Volumetric endpoints in diffuse intrinsic pontine glioma: comparison to cross-sectional measures and outcome correlations in the International DIPG/DMG Registry.
Lazow, MA; Nievelstein, MT; Lane, A; Bandopadhayhay, P; DeWire-Schottmiller, M; Fouladi, M; Glod, JW; Greiner, RJ; Hoffman, LM; Hummel, TR; et al.
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Phase I study of ribociclib and everolimus in children with newly diagnosed DIPG and high-grade glioma: A CONNECT pediatric neuro-oncology consortium report.
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Neuro-Oncology Advances.
2022;
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Overcoming barriers to establishing autopsy procurement programs in pediatric patients with central nervous system tumors: a call to develop regional centers.
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Journal of Neuro-Oncology.
2021;
152:107-114.
Characterizing temporal genomic heterogeneity in pediatric low-grade gliomas.
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Acta neuropathologica communications.
2020;
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Visual field outcomes in children treated for neurofibromatosis type 1-associated optic pathway gliomas: a multicenter retrospective study.
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A phase I/II study of ribociclib following radiation therapy in children with newly diagnosed diffuse intrinsic pontine glioma (DIPG).
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Journal of Neuro-Oncology.
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A Phase I and Pharmacokinetic Study of Oral Dabrafenib in Children and Adolescent Patients with Recurrent or Refractory BRAF V600 Mutation-Positive Solid Tumors.
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Clinical Cancer Research.
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Malignant peripheral nerve sheath tumor: Transformation in a patient with neurofibromatosis type 2.
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Pediatric Blood and Cancer.
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Pediatric intramedullary spinal cord tumor outcomes using the WeeFIM scale.
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Child's Nervous System.
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LGG-24. TEMPORAL GENOMIC HETEROGENEITY IN PEDIATRIC LOW-GRADE GLIOMAS.
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