Patterns of neuronal Rhes as a novel hallmark of tauopathies. Read more about Patterns of neuronal Rhes as a novel hallmark of tauopathies.
Integrated molecular and clinical analysis of low-grade gliomas in children with neurofibromatosis type 1 (NF1). Read more about Integrated molecular and clinical analysis of low-grade gliomas in children with neurofibromatosis type 1 (NF1).
Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1. Read more about Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1.
The immunohistochemical, DNA methylation, and chromosomal copy number profile of cauda equina paraganglioma is distinct from extra-spinal paraganglioma. Read more about The immunohistochemical, DNA methylation, and chromosomal copy number profile of cauda equina paraganglioma is distinct from extra-spinal paraganglioma.
Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition. Read more about Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition.
Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic features. Read more about Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic features.
An update on the central nervous system manifestations of familial tumor predisposition syndromes. Read more about An update on the central nervous system manifestations of familial tumor predisposition syndromes.
cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas. Read more about cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas.
Loss of H3K27 trimethylation by immunohistochemistry is frequent in oligodendroglioma, IDH-mutant and 1p/19q-codeleted, but is neither a sensitive nor a specific marker. Read more about Loss of H3K27 trimethylation by immunohistochemistry is frequent in oligodendroglioma, IDH-mutant and 1p/19q-codeleted, but is neither a sensitive nor a specific marker.
Neuroglial stem cell-derived inflammatory pseudotumor (n-SCIPT): clinicopathologic characterization of a novel lesion of the lumbosacral spinal cord and nerve roots following intrathecal allogeneic stem cell intervention. Read more about Neuroglial stem cell-derived inflammatory pseudotumor (n-SCIPT): clinicopathologic characterization of a novel lesion of the lumbosacral spinal cord and nerve roots following intrathecal allogeneic stem cell intervention.
