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

Year Number of Results
1945 2
1946 2
1947 2
1948 1
1949 1
1950 3
1951 3
1952 6
1953 3
1954 6
1955 5
1956 8
1957 5
1958 15
1959 11
1960 10
1961 6
1962 12
1963 17
1964 71
1965 72
1966 65
1967 65
1968 84
1969 94
1970 141
1971 120
1972 104
1973 140
1974 138
1975 173
1976 181
1977 160
1978 185
1979 224
1980 218
1981 227
1982 195
1983 249
1984 239
1985 274
1986 254
1987 210
1988 219
1989 255
1990 313
1991 290
1992 306
1993 376
1994 368
1995 384
1996 416
1997 449
1998 483
1999 494
2000 519
2001 549
2002 559
2003 598
2004 582
2005 630
2006 706
2007 874
2008 879
2009 874
2010 947
2011 1036
2012 1193
2013 1212
2014 1227
2015 1283
2016 1254
2017 1331
2018 1363
2019 1468
2020 1577
2021 1641
2022 1589
2023 1464
2024 568

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30,864 results

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Quoted phrase not found in phrase index: "Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss"
Page 1
Sudden sensorineural hearing loss: a review of diagnosis, treatment, and prognosis.
Kuhn M, Heman-Ackah SE, Shaikh JA, Roehm PC. Kuhn M, et al. Trends Amplif. 2011 Sep;15(3):91-105. doi: 10.1177/1084713811408349. Epub 2011 May 22. Trends Amplif. 2011. PMID: 21606048 Free PMC article. Review.
Sudden sensorineural hearing loss (SSNHL) is commonly encountered in audiologic and otolaryngologic practice. SSNHL is most commonly defined as sensorineural hearing loss of 30 dB or greater over at least three contiguous audiometric freq …
Sudden sensorineural hearing loss (SSNHL) is commonly encountered in audiologic and otolaryngologic practice. SSNHL is …
Congenital Sensorineural Hearing Loss.
Shave S, Botti C, Kwong K. Shave S, et al. Pediatr Clin North Am. 2022 Apr;69(2):221-234. doi: 10.1016/j.pcl.2021.12.006. Pediatr Clin North Am. 2022. PMID: 35337535 Review.
Congenital sensorineural hearing loss is highly prevalent in our population, with a wide variety of causes. The key to clinical management is early detection and intervention, to promote language and cognitive development. With expanding genetic knowledge abo …
Congenital sensorineural hearing loss is highly prevalent in our population, with a wide variety of causes. The key to …
Sudden Sensorineural Hearing Loss: A Diagnostic and Therapeutic Emergency.
Prince ADP, Stucken EZ. Prince ADP, et al. J Am Board Fam Med. 2021 Jan-Feb;34(1):216-223. doi: 10.3122/jabfm.2021.01.200199. J Am Board Fam Med. 2021. PMID: 33452100 Free article. Review.
The family physician's role in recognizing and managing sudden sensorineural hearing loss (SSNHL) is crucial. A recently updated otolaryngologic clinical practice guideline has been released for this emergency syndrome, but dissemination is limited to a speci …
The family physician's role in recognizing and managing sudden sensorineural hearing loss (SSNHL) is crucial. A recentl …
Contemporary review of the causes and differential diagnosis of sudden sensorineural hearing loss.
Young YH. Young YH. Int J Audiol. 2020 Apr;59(4):243-253. doi: 10.1080/14992027.2019.1689432. Epub 2019 Nov 12. Int J Audiol. 2020. PMID: 31714154 Review.
Objectives: This article provides an overview of the causes and differential diagnosis of sudden deafness (SD) and sudden sensorineural hearing loss (SSHL).Design: Contemporary review.Study sample: This review is based on peer-reviewed articles published in t …
Objectives: This article provides an overview of the causes and differential diagnosis of sudden deafness (SD) and sudden sensorineural …
COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome.
