Ewing Sarcoma
What's New
Last Posted: Aug 18, 2022
- Prospective Clinical Genomic Profiling of Ewing Sarcoma: ERF and FGFR1 Mutations as Recurrent Secondary Alterations of Potential Biologic and Therapeutic Relevance.
Ogura Koichi et al. JCO precision oncology 2022 6e2200048 - Development of a Machine Learning-Based Predictive Model for Lung Metastasis in Patients With Ewing Sarcoma.
Li Wenle et al. Frontiers in medicine 2022 9807382 - Construction and validation of nomograms for non-metastatic Ewing sarcoma: A prognostic factor analysis based on the SEER database.
Huang Runzhi et al. Oncology letters 2021 22(5) 777 - Germline Variation and Somatic Alterations in Ewing Sarcoma.
Machiela Mitchell J et al. Methods in molecular biology (Clifton, N.J.) 2021 22263-14 - Gene expression and immunohistochemical analyses identify SOX2 as major risk factor for overall survival and relapse in Ewing sarcoma patients.
Sannino Giuseppina et al. EBioMedicine 2019 Sep 47156-162 - Precision medicine in Ewing sarcoma: a translational point of view.
Gargallo P et al. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2020 Feb - Omic approaches to pediatric bone sarcomas.
Tirtei Elisa et al. Pediatric blood & cancer 2019 Nov e28072 - Machine learning-based prediction of response to PARP inhibition across cancer types.
KE Hill et al, MedRXIV, September 27, 2019 - Precision medicine approaches for the management of Ewing sarcoma: current perspectives.
Rizk Victoria T et al. Pharmacogenomics and personalized medicine 2019 129-14 - Clinical Utility of In Situ Hybridization Assays in Head and Neck Neoplasms.
Luk Peter P et al. Head and neck pathology 2018 Nov
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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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