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Year Number of Results
2002 4
2004 1
2016 1
2019 1
2020 1
2021 2
2022 1
2023 1
2024 1

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Page 1
Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection.
De Cuyper E, Acke F, Keymeulen A, De Leenheer EMR, Van Hoecke H, Padalko E, Boudewyns A, Gilles A, Muylle M, Kuhweide R, Royackers L, Desloovere C, Verstreken M, Schatteman I, Dhooge I. De Cuyper E, et al. Among authors: schatteman i. JAMA Otolaryngol Head Neck Surg. 2023 Feb 1;149(2):122-130. doi: 10.1001/jamaoto.2022.4109. JAMA Otolaryngol Head Neck Surg. 2023. PMID: 36580312 Free PMC article.
Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection.
De Cuyper E, Acke F, Keymeulen A, De Leenheer E, Van Hoecke H, Padalko E, Boudewyns A, Gilles A, Muylle M, Kuhweide R, Royackers L, Desloovere C, Verstreken M, Schatteman I, Dhooge I. De Cuyper E, et al. Among authors: schatteman i. JAMA Otolaryngol Head Neck Surg. 2024 Jan 1;150(1):30-38. doi: 10.1001/jamaoto.2023.3507. JAMA Otolaryngol Head Neck Surg. 2024. PMID: 37917050
Insufficient evidence for a role of SERPINF1 in otosclerosis.
Valgaeren H, Sommen M, Beyens M, Vandeweyer G, Schrauwen I, Schepers A, Schatteman I, Topsakal V, Dhooge I, Kunst H, Zanetti D, Huber AM, Hoischen A, Fransen E, Van Camp G. Valgaeren H, et al. Among authors: schatteman i. Mol Genet Genomics. 2019 Aug;294(4):1001-1006. doi: 10.1007/s00438-019-01558-8. Epub 2019 Apr 9. Mol Genet Genomics. 2019. PMID: 30968248
Clinical presentation of DFNA8-DFNA12.
Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE. Govaerts PJ, et al. Among authors: schatteman i. Adv Otorhinolaryngol. 2002;61:60-5. doi: 10.1159/000066805. Adv Otorhinolaryngol. 2002. PMID: 12408064 No abstract available.
Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?
Craeghs L, Goderis J, Acke F, Keymeulen A, Smets K, Van Hoecke H, De Leenheer E, Boudewyns A, Desloovere C, Kuhweide R, Muylle M, Royackers L, Schatteman I, Dhooge I. Craeghs L, et al. Among authors: schatteman i. Ear Hear. 2021 Mar/Apr;42(2):373-380. doi: 10.1097/AUD.0000000000000927. Ear Hear. 2021. PMID: 32769435
The use of malleus allografts in ossiculoplasty.
Vercruysse JP, Offeciers FE, Somers T, Schatteman I, Govaerts PJ. Vercruysse JP, et al. Among authors: schatteman i. Laryngoscope. 2002 Oct;112(10):1782-4. doi: 10.1097/00005537-200210000-00014. Laryngoscope. 2002. PMID: 12368615
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, Reardon W, Stephens D, Cremers CW, Smith RJ, Van Camp G. Cryns K, et al. Among authors: schatteman i. Hum Genet. 2002 May;110(5):389-94. doi: 10.1007/s00439-002-0719-1. Epub 2002 Apr 9. Hum Genet. 2002. PMID: 12073007
12 results