Sudden Sensorineural Hearing Loss
What's New
Last Posted: Feb 01, 2024
- A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss.
Mª Á Yélamos Lorente, et al. The Laryngoscope 2024 0 - Causal associations of thyroid function and sudden sensorineural hearing loss: a bidirectional and multivariable Mendelian randomization study.
Jialei Chen, et al. Frontiers in neurology 2023 0 1269545 - Machine Learning Models for Predicting Sudden Sensorineural Hearing Loss Outcome: A Systematic Review.
Amirhossein Aghakhani et al. Ann Otol Rhinol Laryngol 2023 34894231206902 - Clinical role of vitamin D, vitamin B12, folate levels and hematological parameters in patients with sudden sensorineural hearing loss.
Nurdan Kose Celebi, et al. Acta oto-laryngologica 2023 0 1-6 - The association of genetic polymorphisms in protocadherin 15 with sudden sensorineural hearing loss in a Chinese population.
Ying Lan, et al. Journal of clinical laboratory analysis 2023 0 e24896 - Glucocorticoid receptor (NR3C1) genetic polymorphisms and the outcomes of sudden sensorineural hearing loss.
Chien Chen-Yu, et al. Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale 2023 0 (1) 13 - Inflammatory markers and the risk of idiopathic sudden sensorineural hearing loss: A Mendelian randomization study.
Zhou Tingfeng, et al. Frontiers in neurology 2023 0 1111255 - Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review.
Cao Zaizai, et al. Audiology & neuro-otology 2019 0 (1) 8-19 - Deafness gene screening based on a multilevel cascaded BPNN model.
Xiao Liu et al. BMC bioinformatics 2023 24(1) 56 - Association between the 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene and sudden sensorineural hearing loss in Caucasian population: a meta-analysis.
Wei Zhenxing, et al. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2020 0 (7) 2203-2208
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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
- Page last updated:May 03, 2024
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