Ependymoma
What's New
Last Posted: Sep 19, 2023
- Deep learning based clinico-radiological model for paediatric brain tumor detection and subtype prediction.
Abhishek Mahajan et al. Explor Target Antitumor Ther 2023 4(4) 669-684 - MYB/MYBL1::QKI fusion-positive diffuse glioma.
Suh Ye Yoon et al. Journal of neuropathology and experimental neurology 2023 - Next-generation Sequencing of Cerebrospinal Fluid for Clinical Molecular Diagnostics in Pediatric, Adolescent and Young Adult (AYA) Brain Tumor Patients.
Miller Alexandra M et al. Neuro-oncology 2022 - Artificial Intelligence Applications in Pediatric Brain Tumor Imaging: A Systematic Review.
Huang Jonathan et al. World neurosurgery 2021 - Automatic Machine Learning to Differentiate Pediatric Posterior Fossa Tumors on Routine MR Imaging.
Zhou H et al. AJNR. American journal of neuroradiology 2020 Jul 41(7) 1279-1285 - Targeted next-generation sequencing of pediatric neuro-oncology patients improves diagnosis, identifies pathogenic germline mutations, and directs targeted therapy.
Kline Cassie N et al. Neuro-oncology 2017 19(5) 699-709 - Effect of a detailed family history of melanoma on risk for other tumors: a cohort study based on the nationwide Swedish Family-Cancer Database.
- Anaplastic ependymoma
From NCATS Genetic and Rare Diseases Information Center - Ependymoma
From NCATS Genetic and Rare Diseases Information Center - Myxopapillary ependymoma
From NCATS Genetic and Rare Diseases Information Center
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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