The link between inner ear malformations and the rest of the body: what we know so far about genetic, imaging and histology
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Clinical Neurology,Radiology Nuclear Medicine and imaging
Link
http://link.springer.com/content/pdf/10.1007/s00234-020-02382-3.pdf
Reference22 articles.
1. Sennaroglu L (2016) Histopathology of inner ear malformations: do we have enough evidence to explain pathophysiology? Cochlear Implants Int 17:3–20. https://doi.org/10.1179/1754762815Y.0000000016
2. D’Arco F, Youssef A, Ioannidou E, et al. (2019) Temporal bone and intracranial abnormalities in syndromic causes of hearing loss: an updated guide, Eur J Radiol. 26;123:108803. doi: https://doi.org/10.1016/j.ejrad.2019.108803
3. Koffler T, Ushakov K, Avraham KB (2015) Genetics of hearing loss: syndromic. Otolaryngol Clin N Am 48:1041–1061. https://doi.org/10.1016/j.otc.2015.07.007
4. P.M. Som, H.D. Curtin, K. Liu et al. (2016) Current embryology of the temporal bone, part I: the inner ear. Neurographics 6(4):250 –265; doi:https://doi.org/10.3174/ng.4160166
5. Parsa CF, Robert MP (2013) Thromboembolism and congenital malformations: from Duane syndrome to thalidomide embryopathy. JAMA Ophthalmol 131(4):439–447
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