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Page 1
Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends.
Fattahi Z, Mohseni M, Beheshtian M, Jafarpour A, Jalalvand K, Keshavarzi F, Behravan H, Ghodratpour F, Zare Ashrafi F, Kalhor M, Azad M, Koshki M, Ghaziasadi A, Soveyzi M, Abdollahi A, Kiani SJ, Ataei-Pirkooh A, Rezaeiazhar I, Bokharaei-Salim F, Haghshenas MR, Babamahmoodi F, Mokhames Z, Soleimani A, Elahi Z, Ziaee M, Javanmard D, Ghafari S, Ezani A, Ansari Moghaddam A, Shahraki-Sanavi F, Hashemi Shahri SM, Azaran A, Yousefi F, Moattari A, Moghadami M, Fakhim H, Ataei B, Nasri E, Poortahmasebi V, Varshochi M, Mojtahedi A, Jalilian F, Khazeni M, Moradi A, Tabarraei A, Piroozmand A, Yahyapour Y, Bayani M, Tavangar F, Yaghoubi M, Keramat F, Tavakoli M, Jalali T, Pouriayevali MH, Salehi-Vaziri M, Khorram Khorshid HR, Najafipour R, Malekzadeh R, Kahrizi K, Jazayeri SM, Najmabadi H. Fattahi Z, et al. Among authors: beheshtian m. Arch Iran Med. 2022 Aug 1;25(8):508-522. doi: 10.34172/aim.2022.83. Arch Iran Med. 2022. PMID: 37543873 Free article.
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: beheshtian 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.
Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.
Mohseni M, Razzaghmanesh M, Parsi Mehr E, Zare H, Beheshtian M, Najmabadi H. Mohseni M, et al. Among authors: beheshtian m. Iran Biomed J. 2016 Sep;20(4):201-6. doi: 10.7508/ibj.2016.04.003. Epub 2016 Mar 27. Iran Biomed J. 2016. PMID: 27017198 Free PMC article.
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.
Fattahi Z, Kalhor Z, Fadaee M, Vazehan R, Parsimehr E, Abolhassani A, Beheshtian M, Zamani G, Nafissi S, Nilipour Y, Akbari MR, Kahrizi K, Kariminejad A, Najmabadi H. Fattahi Z, et al. Among authors: beheshtian m. Clin Genet. 2017 Mar;91(3):386-402. doi: 10.1111/cge.12810. Epub 2016 Jul 21. Clin Genet. 2017. PMID: 27234031
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. Arch Iran Med. 2016 Oct 1;19(10):720-728. Arch Iran Med. 2016. PMID: 27743438 Free PMC article. Review.
De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.
Edizadeh M, Vazehan R, Javadi F, Dehdahsi S, Fadaee M, Faraji Zonooz M, Parsimehr E, Ahangari F, Abolhassani A, Kalhor Z, Fattahi Z, Beheshtian M, Kariminejad A, Akbari MR, Najmabadi H, Nafissi S. Edizadeh M, et al. Among authors: beheshtian m. Arch Iran Med. 2017 Sep;20(9):617-620. Arch Iran Med. 2017. PMID: 29048924
SLC52A2 mutations cause SCABD2 phenotype: A second report.
Babanejad M, Adeli OA, Nikzat N, Beheshtian M, Azarafra H, Sadeghnia F, Mohseni M, Najmabadi H, Kahrizi K. Babanejad M, et al. Among authors: beheshtian m. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:195-199. doi: 10.1016/j.ijporl.2017.11.014. Epub 2017 Nov 20. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287867
40 results