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Results by year

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

Year Number of Results
1976 1
1978 1
1980 1
1981 1
1983 1
1987 1
1988 1
1989 1
1990 2
1991 1
1992 3
1993 3
1994 3
1995 4
1996 6
1997 7
1998 2
1999 4
2000 3
2001 3
2002 2
2003 3
2004 4
2005 2
2006 5
2007 5
2008 1
2009 3
2010 9
2011 2
2012 7
2013 2
2014 5
2015 11
2016 3
2017 5
2018 8
2019 7
2020 1
2021 5
2022 9
2024 3
2025 0

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PubMed for id: 335096

139 results

Results by year

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Page 1
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
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder.
Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, Qi Y, Lou X, Huang X, Shi Q, Chang S, Xiong W, Yin Z, Yu N, Zhao H, Wang J, Wang J, Salvi RJ, Petit C, Smith RJ, Wang Q. Zong L, et al. J Med Genet. 2015 Aug;52(8):523-31. doi: 10.1136/jmedgenet-2014-102961. Epub 2015 May 18. J Med Genet. 2015. PMID: 25986071 Free PMC article.
X-Linked Sensorineural Hearing Loss: A Literature Review.
Corvino V, Apisa P, Malesci R, Laria C, Auletta G, Franzé A. Corvino V, et al. Curr Genomics. 2018 Aug;19(5):327-338. doi: 10.2174/1389202919666171218163046. Curr Genomics. 2018. PMID: 30065609 Free PMC article. Review.
Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire.
Parekh B, Duncan JL, Samarakoon L, Melia M, Abalem MF, Andrews CA, Audo I, Ayala AR, Bradley C, Cheetham JK, Dagnelie G, Durham TA, Huckfeldt RM, Lacy GD, Malbin B, Michaelides M, Musch DC, Peck-Dimit N, Stingl K, Weng CY, Zmejkoski AZ, Jayasundera KT; Foundation Fighting Blindness Clinical Consortium Investigator Group. Parekh B, et al. Invest Ophthalmol Vis Sci. 2024 Jun 3;65(6):5. doi: 10.1167/iovs.65.6.5. Invest Ophthalmol Vis Sci. 2024. PMID: 38833260 Free PMC article.
Connexin Mutations and Hereditary Diseases.
Qiu Y, Zheng J, Chen S, Sun Y. Qiu Y, et al. Int J Mol Sci. 2022 Apr 12;23(8):4255. doi: 10.3390/ijms23084255. Int J Mol Sci. 2022. PMID: 35457072 Free PMC article. Review.
139 results