Last Posted: Mar 03, 2023
- Use of artificial intelligence for the diagnosis of cholesteatoma.
Christopher C Tseng et al. Laryngoscope investigative otolaryngology 2023 8(1) 201-211
- Application of high resolution computed tomography image assisted classification model of middle ear diseases based on 3D-convolutional neural network.
Su Ri et al. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2022 47(8) 1037-1048
- Artificial intelligence to classify ear disease from otoscopy: A systematic review and meta-analysis.
Habib Al-Rahim et al. Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery 2022
- Is it useful to use computerized tomography image-based artificial intelligence modelling in the differential diagnosis of chronic otitis media with and without cholesteatoma?
Eroglu Orkun et al. American journal of otolaryngology 2022 103395
- RhoA, ROCK-1, and ROCK-2 Gene Expression and Polymorphisms in Cholesteatoma Patients.
Görür Kemal, et al. The journal of international advanced otology 2021 11 (6) 530-535
- Association Between Earwax-Determinant Genotypes and Acquired Middle Ear Cholesteatoma in a Japanese Population.
Hara Satoshi, et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2021 3 1945998211000374
- Association of CARD8 Activating Polymorphism With Bone Erosion in Cholesteatoma Patients.
Sangal Neel, et al. The Laryngoscope 2020 5
- Deep Learning in Automated Region Proposal and Diagnosis of Chronic Otitis Media Based on Computed Tomography.
Wang Yan-Mei et al. Ear and hearing 2019 Sep
- Are human ATP-binding cassette transporter C11 and earwax associated with the incidence of cholesteatoma?
Nakagawa Hiroshi, et al. Medical hypotheses 2018 5 19-22
- The Allele 2 of the VNTR Polymorphism in the Gene That Encodes a Natural Inhibitor of IL-1?, IL-1RA Is Favorably Associated With Chronic Otitis Media.
Živkovi? Maja, et al. Clinical and experimental otorhinolaryngology 2018 2
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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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics 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.
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- Page last updated:Jun 07, 2023
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