The aim of this study was to improve the neuropathologic recognition and provide criteria for
the pathological diagnosis in the neurodegenerative diseases grouped as frontotemporal …

Thymic size and density were studied in 23 untreated patients with Graves' disease and 38
control subjects using computed tomography. Both thymic size and density were higher in …

EGFR amplification is a frequent genetic alteration in primary (de novo) glioblastomas, and
is often associated with structural alterations. Most common is variant III (EGFRvIII), which …

Olig2 is a recently identified transcription factor involved in the phenotype definition of cells
in the oligodendroglial lineage. The expression of Olig2 transcript has been demonstrated in …

Objective: To clarify the genetic, clinicopathologic, and neuroimaging characteristics of
patients with hereditary diffuse leukoencephalopathy with spheroids (HDLS) with the colony …

Primary CNS germ cell tumors (GCTs) are rare neoplasms predominantly observed in the
pediatric and young adult populations. In line with the hypothesis that the primordial germ cell …

Central nervous system high‐grade neuroepithelial tumors with BCOR alteration (CNS
HGNET‐BCOR) are a recently reported rare entity, identified as a small fraction of tumors …

This study was conducted to investigate the feasibility and survival benefits of combined
treatment with radiotherapy and temozolomide (TMZ), which has been covered by the national …

Background Chemokines are involved in multiple aspects of pathogenesis and cellular
trafficking in tumorigenesis. In this study, we report that the latest member of the CXC-type …

Epithelioid glioblastoma (E‐GBM) is a rare aggressive variant of IDH‐wildtype glioblastoma
newly recognized in the 2016 World Health Organization classification, composed …