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Support for "Disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia.
Khademi E, Alehabib E, Shandiz EE, Ahmadifard A, Andarva M, Jamshidi J, Rahimi-Aliabadi S, Pouriran R, Nejad FR, Mansoori N, Shahmohammadibeni N, Taghavi S, Shokraeian P, Akhavan-Niaki H, Paisán-Ruiz C, Darvish H, Ohadi M. Khademi E, et al. Among authors: pouriran r. Genet Test Mol Biomarkers. 2017 Aug;21(8):485-490. doi: 10.1089/gtmb.2016.0422. Epub 2017 Jul 19. Genet Test Mol Biomarkers. 2017. PMID: 28723299
A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.
Andarva M, Jamshidi J, Ghaedi H, Daftarian N, Emamalizadeh B, Alehabib E, Taghavi S, Pouriran R, Darvish H. Andarva M, et al. Among authors: pouriran r. Clin Exp Optom. 2018 Mar;101(2):255-259. doi: 10.1111/cxo.12599. Epub 2017 Sep 18. Clin Exp Optom. 2018. PMID: 28922694 Free article.
Acute bacterial meningitis in Iran: Systematic review and meta-analysis.
Houri H, Pormohammad A, Riahi SM, Nasiri MJ, Fallah F, Dabiri H, Pouriran R. Houri H, et al. Among authors: pouriran r. PLoS One. 2017 Feb 7;12(2):e0169617. doi: 10.1371/journal.pone.0169617. eCollection 2017. PLoS One. 2017. PMID: 28170400 Free PMC article. Review.
45 results