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

Year Number of Results
1999 1
2000 2
2001 1
2002 5
2003 4
2004 1
2005 7
2006 1
2007 4
2008 7
2009 3
2010 6
2011 11
2012 15
2013 25
2014 14
2015 16
2016 16
2017 15
2018 16
2019 17
2020 19
2021 34
2022 23
2023 36
2024 18

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282 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: farhadi m. 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.
Photobiomodulation therapy in mood disorders: a systematic review.
Montazeri K, Farhadi M, Fekrazad R, Chaibakhsh S, Mahmoudian S. Montazeri K, et al. Among authors: farhadi m. Lasers Med Sci. 2022 Dec;37(9):3343-3351. doi: 10.1007/s10103-022-03641-w. Epub 2022 Nov 21. Lasers Med Sci. 2022. PMID: 36404359 Review.
The Danish Head and Neck Cancer Group (DAHANCA) 2020 radiotherapy guidelines.
Jensen K, Friborg J, Hansen CR, Samsøe E, Johansen J, Andersen M, Smulders B, Andersen E, Nielsen MS, Eriksen JG, Petersen JBB, Elstrøm UV, Holm AI, Farhadi M, Morthorst MH, Skyt PS, Overgaard J, Grau C. Jensen K, et al. Among authors: farhadi m. Radiother Oncol. 2020 Oct;151:149-151. doi: 10.1016/j.radonc.2020.07.037. Epub 2020 Aug 8. Radiother Oncol. 2020. PMID: 32781011 No abstract available.
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: farhadi m. Arch Iran Med. 2016 Oct 1;19(10):720-728. Arch Iran Med. 2016. PMID: 27743438 Free PMC article. Review.
Rehabilitation of children with cochlear implant in Iran: A scoping review.
Moradi M, Fallahi-Khoshknab M, Dalvandi A, Farhadi M, Maddah SSB, Mohammadi E. Moradi M, et al. Among authors: farhadi m. Med J Islam Repub Iran. 2021 Jun 7;35:73. doi: 10.47176/mjiri.35.73. eCollection 2021. Med J Islam Repub Iran. 2021. PMID: 34290997 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: farhadi m. 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.
282 results