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

Year Number of Results
1971 3
1973 1
1975 13
1976 14
1977 13
1978 10
1979 6
1980 22
1981 21
1982 29
1983 29
1984 41
1985 29
1986 39
1987 32
1988 27
1989 50
1990 57
1991 57
1992 67
1993 87
1994 86
1995 73
1996 75
1997 88
1998 103
1999 134
2000 115
2001 111
2002 123
2003 141
2004 179
2005 207
2006 217
2007 255
2008 292
2009 292
2010 321
2011 420
2012 466
2013 475
2014 517
2015 538
2016 571
2017 558
2018 639
2019 718
2020 736
2021 823
2022 742
2023 743
2024 336

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10,050 results

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Quoted phrase not found in phrase index: "Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay"
Page 1
Classification and Current Management of Inner Ear Malformations.
Sennaroğlu L, Bajin MD. Sennaroğlu L, et al. Balkan Med J. 2017 Sep 29;34(5):397-411. doi: 10.4274/balkanmedj.2017.0367. Epub 2017 Aug 25. Balkan Med J. 2017. PMID: 28840850 Free PMC article.
Morphologically congenital sensorineural hearing loss can be investigated under two categories. The majority of congenital hearing loss causes (80%) are membranous malformations. Here, the pathology involves inner ear hair cells. . …
Morphologically congenital sensorineural hearing loss can be investigated under two categories. The majority of cong …
Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.
Mathur P, Yang J. Mathur P, et al. Biochim Biophys Acta. 2015 Mar;1852(3):406-20. doi: 10.1016/j.bbadis.2014.11.020. Epub 2014 Dec 4. Biochim Biophys Acta. 2015. PMID: 25481835 Free PMC article. Review.
Usher syndrome (USH), clinically and genetically heterogeneous, is the leading genetic cause of combined hearing and vision loss. USH is classified into three types, based on the hearing and vestibular symptoms observed in patients. Sixteen loci …
Usher syndrome (USH), clinically and genetically heterogeneous, is the leading genetic cause of combined hearing and vision …
Down Syndrome for the Otolaryngologist: A Review.
Zalzal HG, Lawlor CM. Zalzal HG, et al. JAMA Otolaryngol Head Neck Surg. 2023 Apr 1;149(4):360-367. doi: 10.1001/jamaoto.2023.0001. JAMA Otolaryngol Head Neck Surg. 2023. PMID: 36862403 Review.
OBSERVATIONS: A confluence of characteristics common to Down syndrome may be associated with issues in the head and neck, from infancy through adulthood. Hearing concerns range from narrow ear canals and cerumen impactions to eustachian tube dysfunctio …
OBSERVATIONS: A confluence of characteristics common to Down syndrome may be associated with issues in the head and neck, from …
Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?
Craeghs L, Goderis J, Acke F, Keymeulen A, Smets K, Van Hoecke H, De Leenheer E, Boudewyns A, Desloovere C, Kuhweide R, Muylle M, Royackers L, Schatteman I, Dhooge I. Craeghs L, et al. Ear Hear. 2021 Mar/Apr;42(2):373-380. doi: 10.1097/AUD.0000000000000927. Ear Hear. 2021. PMID: 32769435
Normal cUS and cMRI findings have a negative predictive value of 91% and 92%, respectively, for the development of delayed-onset hearing loss. CONCLUSIONS: Neuroimaging evidence of CNS involvement in the neonatal period is associated with the presence …
Normal cUS and cMRI findings have a negative predictive value of 91% and 92%, respectively, for the development of delayed-ons …
KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans.
Kalinousky AJ, Luperchio TR, Schrode KM, Harris JR, Zhang L, DeLeon VB, Fahrner JA, Lauer AM, Bjornsson HT. Kalinousky AJ, et al. Genes (Basel). 2023 Dec 28;15(1):48. doi: 10.3390/genes15010048. Genes (Basel). 2023. PMID: 38254937 Free PMC article.
