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Results by year

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

Year Number of Results
1995 2
1998 1
2000 1
2001 1
2002 1
2004 1
2008 1
2009 1
2012 1
2013 1
2014 1
2015 1
2016 2
2017 1
2018 1
2020 1
2021 2
2022 2
2024 0

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PubMed for id: 390743

19 results

Results by year

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Page 1
Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I-A Cross-sectional Study of Hearing Function in 111 Carriers.
JanssensdeVarebeke SPF, Moyaert J, Fransen E, Bulen B, Neesen C, Devroye K, van de Berg R, Pennings RJE, Topsakal V, Vanderveken O, Van Camp G, Van Rompaey V. JanssensdeVarebeke SPF, et al. Ear Hear. 2021 Nov-Dec 01;42(6):1508-1524. doi: 10.1097/AUD.0000000000001099. Ear Hear. 2021. PMID: 34369416 Free PMC article.
Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice.
García-García G, Berzal-Serrano A, García-Díaz P, Villanova-Aparisi R, Juárez-Rodríguez S, de Paula-Vernetta C, Cavallé-Garrido L, Jaijo T, Armengot-Carceller M, Millán JM, Aller E. García-García G, et al. Genes (Basel). 2020 Dec 7;11(12):1467. doi: 10.3390/genes11121467. Genes (Basel). 2020. PMID: 33297549 Free PMC article. Clinical Trial.
Molecular study of patients with auditory neuropathy.
Carvalho GM, Ramos PZ, Castilho AM, Guimarães AC, Sartorato EL. Carvalho GM, et al. Mol Med Rep. 2016 Jul;14(1):481-90. doi: 10.3892/mmr.2016.5226. Epub 2016 May 9. Mol Med Rep. 2016. PMID: 27177047
The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.
Zhao Y, Hosono K, Suto K, Ishigami C, Arai Y, Hikoya A, Hirami Y, Ohtsubo M, Ueno S, Terasaki H, Sato M, Nakanishi H, Endo S, Mizuta K, Mineta H, Kondo M, Takahashi M, Minoshima S, Hotta Y. Zhao Y, et al. J Hum Genet. 2014 Sep;59(9):521-8. doi: 10.1038/jhg.2014.65. Epub 2014 Jul 31. J Hum Genet. 2014. PMID: 25078356
19 results