 2020, v. 140, n. 3, p. 249, doi. 10.1007/s00401-020-02182-2
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- Article
CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort.
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- Acta Neuropathologica, 2020, v. 140, n. 3, p. 405, doi. 10.1007/s00401-020-02169-z
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- Article
Molecular subgrouping of primary pineal parenchymal tumors reveals distinct subtypes correlated with clinical parameters and genetic alterations.
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- Acta Neuropathologica, 2020, v. 139, n. 2, p. 243, doi. 10.1007/s00401-019-02101-0
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- Article
Frequency, Risk-Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Database.
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- Pediatric Blood & Cancer, 2011, v. 57, n. 6, p. 978, doi. 10.1002/pbc.23236
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- Article
Large cell/anaplastic medulloblastoma: Outcome according to myc status, histopathological, and clinical risk factors.
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- Pediatric Blood & Cancer, 2010, v. 54, n. 3, p. 369, doi. 10.1002/pbc.22339
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- Article
Rapid DNA methylation-based classification of pediatric brain tumors from ultrasonic aspirate specimens.
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- Journal of Neuro-Oncology, 2024, v. 169, n. 1, p. 73, doi. 10.1007/s11060-024-04702-6
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- Article
Clinical and molecular characterization of isolated M1 disease in pediatric medulloblastoma: experience from the German HIT-MED studies.
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- Journal of Neuro-Oncology, 2022, v. 157, n. 1, p. 37, doi. 10.1007/s11060-021-03913-5
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- Article
Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91.
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- Journal of Neuro-Oncology, 2007, v. 81, n. 2, p. 217, doi. 10.1007/s11060-006-9221-2
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- Article
Risk prediction in early childhood sonic hedgehog medulloblastoma treated with radiation-avoiding chemotherapy: Evidence for more than 2 subgroups.
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- Neuro-Oncology, 2023, v. 25, n. 8, p. 1518, doi. 10.1093/neuonc/noad027
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- Article
c-MYC expression sensitizes medulloblastoma cells to radio- and chemotherapy and has no impact on response in medulloblastoma patients.
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- BMC Cancer, 2011, v. 11, n. 1, p. 74, doi. 10.1186/1471-2407-11-74
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- Article
Impairment of intellectual functions after surgery and posterior fossa irradiation in children with ependymoma is related to age and neurologic complications.
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- 2008
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- Publication type:
- journal article
Impairment of intellectual functions after surgery and posterior fossa irradiation in children with ependymoma is related to age and neurologic complications.
- Published in:
- BMC Cancer, 2008, v. 8, p. 1, doi. 10.1186/1471-2407-8-15
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- Article