about
Extracranial rhabdoid tumours: what we have learned so far and future directionsGenome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibitionMutations in LZTR1 add to the complex heterogeneity of schwannomatosisClinical, pathological, and molecular data on desmoplastic/nodular medulloblastoma: case studies and a review of the literature.Non-rhabdoid pediatric SMARCB1-deficient tumors: overlap between chordomas and malignant rhabdoid tumors?A Phase I Study of the CDK4/6 Inhibitor Ribociclib (LEE011) in Pediatric Patients with Malignant Rhabdoid Tumors, Neuroblastoma, and Other Solid Tumors.SegAnnDB: interactive Web-based genomic segmentation.Embryonic signature distinguishes pediatric and adult rhabdoid tumors from other SMARCB1-deficient cancers.Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastomaMolecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas.[Medulloblastoma in childhood: an heterogeneous disease requiring treatment adjustments to known risk factors].Prognostic classification of pediatric medulloblastoma based on chromosome 17p loss, expression of MYCC and MYCN, and Wnt pathway activation.ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome.Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation.Atypical teratoid/rhabdoid tumors-current concepts, advances in biology, and potential future therapies.Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.Extra-renal non-cerebral rhabdoid tumours.TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma.Cytogenetic prognostication within medulloblastoma subgroups.Medulloblastomas: update on a heterogeneous disease.Clinicopathologic prognostic factors in childhood atypical teratoid and rhabdoid tumor of the central nervous system: a multicenter study.Embryonal tumor with multilayered rosettes: diagnostic tools update and review of the literature.SWI/SNF chromatin remodeling and human malignancies.Retinoblastoma and Neuroblastoma Predisposition and Surveillance.Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.Embryonal tumors with multilayered rosettes in children: the SFCE experience.Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas.Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor.Cholinergic switch associated with morphological differentiation in neuroblastoma.MYC and MYCN amplification can be reliably assessed by aCGH in medulloblastoma.Efficacy of etanercept for the treatment of juvenile idiopathic arthritis according to the onset type.AT-06THE EXTRAORDINARY CHALLENGE OF TREATING PATIENTS WITH CONGENITAL RHABDOID TUMORS - DATA FROM FRANCE, RUSSIA AND THE EU-RHAB REGISTRY.VIP hypersecretion as primary or secondary syndrome in neuroblastoma: A retrospective study by the Société Française des Cancers de l'Enfant (SFCE).LG-33PEDIATRIC INFRATENTORIAL GANGLIOGLIOMA: RESULTS OF A SERIES OF 33 CHILDREN AND LITERATURE REVIEW.Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.High-Throughput Drug Screening Identifies Pazopanib and Clofilium Tosylate as Promising Treatments for Malignant Rhabdoid Tumors.Right to know and right to ignore in paediatric oncogenetics: Identifying biological causes, or seeking for meaning?Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations.
P50
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Franck Bourdeaut
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Franck Bourdeaut
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