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

Year Number of Results
1991 1
2000 2
2002 2
2003 2
2004 1
2005 5
2006 2
2007 5
2008 3
2009 5
2010 3
2011 6
2012 5
2013 3
2014 4
2015 6
2016 4
2017 5
2018 8
2019 7
2020 10
2021 3
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81 results
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Page 1
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H. Sloan-Heggen CM, et al. Among authors: daneshi a. J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7. J Med Genet. 2015. PMID: 26445815 Free PMC article.
Impact of Acamprosate on Chronic Tinnitus: A Randomized-Controlled Trial.
Farhadi M, Salem MM, Asghari A, Daneshi A, Mirsalehi M, Mahmoudian S. Farhadi M, et al. Among authors: daneshi a. Ann Otol Rhinol Laryngol. 2020 Nov;129(11):1110-1119. doi: 10.1177/0003489420930773. Epub 2020 Jun 5. Ann Otol Rhinol Laryngol. 2020. PMID: 32500717 Clinical Trial.
Titanium Snoreplasty- A New Surgical Technique.
Daneshi A, Jahandideh H, Hosseinzadeh F. Daneshi A, et al. Iran J Otorhinolaryngol. 2020 Jan;32(108):29-34. doi: 10.22038/ijorl.2019.31930.2051. Iran J Otorhinolaryngol. 2020. PMID: 32083028 Free PMC article.
New marsupialization technique in endolymphatic sac surgery.
Daneshi A, Hosseinzadeh F, Mohebbi S, Mohseni M, Mohammadi SS, Asghari A. Daneshi A, et al. Laryngoscope Investig Otolaryngol. 2020 May 26;5(3):546-551. doi: 10.1002/lio2.403. eCollection 2020 Jun. Laryngoscope Investig Otolaryngol. 2020. PMID: 32596499 Free PMC article.
Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
Beheshtian M, Babanejad M, Azaiez H, Bazazzadegan N, Kolbe D, Sloan-Heggen C, Arzhangi S, Booth K, Mohseni M, Frees K, Azizi MH, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Najmabadi H. Beheshtian M, et al. Among authors: daneshi a. Arch Iran Med. 2016 Oct 1;19(10):720-728. Arch Iran Med. 2016. PMID: 27743438 Free PMC article. Review.
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
Bazazzadegan N, Sheffield AM, Sobhani M, Kahrizi K, Meyer NC, Van Camp G, Hilgert N, Abedini SS, Habibi F, Daneshi A, Nishimura C, Avenarius MR, Farhadi M, Smith RJ, Najmabadi H. Bazazzadegan N, et al. Among authors: daneshi a. Am J Med Genet A. 2011 May;155A(5):1202-11. doi: 10.1002/ajmg.a.33209. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484990 Free PMC article. Review.
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