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

Year Number of Results
1945 1
1946 2
1947 4
1948 3
1949 2
1950 4
1951 8
1952 5
1953 4
1954 3
1955 2
1956 3
1959 8
1960 3
1961 11
1962 3
1963 12
1964 33
1965 35
1966 30
1967 35
1968 57
1969 64
1970 76
1971 85
1972 57
1973 72
1974 101
1975 91
1976 93
1977 106
1978 80
1979 53
1980 47
1981 53
1982 41
1983 63
1984 70
1985 69
1986 64
1987 55
1988 64
1989 57
1990 72
1991 93
1992 73
1993 90
1994 87
1995 100
1996 90
1997 121
1998 123
1999 162
2000 194
2001 195
2002 196
2003 155
2004 172
2005 172
2006 175
2007 232
2008 235
2009 213
2010 301
2011 278
2012 306
2013 313
2014 341
2015 360
2016 372
2017 363
2018 360
2019 389
2020 438
2021 496
2022 545
2023 563
2024 158

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9,230 results

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Quoted phrase not found in phrase index: "Leukoencephalopathy, progressive, infantile-onset, with or without deafness"
Page 1
Molecular diagnosis of hereditary deafness and application of stepwise testing strategy.
Zeng BP, Xu HG, Mao L, Tang WX. Zeng BP, et al. Yi Chuan. 2023 Jan 20;45(1):29-41. doi: 10.16288/j.yczz.22-206. Yi Chuan. 2023. PMID: 36927636 Review.
Hereditary deafness is one of the most common sensory disorders in humans, and exhibits high genetic heterogeneity. ...In this review, we evaluate and discuss the utility of molecular diagnosis and the application of stepwise testing strategies in hereditary deafness
Hereditary deafness is one of the most common sensory disorders in humans, and exhibits high genetic heterogeneity. ...In this review …
Brain Plasticity and Rehabilitation with a Cochlear Implant.
McKay CM. McKay CM. Adv Otorhinolaryngol. 2018;81:57-65. doi: 10.1159/000485586. Epub 2018 Apr 6. Adv Otorhinolaryngol. 2018. PMID: 29794427 Review.
The functional changes that occur in the brain due to deafness may affect the way the auditory system processes sound after cochlear implantation. ...The functional plasticity that occurs in postlingually deaf adults during periods of deafness can both support and h …
The functional changes that occur in the brain due to deafness may affect the way the auditory system processes sound after cochlear …
The usher syndromes.
Keats BJ, Corey DP. Keats BJ, et al. Am J Med Genet. 1999 Sep 24;89(3):158-66. Am J Med Genet. 1999. PMID: 10704190 Review.
Patients with USH1 have severe to profound congenital hearing impairment, vestibular dysfunction, and retinal degeneration beginning in childhood, while those with USH2 have moderate to severe hearing impairment, normal vestibular function, and later onset of retinal degeneration …
Patients with USH1 have severe to profound congenital hearing impairment, vestibular dysfunction, and retinal degeneration beginning in chil …
Why American Sign Language Gloss Must Matter.
Supalla SJ, Cripps JH, Byrne AP. Supalla SJ, et al. Am Ann Deaf. 2017;161(5):540-551. doi: 10.1353/aad.2017.0004. Am Ann Deaf. 2017. PMID: 28238974 Review.
Deafness in the genomics era.
Shearer AE, Hildebrand MS, Sloan CM, Smith RJ. Shearer AE, et al. Hear Res. 2011 Dec;282(1-2):1-9. doi: 10.1016/j.heares.2011.10.001. Epub 2011 Oct 8. Hear Res. 2011. PMID: 22016077 Free PMC article. Review.
Our understanding of hereditary hearing loss has greatly improved since the discovery of the first human deafness gene. These discoveries have only accelerated due to the great strides in DNA sequencing technology since the completion of the human genome project. Here, we …
Our understanding of hereditary hearing loss has greatly improved since the discovery of the first human deafness gene. These discove …
Deafness: diagnosis and management.
Tonkin JP. Tonkin JP. Med J Aust. 1990 Jun 18;152(12):659-63. doi: 10.5694/j.1326-5377.1990.tb125426.x. Med J Aust. 1990. PMID: 2198446 Review. No abstract available.
Advances in hereditary deafness.
Tekin M, Arnos KS, Pandya A. Tekin M, et al. Lancet. 2001 Sep 29;358(9287):1082-90. doi: 10.1016/S0140-6736(01)06186-4. Lancet. 2001. PMID: 11589958 Review.
Progress in the Human Genome Project, availability of cochlea-specific cDNA libraries, and development of murine models of deafness have resulted in rapid discovery of many loci and corresponding genes for deafness. ...Mutations in one gene, connexin 26 (CX26
Progress in the Human Genome Project, availability of cochlea-specific cDNA libraries, and development of murine models of deafnes
Higher-order auditory areas in congenital deafness: Top-down interactions and corticocortical decoupling.
Kral A, Yusuf PA, Land R. Kral A, et al. Hear Res. 2017 Jan;343:50-63. doi: 10.1016/j.heares.2016.08.017. Epub 2016 Sep 13. Hear Res. 2017. PMID: 27637669 Free article. Review.
Since these layers play a central role for processing top-down influences, congenital deafness might interfere with the integration of top-down and bottom-up information flow. ...Current data indicate a reduced corticocortical functional coupling between cortical auditory …
Since these layers play a central role for processing top-down influences, congenital deafness might interfere with the integration o …
9,230 results