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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2004 1
2005 1
2006 1
2007 2
2009 2
2011 2
2012 2
2013 3
2014 2
2015 4
2016 4
2017 8
2018 7
2019 9
2020 13
2021 13
2022 20
2023 12
2024 7

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Similar articles for PMID: 38224868

101 results

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Page 1
Genetic diagnosis of childhood sensorineural hearing loss.
Reda Del Barrio S, García Fernández A, Quesada-Espinosa JF, Sánchez-Calvín MT, Gómez-Manjón I, Sierra-Tomillo O, Juárez-Rufián A, de Vergas Gutiérrez J. Reda Del Barrio S, et al. Acta Otorrinolaringol Esp (Engl Ed). 2024 Mar-Apr;75(2):83-93. doi: 10.1016/j.otoeng.2023.07.002. Epub 2024 Jan 13. Acta Otorrinolaringol Esp (Engl Ed). 2024. PMID: 38224868
Diagnostic yield of genetic testing in adults with sensorineural hearing loss.
Reda Del Barrio S, de Vergas Gutiérrez J, Quesada-Espinosa JF, Sánchez-Calvín MT, Gómez-Manjón I, Sierra-Tomillo O, Juárez-Rufián A, Fernández AG. Reda Del Barrio S, et al. Acta Otorrinolaringol Esp (Engl Ed). 2024 Feb 10:S2173-5735(24)00026-7. doi: 10.1016/j.otoeng.2023.10.007. Online ahead of print. Acta Otorrinolaringol Esp (Engl Ed). 2024. PMID: 38346493
Clinical utility of next-generation sequencing in the aetiological diagnosis of sensorineural hearing loss in a Childhood Hearing Loss Unit.
Costales M, Diñeiro M, Cifuentes GA, Capín R, Otero A, Viejo-Díaz M, Plasencia A, Núñez F, Gómez JR, Llorente JL, Cadiñanos J, Cabanillas R. Costales M, et al. Acta Otorrinolaringol Esp (Engl Ed). 2020 May-Jun;71(3):166-174. doi: 10.1016/j.otorri.2019.05.005. Epub 2019 Nov 6. Acta Otorrinolaringol Esp (Engl Ed). 2020. PMID: 31706454 English, Spanish.
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
Cabanillas R, Diñeiro M, Cifuentes GA, Castillo D, Pruneda PC, Álvarez R, Sánchez-Durán N, Capín R, Plasencia A, Viejo-Díaz M, García-González N, Hernando I, Llorente JL, Repáraz-Andrade A, Torreira-Banzas C, Rosell J, Govea N, Gómez-Martínez JR, Núñez-Batalla F, Garrote JA, Mazón-Gutiérrez Á, Costales M, Isidoro-García M, García-Berrocal B, Ordóñez GR, Cadiñanos J. Cabanillas R, et al. BMC Med Genomics. 2018 Jul 9;11(1):58. doi: 10.1186/s12920-018-0375-5. BMC Med Genomics. 2018. PMID: 29986705 Free PMC article.
Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults.
Corriols-Noval P, López Simón EC, Cadiñanos J, Diñeiro M, Capín R, González Aguado R, Costales Marcos M, Morales Angulo C, Cabanillas Farpón R. Corriols-Noval P, et al. Otol Neurotol. 2022 Dec 1;43(10):1125-1136. doi: 10.1097/MAO.0000000000003706. Epub 2022 Oct 3. Otol Neurotol. 2022. PMID: 36190904
Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.
Elander J, Ullmark T, Ehrencrona H, Jonson T, Piccinelli P, Samuelsson S, Löwgren K, Falkenius-Schmidt K, Ehinger J, Stenfeldt K, Värendh M. Elander J, et al. Int J Pediatr Otorhinolaryngol. 2022 Aug;159:111218. doi: 10.1016/j.ijporl.2022.111218. Epub 2022 Jun 24. Int J Pediatr Otorhinolaryngol. 2022. PMID: 35779349 Free article.
Early audiological phenotype in patients with mutations in the USH2A gene.
Markova TG, Lalayants MR, Alekseeva NN, Ryzhkova OP, Shatokhina OL, Galeeva NM, Bliznetz EA, Weener ME, Belov OA, Chibisova SS, Polyakov AV, Tavartkiladze GA. Markova TG, et al. Int J Pediatr Otorhinolaryngol. 2022 Jun;157:111140. doi: 10.1016/j.ijporl.2022.111140. Epub 2022 Apr 15. Int J Pediatr Otorhinolaryngol. 2022. PMID: 35452909
101 results