about
Rapidly progressive dementia due to Mycobacterium neoaurum meningoencephalitisK27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomasPathology, Molecular Genetics, and Epigenetics of Diffuse Intrinsic Pontine GliomaIdentification of human brain tumour initiating cellsIdentification of a cancer stem cell in human brain tumorsAngiography-negative primary central nervous system vasculitis in children: a newly recognized inflammatory central nervous system diseaseGenomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutationsCombined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersFunctionally defined therapeutic targets in diffuse intrinsic pontine gliomaTelomerase inhibition abolishes the tumorigenicity of pediatric ependymoma tumor-initiating cells.Histopathological spectrum of paediatric diffuse intrinsic pontine glioma: diagnostic and therapeutic implications.Basal ganglia germinoma in children with associated ipsilateral cerebral and brain stem hemiatrophy.Temporal lobe surgery for intractable epilepsy in children: an analysis of outcomes in 126 children.Inherent diagnostic and treatment challenges in germinoma of the basal ganglia: a case report and review of the literature.Management and outcome of chordomas in the pediatric population: The Hospital for Sick Children experience and review of the literature.Pediatric high-grade glioma: biologically and clinically in need of new thinkingGenome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomasGenome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.ATM regulates 3-methylpurine-DNA glycosylase and promotes therapeutic resistance to alkylating agents.Genomic analysis of diffuse pediatric low-grade gliomas identifies recurrent oncogenic truncating rearrangements in the transcription factor MYBL1A microRNA-1280/JAG2 network comprises a novel biological target in high-risk medulloblastoma.Human telomere reverse transcriptase expression predicts progression and survival in pediatric intracranial ependymoma.MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism.Substrate reduction therapy in juvenile GM2 gangliosidosis.Personalizing the treatment of pediatric medulloblastoma: Polo-like kinase 1 as a molecular target in high-risk children.Medulloblastoma subgroups remain stable across primary and metastatic compartments.A GATA4-regulated tumor suppressor network represses formation of malignant human astrocytomas.Viruses and human brain tumors: cytomegalovirus enters the fray.Primary central nervous system sarcomas in children: clinical, radiological, and pathological features.Study of the biodistribution of fluorescein in glioma-infiltrated mouse brain and histopathological correlation of intraoperative findings in high-grade gliomas resected under fluorescein fluorescence guidance.Alkylpurine-DNA-N-glycosylase confers resistance to temozolomide in xenograft models of glioblastoma multiforme and is associated with poor survival in patientsPatients with primary brain tumors as organ donors: case report and review of the literature.GATA6 is an astrocytoma tumor suppressor gene identified by gene trapping of mouse glioma model.Rapid, reliable, and reproducible molecular sub-grouping of clinical medulloblastoma samplesEmbryonal tumors with abundant neuropil and true rosettes: a distinctive CNS primitive neuroectodermal tumor.Pilomyxoid astrocytoma in a patient with neurofibromatosis.B7-H3, a potential therapeutic target, is expressed in diffuse intrinsic pontine glioma.Medulloblastoma subgroup-specific outcomes in irradiated children: who are the true high-risk patients?Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma.Differential transformation capacity of neuro-glial progenitors during development
P50
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P50
name
Cynthia Hawkins
@ast
Cynthia Hawkins
@en
Cynthia Hawkins
@nl
type
label
Cynthia Hawkins
@ast
Cynthia Hawkins
@en
Cynthia Hawkins
@nl
prefLabel
Cynthia Hawkins
@ast
Cynthia Hawkins
@en
Cynthia Hawkins
@nl