Storey H, Savige J, Sivakumar V, Abbs S, Flinter FA. Storey H, et al. J Am Soc Nephrol. 2013 Dec;24(12):1945-54. doi: 10.1681/ASN.2012100985. Epub 2013 Sep 19. J Am Soc Nephrol. 2013. PMID: 24052634 Free PMC article.
Alport syndrome is an inherited disease characterized by hematuria, progressive renal failure, hearing loss, and ocular abnormalities. Autosomal recessive Alport syndrome is suspected in consanguineous families and when female patients develop renal failure. ...The …
Alport syndrome is an inherited disease characterized by hematuria, progressive renal failure, hearing loss, and ocular abnorm …
Harboyan Syndrome.
Javaid A, Orakzai AA. Javaid A, et al. J Ayub Med Coll Abbottabad. 2020 Oct-Dec;32(Suppl 1)(4):S701-S703. J Ayub Med Coll Abbottabad. 2020. PMID: 33754535 Free article.
Harboyan syndrome is a degenerative corneal disorder characterized by congenital hereditary endothelial dystrophy along with progressive, post lingual sensorineural hearing loss. We present the case of a 16-year-old female, who came to us for her follow up af …
Harboyan syndrome is a degenerative corneal disorder characterized by congenital hereditary endothelial dystrophy along with progressive, po …
The Dizzy Child.
Kelly EA, Janky KL, Patterson JN. Kelly EA, et al. Otolaryngol Clin North Am. 2021 Oct;54(5):973-987. doi: 10.1016/j.otc.2021.06.002. Epub 2021 Jul 23. Otolaryngol Clin North Am. 2021. PMID: 34304898 Review.
Vestibular dysfunction is commonly seen in patients with sensorineural hearing loss. Migraine disorders are the most common cause of dizziness in childhood. ...
Vestibular dysfunction is commonly seen in patients with sensorineural hearing loss. Migraine disorders are the most co …
Fluctuating Sensorineural Hearing Loss.
Liu H, Zhou K, Zhang X, Peng KA. Liu H, et al. Audiol Neurootol. 2019;24(3):109-116. doi: 10.1159/000500658. Epub 2019 Jul 17. Audiol Neurootol. 2019. PMID: 31315108 Free article. Review.
BACKGROUND: Several otologic conditions can present with fluctuating sensorineural hearing loss, including Meniere's disease, autoimmune inner ear disease, and enlarged vestibular aqueduct. ...SUMMARY: A literature search was performed regarding fluctuating …
BACKGROUND: Several otologic conditions can present with fluctuating sensorineural hearing loss, including Meniere's di …
Ototoxicity and Teprotumumab.
Highland J, Gordon S, Reddy D, Patel N. Highland J, et al. Ann Otol Rhinol Laryngol. 2022 Aug;131(8):910-913. doi: 10.1177/00034894211042740. Epub 2021 Aug 27. Ann Otol Rhinol Laryngol. 2022. PMID: 34448414
The aim of this report is to describe one of the first known cases of teprotumumab-induced irreversible sensorineural hearing loss. METHODS: Case report at a tertiary referral center. ...CONCLUSIONS: This is one of the first descriptive cases of ototoxicity r …
The aim of this report is to describe one of the first known cases of teprotumumab-induced irreversible sensorineural hearing …
Epstein Syndrome.
Barrah S, Kheder R, Jebali H, Krid M, Smaoui W, Beji S, Hmida FB, Fatma LB, Rais L, Zouaghi MK. Barrah S, et al. Saudi J Kidney Dis Transpl. 2020 Jul-Aug;31(4):865-867. doi: 10.4103/1319-2442.292323. Saudi J Kidney Dis Transpl. 2020. PMID: 32801250
Epstein syndrome is characterized by sensorineural hearing impairment, macro- thrombocytopenia without neutrophil inclusion bodies, and hereditary nephritis which can progress to end-stage renal disease (ESRD) in adolescence. ...
Epstein syndrome is characterized by sensorineural hearing impairment, macro- thrombocytopenia without neutrophil inclusion …
30,864 results
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