Glioma
What's New
Last Posted: Feb 13, 2024
- Evaluating the clinical utility of artificial intelligence assistance and its explanation on the glioma grading task.
Weina Jin et al. Artif Intell Med 2024 148102751 - Development and validation of a clinical prediction model for glioma grade using machine learning.
Mingzhen Wu et al. Technol Health Care 2024 - 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 - A comprehensive genomic study of 390 H3F3A-mutant pediatric and adult diffuse high-grade gliomas, CNS WHO grade 4.
Erik A Williams et al. Acta Neuropathol 2023 - A computer-aided diagnosis system for brain tumors based on artificial intelligence algorithms.
Tao Chen et al. Front Neurosci 2023 171120781 - A new era for glioma therapy - targeting mutant IDH.
David A Reardon et al. Nat Rev Clin Oncol 2023 7 - Significance of molecular diagnostics for therapeutic decision-making in recurrent glioma.
Jens Blobner et al. Neurooncol Adv 2023 5(1) vdad060 - Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With Glioma.
Patrick R Benusiglio et al. JCO Precis Oncol 2023 7e2200525 - Performance of deep learning algorithms to distinguish high-grade glioma from low-grade glioma: A systematic review and meta-analysis.
Wanyi Sun et al. iScience 2023 26(6) 106815 - Deep Learning Approaches for Glioblastoma Prognosis in Resource-Limited Settings: A Study using Basic Patient Demographic, Clinical, and Surgical Inputs.
Marc Ghanem et al. World Neurosurg
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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
- Page last updated:Mar 27, 2024
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