Items where Author is "Bagheri, N."

(2022) Population-level risks of alcohol consumption by amount, geography, age, sex, and year: a systematic analysis for the Global Burden of Disease Study 2020. LANCET. pp. 185-235. ISSN 0140-6736 1474-547X J9 - LANCET

(2022) Sensitivity Analysis with the Monte Carlo Method and Prediction of Atenolol Removal Using Modified Multiwalled Carbon Nanotubes Based on the Response Surface Method: Isotherm and Kinetics Studies. INTERNATIONAL JOURNAL OF CHEMICAL ENGINEERING. ISSN 1687-806X 1687-8078 J9 - INT J CHEM ENG

(2022) The favorable impacts of silibinin polyphenols as adjunctive therapy in reducing the complications of COVID-19: A review of research evidence and underlying mechanisms. Biomed Pharmacother. p. 113593. ISSN 0753-3322 (Print) 0753-3322

(2019) Effectiveness of Emotion Regulation Group Therapy on Craving, Emotion Problems, and Marital Satisfaction in Patients with Substance Use Disorders: A Randomized Clinical Trial. Iran J Psychiatry. pp. 283-290. ISSN 1735-4587 (Print) 1735-4587 (Linking)

(2019) Motor network recovery and chronic spinal cord compression. Journal of Neurosurgery-Spine. p. 453. ISSN 1547-5654

(2016) Acute and chronic tramadol administration impair spatial memory in rat. Research in Pharmaceutical Sciences. pp. 49-57. ISSN 1735-5362

(2015) Comparative Immune Response in Children and Adults with H. pylori Infection. Journal of Immunology Research. ISSN 2314-8861

(2015) Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. Jundishapur Journal of Microbiology. ISSN 2008-3645

(2015) Frequency of virulence factors in Helicobacter pylori-infected patients with gastritis. Microbial Pathogenesis. pp. 67-72. ISSN 0882-4010

(2015) New insight to IL-23/IL-17 axis in Iranian infected adult patients with gastritis : effects of genes polymorphisms on expression of cytokines. Acta Gastro-Enterologica Belgica. pp. 212-218. ISSN 0001-5644

(2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. International Journal of Audiology. pp. 124-130. ISSN 1499-2027