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The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.
PLoS One. 2015 Aug 26;10(8):e0129631. doi: 10.1371/journal.pone.0129631. eCollection 2015.
PLoS One. 2015.
PMID: 26308914
Free PMC article.
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
Davarnia B, Babanejad M, Fattahi Z, Nikzat N, Bazazzadegan N, Pirzade A, Farajollahi R, Nishimura C, Jalalvand K, Arzhangi S, Kahrizi K, Smith RJ, Najmabadi H.
Davarnia B, et al. Among authors: farajollahi r.
Int J Pediatr Otorhinolaryngol. 2012 Feb;76(2):268-71. doi: 10.1016/j.ijporl.2011.11.019. Epub 2011 Dec 14.
Int J Pediatr Otorhinolaryngol. 2012.
PMID: 22172221
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GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.
Abbaspour Rodbaneh E, Panahi M, Rahimi B, Mokabber H, Farajollahi R, Davarnia B.
Abbaspour Rodbaneh E, et al. Among authors: farajollahi r.
J Clin Lab Anal. 2021 Nov;35(11):e24024. doi: 10.1002/jcla.24024. Epub 2021 Sep 28.
J Clin Lab Anal. 2021.
PMID: 34581455
Free PMC article.
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De novo KAT6B mutation causes Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome in an Iranian boy: a case report.
Davarnia B, Panahi M, Rahimi B, Anari H, Farajollahi R, Rodbaneh EA, Jeddi F.
Davarnia B, et al. Among authors: farajollahi r.
J Med Case Rep. 2024 Jan 5;18(1):4. doi: 10.1186/s13256-023-04237-w.
J Med Case Rep. 2024.
PMID: 38178270
Free PMC article.
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Discriminatory Precision of Renal Angina Index in Predicting Acute Kidney Injury in Children; a Systematic Review and Meta-Analysis.
Abbasi A, Mehdipour Rabori P, Farajollahi R, Mohammed Ali K, Ataei N, Yousefifard M, Hosseini M.
Abbasi A, et al. Among authors: farajollahi r.
Arch Acad Emerg Med. 2020 Mar 26;8(1):e39. eCollection 2020.
Arch Acad Emerg Med. 2020.
PMID: 32259128
Free PMC article.
Review.
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