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Page 1
Incidence of infectious diseases after earthquakes: a systematic review and meta-analysis.
Najafi S, Akahavan Rezayat A, Beyzaei SF, Shahriari Z, Taheri Tabar M, Ghasemi Nour M, Mosaed R, Khadem-Rezaiyan M, Hamidi Farahani R. Najafi S, et al. Public Health. 2022 Jan;202:131-138. doi: 10.1016/j.puhe.2021.11.005. Epub 2021 Dec 23. Public Health. 2022. PMID: 34953295 Review.
The association between the incidences of infectious diseases before and after earthquakes was significant, namely, 1.561 (95% CI: 1.244-1.957) with a P-value <0.001. CONCLUSIONS: The results show an increase in the prevalence of infectious diseases after earthquakes. . …
The association between the incidences of infectious diseases before and after earthquakes was significant, namely, 1.561 (95% CI: 1.244-1.9 …
The mutation spectrum and ethnic distribution of non-hepatorenal tyrosinemia (types II, III).
Beyzaei Z, Nabavizadeh S, Karimzadeh S, Geramizadeh B. Beyzaei Z, et al. Orphanet J Rare Dis. 2022 Dec 5;17(1):424. doi: 10.1186/s13023-022-02579-0. Orphanet J Rare Dis. 2022. PMID: 36471409 Free PMC article. Review.
Thirty-three TAT variants have been reported in 42 families, consisting of 21 missense variants, 5 frameshift variants, 4 nonsense variants, 2 variants that primarily cause splicing site, and 1 skipping complete exon (large deletion). The most common variant is p.Arg57Ter, …
Thirty-three TAT variants have been reported in 42 families, consisting of 21 missense variants, 5 frameshift variants, 4 nonsense variants, …
Identification of a novel mutation in the ALDOB gene in hereditary fructose intolerance.
Beyzaei Z, Ezgu F, Imanieh MH, Haghighat M, Dehghani SM, Honar N, Geramizadeh B. Beyzaei Z, et al. J Pediatr Endocrinol Metab. 2023 Jan 23;36(3):331-334. doi: 10.1515/jpem-2022-0566. Print 2023 Mar 28. J Pediatr Endocrinol Metab. 2023. PMID: 36659819
The results of TGS showed a rare novel homozygous pathogenic variant c.944del (p.Gly315ValfsTer15) in the ALDOB gene. CONCLUSIONS: This report introduces a novel variant that expands the mutational spectrum of the ALDOB gene in patients with HFI....
The results of TGS showed a rare novel homozygous pathogenic variant c.944del (p.Gly315ValfsTer15) in the ALDOB gene. CONCLUSIONS: Th …
Novel PRKAG2 variant presenting as liver cirrhosis: report of a family with 2 cases and review of literature.
Beyzaei Z, Ezgu F, Geramizadeh B, Alborzi A, Shojazadeh A. Beyzaei Z, et al. BMC Med Genomics. 2021 Jan 28;14(1):33. doi: 10.1186/s12920-021-00879-1. BMC Med Genomics. 2021. PMID: 33509202 Free PMC article.
The echocardiography was a normal. CONCLUSION: A novel heterozygous variant c.592A > T (p.Met198Leu) expands the mutational spectrum of the PRKAG2 gene in this family. ...
The echocardiography was a normal. CONCLUSION: A novel heterozygous variant c.592A > T (p.Met198Leu) expands the mutational spectr …
Quercetin-loaded F127 nanomicelles: Antioxidant activity and protection against renal injury induced by gentamicin in rats.
Rahdar A, Hasanein P, Bilal M, Beyzaei H, Kyzas GZ. Rahdar A, et al. Life Sci. 2021 Jul 1;276:119420. doi: 10.1016/j.lfs.2021.119420. Epub 2021 Mar 27. Life Sci. 2021. PMID: 33785340
Remaining two groups received Q and NEQ (50 mg/kg, i.g.) plus GM (100 mg/kg, i.p.) simultaneously for 10 days. After the experiments, serum and kidneys were used for biochemical, molecular and histological examinations. ...
Remaining two groups received Q and NEQ (50 mg/kg, i.g.) plus GM (100 mg/kg, i.p.) simultaneously for 10 days. After the experiments, …
De Novo Donor Specific Antibody and Long-Term Outcome After Liver Transplantation: A Systematic Review and Meta-Analysis.
Beyzaei Z, Geramizadeh B, Bagheri Z, Karimzadeh S, Shojazadeh A. Beyzaei Z, et al. Front Immunol. 2020 Dec 23;11:613128. doi: 10.3389/fimmu.2020.613128. eCollection 2020. Front Immunol. 2020. PMID: 33424868 Free PMC article.

The studies which reported 2016 liver transplant recipients with de novo DSAs showed an increased complication risk, i.e. graft loss and chronic rejection (OR 3.61; 95% CI 1.94-6.71, P < 0.001; I(2) 58.19%), and allograft rejection alone (OR 6.43; 95% CI: 3.17-13.04;

…
The studies which reported 2016 liver transplant recipients with de novo DSAs showed an increased complication risk, i.e. graft loss and chr …
Association between polymorphisms in DNA repair genes (XRCC1 and XRCC7) and risk of preeclampsia.
Saadat I, Beyzaei Z, Aghaei F, Kamrani S, Saadat M. Saadat I, et al. Arch Gynecol Obstet. 2012 Dec;286(6):1459-62. doi: 10.1007/s00404-012-2471-7. Epub 2012 Jul 24. Arch Gynecol Obstet. 2012. PMID: 22825692
The Gln/Gln genotype of Arg399Gln XRCC1 polymorphism increased the risk of PE (OR=2.39, 95 % CI: 1.38-4.14, P=0.002). Statistical analysis revealed that the haplotype "194Arg-399Gln" showed higher frequency among PE patients compared to the controls (OR=1.65, 95% CI: 1.23- …
The Gln/Gln genotype of Arg399Gln XRCC1 polymorphism increased the risk of PE (OR=2.39, 95 % CI: 1.38-4.14, P=0.002). Statistical ana …
Expedient multicomponent synthesis of a small library of some novel highly substituted pyrido[2,3-d]pyrimidine derivatives mediated and promoted by deep eutectic solvent and in vitro and quantum mechanical study of their antibacterial and antifungal activities.
Aryan R, Beyzaei H, Nojavan M, Pirani F, Samareh Delarami H, Sanchooli M. Aryan R, et al. Mol Divers. 2019 Feb;23(1):93-105. doi: 10.1007/s11030-018-9859-7. Epub 2018 Jul 19. Mol Divers. 2019. PMID: 30027387