Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup

(2018) Pascal D. Johann et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Molecular and Clinicopathologic Heterogeneity of Intracranial Tumors Mimicking Extraskeletal Myxoid Chondrosarcoma

(2018) Julia Velz et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

DNA methylation-based classification of central nervous system tumours

(2018) David Capper et al.   NATURE

Magnetic resonance imaging surrogates of molecular subgroups in atypical teratoid / rhabdoid tumor (ATRT)

(2018) Johannes Nowak et al.   NEURO-ONCOLOGY

A Systematic Review of Atypical Teratoid Rhabdoid Tumor in Adults

(2018) Vivien Chan et al.   Frontiers in Oncology

Announcing cIMPACT-NOW: the Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy

(2016) David N. Louis et al.   ACTA NEUROPATHOLOGICA

Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis

(2016) Martin Hasselblatt et al.   ACTA NEUROPATHOLOGICA

Atypical teratoid/rhabdoid tumors with multilayered rosettes in the pineal region

(2016) Junmei Wang et al.   Brain Tumor Pathology

Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors

(2016) Jonathon Torchia et al.   CANCER CELL

Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes

(2016) Pascal D. Johann et al.   CANCER CELL

Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies

(2016) Michael C. Frühwald et al.   NEURO-ONCOLOGY

Meningeal SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily B member 1 (SMARCB1)-deficient tumours: an emerging group of meningeal tumours

(2016) B. Dadone et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Atypical Teratoid/Rhabdoid Tumor of the Pineal Region in a Young Adult Male Patient: Case Report and Review of the Literature

(2016) Axel Florschütz et al.   Journal of Neurological Surgery Part A-Central European Neurosurgery

SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis

(2014) Martin Hasselblatt et al.   ACTA NEUROPATHOLOGICA

Pilomyxoid astrocytoma of the pineal region: Cytopathological features and differential diagnostic considerations by intraoperative smear preparation

(2014) Toshitetsu Hayashi et al.   DIAGNOSTIC CYTOPATHOLOGY

Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing

(2014) Volker Hovestadt et al.   NATURE

Atypical teratoid rhabdoid tumor located in the pineal region following prophylactic irradiation for acute lymphoblastic leukemia

(2012) Atsushi Kuge et al.   Brain Tumor Pathology

High-resolution genomic analysis suggests the absence of recurrent genomic alterations other thanSMARCB1aberrations in atypical teratoid/rhabdoid tumors

(2012) Martin Hasselblatt et al.   GENES CHROMOSOMES & CANCER

Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions

(2012) Lisa M Sullivan et al.   MODERN PATHOLOGY

Pineal chordoid meningioma complicated by repetitive hemorrhage during pregnancy: Case report and literature review

(2012) Kyung-Hwa Lee et al.   NEUROPATHOLOGY

Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome

(2010) Reinhard Schneppenheim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor

(2009) Uwe Kordes et al.   GENES CHROMOSOMES & CANCER

Chordoid meningioma arising in the pineal region: a case report

(2008) Shintaro Fukushima et al.   Brain Tumor Pathology

Myxoid chondrosarcoma in the pineal region

(2008) Takatoshi Sorimachi et al.   JOURNAL OF NEUROSURGERY