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

Year Number of Results
1964 1
1968 2
1970 2
1971 2
1972 1
1973 1
1974 4
1976 1
1977 1
1978 2
1979 2
1980 2
1982 2
1983 4
1984 1
1985 4
1986 1
1987 1
1988 6
1989 5
1990 6
1991 4
1992 5
1993 3
1994 8
1995 9
1996 12
1997 14
1998 15
1999 8
2000 11
2001 15
2002 7
2003 9
2004 9
2005 6
2006 16
2007 9
2008 13
2009 18
2010 18
2011 25
2012 20
2013 10
2014 17
2015 29
2016 14
2017 26
2018 13
2019 15
2020 18
2021 24
2022 32
2023 15
2024 3

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466 results

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Page 1
Congenital hearing loss.
Korver AM, Smith RJ, Van Camp G, Schleiss MR, Bitner-Glindzicz MA, Lustig LR, Usami SI, Boudewyns AN. Korver AM, et al. Nat Rev Dis Primers. 2017 Jan 12;3:16094. doi: 10.1038/nrdp.2016.94. Nat Rev Dis Primers. 2017. PMID: 28079113 Free PMC article. Review.
Congenital hearing loss (hearing loss that is present at birth) is one of the most prevalent chronic conditions in children. ...Genetic causes probably account for the majority of cases in developed countries; mutations can affect any component of the hearing pathway, in p …
Congenital hearing loss (hearing loss that is present at birth) is one of the most prevalent chronic conditions in children. ...Genet …
Usher Syndrome: Genetics of a Human Ciliopathy.
Fuster-García C, García-Bohórquez B, Rodríguez-Muñoz A, Aller E, Jaijo T, Millán JM, García-García G. Fuster-García C, et al. Int J Mol Sci. 2021 Jun 23;22(13):6723. doi: 10.3390/ijms22136723. Int J Mol Sci. 2021. PMID: 34201633 Free PMC article. Review.
In the retina, the USH protein network is principally located in the periciliary region of the photoreceptors, and plays an important role in the maintenance of the periciliary structure and the trafficking of molecules between the inner and the outer segments of photorece …
In the retina, the USH protein network is principally located in the periciliary region of the photoreceptors, and plays an important role i …
The Facial Nerve: Anatomy and Pathology.
Ottaiano AC, Gomez GD, Freddi TAL. Ottaiano AC, et al. Semin Ultrasound CT MR. 2023 Apr;44(2):71-80. doi: 10.1053/j.sult.2022.11.005. Epub 2022 Nov 28. Semin Ultrasound CT MR. 2023. PMID: 37055142 Review.
After leaving the brainstem, the facial nerve divides into 5 intracranial segments (cisternal, canalicular, labyrinthine, tympanic, and mastoid) and continues as the intraparotid extracranial segment (2). A wide variety of pathologies, including congenital abnormalities …
After leaving the brainstem, the facial nerve divides into 5 intracranial segments (cisternal, canalicular, labyrinthine, tympanic, and mast …
Cochlear synaptopathy in acquired sensorineural hearing loss: Manifestations and mechanisms.
Liberman MC, Kujawa SG. Liberman MC, et al. Hear Res. 2017 Jun;349:138-147. doi: 10.1016/j.heares.2017.01.003. Epub 2017 Jan 10. Hear Res. 2017. PMID: 28087419 Free PMC article. Review.
Recent studies in animal models suggest, however, that well before this overt hearing loss can be seen, a more insidious, but likely more common, process is taking place that permanently interrupts synaptic communication between sensory inner hair cells and subsets of coch …
Recent studies in animal models suggest, however, that well before this overt hearing loss can be seen, a more insidious, but likely more co …
SOX10: 20 years of phenotypic plurality and current understanding of its developmental function.
Pingault V, Zerad L, Bertani-Torres W, Bondurand N. Pingault V, et al. J Med Genet. 2022 Feb;59(2):105-114. doi: 10.1136/jmedgenet-2021-108105. Epub 2021 Oct 19. J Med Genet. 2022. PMID: 34667088 Free PMC article. Review.
All of these diseases are consistent with the regulatory role of SOX10 in various neural crest derivatives (melanocytes, the enteric nervous system, Schwann cells and olfactory ensheathing cells) and extraneural crest tissues (inner ear, oligodendrocytes). The recen …
All of these diseases are consistent with the regulatory role of SOX10 in various neural crest derivatives (melanocytes, the enteric nervous …
The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.
Delmaghani S, El-Amraoui A. Delmaghani S, et al. Hum Genet. 2022 Apr;141(3-4):709-735. doi: 10.1007/s00439-022-02448-7. Epub 2022 Mar 30. Hum Genet. 2022. PMID: 35353227 Free PMC article. Review.
Cochlear implants are currently used to reduce the burden of hearing loss in severe-to-profoundly deaf patients, but many promising treatments including gene, cell, and drug therapies to restore the native function of the inner ear and retinal sensory cells are unde …
Cochlear implants are currently used to reduce the burden of hearing loss in severe-to-profoundly deaf patients, but many promising treatmen …
Analysis between phenotypes and genotypes of inner ear malformation.
Wang S, Ding W, Chen C, Xu B, Liu X, Bian P, Guo Y. Wang S, et al. Acta Otolaryngol. 2019 Mar;139(3):223-232. doi: 10.1080/00016489.2018.1554262. Epub 2019 Feb 14. Acta Otolaryngol. 2019. PMID: 30762457 Review.
METHODS: Sixty EVA patients were tested by audiometry, temporal bone high-resolution CT and inner ear MRI. SNPscan technology were carried out after the patients signed informed consent. SPSS19.0 software was used. RESULT: 1. Three types malformations include …
METHODS: Sixty EVA patients were tested by audiometry, temporal bone high-resolution CT and inner ear MRI. SNPscan technology …
Third Window Lesions.
Ho ML. Ho ML. Neuroimaging Clin N Am. 2019 Feb;29(1):57-92. doi: 10.1016/j.nic.2018.09.005. Neuroimaging Clin N Am. 2019. PMID: 30466645 Review.
Third window abnormalities are bony defects of the inner ear that enable abnormal communication with the middle ear and/or cranial cavity. ...
Third window abnormalities are bony defects of the inner ear that enable abnormal communication with the middle ear …
Pendred syndrome.
Wémeau JL, Kopp P. Wémeau JL, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):213-224. doi: 10.1016/j.beem.2017.04.011. Epub 2017 May 10. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648509 Review.
The hallmark of the syndrome is the impaired hearing, which is associated with inner ear malformations such as an enlarged vestibular aqueduct (EVA). ...Pendrin has affinity for chloride, iodide, and bicarbonate, among other anions. In the inner ear …
The hallmark of the syndrome is the impaired hearing, which is associated with inner ear malformations such as an enlar …
Meniere's disease.
Nakashima T, Pyykkö I, Arroll MA, Casselbrant ML, Foster CA, Manzoor NF, Megerian CA, Naganawa S, Young YH. Nakashima T, et al. Nat Rev Dis Primers. 2016 May 12;2:16028. doi: 10.1038/nrdp.2016.28. Nat Rev Dis Primers. 2016. PMID: 27170253 Review.
Meniere's disease (MD) is a disorder of the inner ear that causes vertigo attacks, fluctuating hearing loss, tinnitus and aural fullness. ...The diagnosis of MD is based on clinical symptoms but can be complemented with functional inner ear tests, incl …
Meniere's disease (MD) is a disorder of the inner ear that causes vertigo attacks, fluctuating hearing loss, tinnitus and aura …
466 results