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Journal of Neurosurgery. Pediatrics|June 5, 2012
Spinal cord ependymomas and myxopapillary ependymomas in the first 2 decades of life: a clinicopathological and immunohistochemical characterization of 19 casesJames H Stephen, Angela J Sievert, Peter J Madsen, et al.
Brain Pathology (Zurich, Switzerland)|February 19, 2013
Evaluation of histone 3 lysine 27 trimethylation (H3K27me3) and enhancer of Zest 2 (EZH2) in pediatric glial and glioneuronal tumors shows decreased H3K27me3 in H3F3A K27M mutant glioblastomasSriram Venneti, Mihir T Garimella, Lisa M Sullivan, et al.
Journal of Neuropathology and Experimental Neurology|June 14, 2011
p16INK4A and p14ARF tumor suppressor pathways are deregulated in malignant rhabdoid tumorsSriram Venneti, Paul Le, Daniel Martinez, et al.
The American Journal of Surgical Pathology|November 16, 2011
Epithelioid malignant peripheral nerve sheath tumor arising in a schwannoma, in a patient with "neuroblastoma-like" schwannomatosis and a novel germline SMARCB1 mutationJodi M Carter, Carolyn O'Hara, George Dundas, et al.
Frontiers in Pediatrics|June 28, 2024
A method for measuring mitochondrial DNA copy number in pediatric populationsSimran Maggo, Liam Y North, Aime Ozuna, et al.
Journal of Neurosurgery. Pediatrics|January 2, 2010
Surgical treatment of a clival-C2 atypical teratoid/rhabdoid tumorGregory G Heuer, Heather Kiefer, Alexander R Judkins, et al.
Pediatric Blood & Cancer|November 2, 2005
Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutationKristin Janson, Lucien A Nedzi, Odile David, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 12, 2009
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumorsEric M Jackson, Angela J Sievert, Xiaowu Gai, et al.
Cold Spring Harbor Molecular Case Studies|March 28, 2018
Transmission of a <i>TP53</i> germline mutation from unaffected male carrier associated with pediatric glioblastoma in his child and gestational choriocarcinoma in his female partnerJennifer A Cotter, Linda Szymanski, Catherine Karimov, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 13, 2005
Clinicopathologic and genetic profile of intracranial marginal zone lymphoma: a primary low-grade CNS lymphoma that mimics meningiomaPang-Hsien Tu, Caterina Giannini, Alexander R Judkins, et al.
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