Individuals with Kabuki syndrome type 1 (KS1) often have hearing loss recognized in middle childhood. ...Our data suggest that while ear infections and structural abnormalities contribute to the observed hearing loss, these …
Individuals with Kabuki syndrome type 1 (KS1) often have hearing loss recognized in middle childhood. ...Our data sugge …
Bilateral Congenital Ossicular Anomalies: Are the Anomalies Symmetric for Both Ears?
Yeon EK, Son HO, Sung HJ, Choi JW. Yeon EK, et al. Otolaryngol Head Neck Surg. 2023 Oct;169(4):1028-1034. doi: 10.1002/ohn.341. Epub 2023 Apr 1. Otolaryngol Head Neck Surg. 2023. PMID: 37003293
OBJECTIVE: To evaluate whether bilateral congenital ossicular anomalies (COAs) differ regarding ossicular anomalies and hearing loss severities between the ears of the individual. ...CONCLUSION: The severity of ossicular abnormalities and hea …
OBJECTIVE: To evaluate whether bilateral congenital ossicular anomalies (COAs) differ regarding ossicular anomalies and hearing …
Hearing Rehabilitation in Congenital Middle Ear Malformation.
Frenzel H. Frenzel H. Adv Otorhinolaryngol. 2018;81:32-42. doi: 10.1159/000485525. Epub 2018 Apr 6. Adv Otorhinolaryngol. 2018. PMID: 29794426 Review.
Microtia and atresia cause significant conductive hearing loss of up to 60 dB HL. The bilateral cases suffer from severely restricted communication abilities and require immediate acoustic stimulation. ...In conclusion, hearing rehabilitation of congenital …
Microtia and atresia cause significant conductive hearing loss of up to 60 dB HL. The bilateral cases suffer from severely res …
Otosclerosis under the magnifying glass.
Bălaşa Vîrzob CR, Cloşca RM, Poenaru M, Morar R, Balica NC, Sarău CA, Ioniţă I, Baderca F. Bălaşa Vîrzob CR, et al. Rom J Morphol Embryol. 2023 Apr-Jun;64(2):189-197. doi: 10.47162/RJME.64.2.09. Rom J Morphol Embryol. 2023. PMID: 37518876 Free PMC article.
In otosclerosis, the energy exerted by sound at the level of the tympanic membrane is reduced in the inner ear due to the fixation and rigidity of the ossicular chain, leading to hearing loss, especially for low frequencies. The primary clinical symptom of ot …
In otosclerosis, the energy exerted by sound at the level of the tympanic membrane is reduced in the inner ear due to the fixation an …
Thromboelastography predicting the prognosis of sudden sensorineural hearing loss.
Chen L, Wang Y, Gao X, Xiong W, Duan F, Zhang N, Wang H, Wang M. Chen L, et al. Clin Otolaryngol. 2022 Nov;47(6):724-731. doi: 10.1111/coa.13959. Epub 2022 Aug 1. Clin Otolaryngol. 2022. PMID: 35818895
The chi-squared test and binary logistic regression analysis were used to analyse the association between factors, such as vertigo, degree and type of hearing loss, vestibular function, inner ear MRI results, thromboelastography and efficacy of treatment. ... …
The chi-squared test and binary logistic regression analysis were used to analyse the association between factors, such as vertigo, degree a …
Audiologic and Otologic Clinical Manifestations of Loeys-Dietz Syndrome: A Heritable Connective Tissue Disorder.
Jeon JW, Christensen J, Chisholm J, Zalewski C, Rasooly M, Dempsey C, Magnani A, Frischmeyer-Guerrerio P, Brewer CC, Kim HJ. Jeon JW, et al. Otolaryngol Head Neck Surg. 2022 Feb;166(2):357-362. doi: 10.1177/01945998211008899. Epub 2021 May 11. Otolaryngol Head Neck Surg. 2022. PMID: 33971761 Free PMC article.
In LDS-1, 27% had bilateral conductive hearing loss; 9%, unilateral mixed; and 36%, subclinical. In LDS-2, 38% had conductive hearing loss and 38% subclinical. In LDS-3 and LDS-4, 40% and 43% had bilateral sensorineural hearing loss, resp …
In LDS-1, 27% had bilateral conductive hearing loss; 9%, unilateral mixed; and 36%, subclinical. In LDS-2, 38% had conductive …
10,050 results
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