Lack of classical astroblastoma features in pediatric <scp>MN1</scp>::<scp>BEND2</scp>‐fused brain tumors-Reference-Cited by-同舟云学术

Lack of classical astroblastoma features in pediatric MN1::BEND2‐fused brain tumors

Published:2024-09-05 Issue: Volume: Page:
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Chapman Nicholas¹^ORCID,Iqbal Mohammed²,Walker Adam D.³,Hawes Debra³⁴,Davidson Tom Belle⁴⁵,Robison Nathan⁴⁵,Tamrazi Benita⁴⁶,Ji Jianling³⁴,Krieger Mark D.¹⁴,Cotter Jennifer A.³⁴

Affiliation:

1. Department of Surgery and Division of Neurosurgery Children's Hospital Los Angeles Los Angeles California USA

2. Department of Neurosurgery University of Texas, Dell Medical School Austin Texas USA

3. Department of Pathology & Laboratory Medicine Children's Hospital Los Angeles Los Angeles California USA

4. Keck School of Medicine University of Southern California Los Angeles California United States

5. Cancer and Blood Disease Institute, Children's Hospital Los Angeles Los Angeles California USA

6. Department of Radiology Children's Hospital Los Angeles Los Angeles California USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.13297

Reference9 articles.

1. Molecular Profiling Reclassifies Adult Astroblastoma into Known and Clinically Distinct Tumor Entities with Frequent Mitogen-Activated Protein Kinase Pathway Alterations

2. Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review

3. Multimodal molecular analysis of astroblastoma enables reclassification of most cases into more specific molecular entities

4. The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion

5. Targeted fusion analysis can aid in the classification and treatment of pediatric glioma, ependymoma, and glioneuronal tumors