Esophageal Cancer
What's New
Last Posted: Feb 29, 2024
- Describing patterns of familial cancer risk in subfertile men using population pedigree data.
Joemy M Ramsay et al. Hum Reprod 2024 - Spatial Clusters of Cancer Mortality in Brazil: A Machine Learning Modeling Approach.
Bruno Casaes Teixeira et al. Int J Public Health 2023 681604789 - Machine learning applications for early detection of esophageal cancer: a systematic review.
Farhang Hosseini et al. BMC Med Inform Decis Mak 2023 23(1) 124 - The current state of artificial intelligence in endoscopic diagnosis of early esophageal squamous cell carcinoma.
Yuwei Pan et al. Front Oncol 2023 131198941 - Evaluation of Endoscopic Response Using Deep Neural Network in Esophageal Cancer Patients Who Received Neoadjuvant Chemotherapy.
Satoru Matsuda et al. Annals of surgical oncology 2023 - CAV1 Impacts the Tumor Immune Microenvironment and Has Potential Value of Predicting Response to Immunotherapy in Esophageal Cancer.
Zhang Runan et al. DNA and cell biology 2023 42(1) 27-42 - Deep Learning for the Diagnosis of Esophageal Cancer in Endoscopic Images: A Systematic Review and Meta-Analysis.
Islam Md Mohaimenul et al. Cancers 2022 14(23) - Landscape of RB1 alterations in 22,432 Chinese solid tumor patients.
Xu Guanghui et al. Annals of translational medicine 2022 10(16) 885 - Development and validation of a deep learning model to predict survival of patients with esophageal cancer.
Huang Chen et al. Frontiers in oncology 2022 12971190 - Clinical Utility of Circulating Tumor Cells for Predicting Major Histopathological Response after Neoadjuvant Chemoradiotherapy in Patients with Esophageal Cancer
X Gao et al, J Per Med, August 31, 2022
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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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