| MEFV mutations in Iranian Azeri Turkish patients with familial Mediterranean fever M Bonyadi, M Esmaeili, H Jalali, MH Somi, A Ghaffari, M Rafeey, K Sakha, ... Clinical genetics 76 (5), 477-480, 2009 | 48 | 2009 |
| Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β‐Thalassemia Major: A Comprehensive Review in 2015 H Darvishi Khezri, E Salehifar, M Kosaryan, A Aliasgharian, H Jalali, ... Advances in Pharmacological and Pharmaceutical Sciences 2016 (1), 3046373, 2016 | 40 | 2016 |
| Evaluation of adverse effects of chemotherapy regimens of 5-fluoropyrimidines derivatives and their association with DPYD polymorphisms in colorectal cancer patients R Negarandeh, E Salehifar, F Saghafi, H Jalali, G Janbabaei, ... BMC cancer 20, 1-7, 2020 | 32 | 2020 |
| Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis M Zafari, M Kosaryan, P Gill, A Alipour, M Shiran, H Jalalli, A Banihashemi, ... Annals of hematology 95, 1341-1350, 2016 | 31 | 2016 |
| Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012 H Jalali, MR Mahdavi, P Roshan, M Kosaryan, H Karami, M Mahdavi Hematology 19 (4), 192-195, 2014 | 26 | 2014 |
| Is Vitamin C Supplementation in Patients with β-Thalassemia Major Beneficial or Detrimental? HJ Hadi Darvishi Khezri, Amir Emami Zeydi, Hassan Sharifi Hemoglobin 40 (4), 293-294, 2016 | 22 | 2016 |
| Detection of rare beta globin gene mutation [+ 22 5UTR (G> A)] in an infant, despite prenatal screening MR Mahdavi, H Karami, MT Akbari, H Jalali, P Roshan Case Reports in Hematology 2013 (1), 906292, 2013 | 21 | 2013 |
| Investigation of five common mutations on phenylalanine hydroxylase gene of phenylketonuria patients from two provinces in north of Iran D Zamanfar, H Jalali, MR Mahdavi, M Maadanisani, H Zaeri, E Asadpoor International Journal of Preventive Medicine 8 (1), 89, 2017 | 20 | 2017 |
| Why does the Iranian national program of screening newborns for G6PD enzyme deficiency miss a large number of affected infants? M Kosaryan, MR Mahdavi, H Jalali, P Roshan Pediatric hematology and oncology 31 (1), 95-100, 2014 | 17 | 2014 |
| Torque Teno Virus (TTV) among β-thalassemia and haemodialysis patients in Mazandaran Province (North of Iran) H Jalali, MR Mahdavi, N Zaeromali International journal of molecular and cellular medicine 6 (1), 56, 2017 | 16 | 2017 |
| β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran province, Iran MR Mahdavi, H Jalali, M Kosaryan, P Roshan, M Mahdavi Genes & genetic systems 90 (1), 55-57, 2015 | 15 | 2015 |
| Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran F Aghajani, MR Mahdavi, M Kosaryan, M Mahdavi, M Hamidi, H Jalali Genes & genetic systems 91 (6), 311-313, 2016 | 14 | 2016 |
| Evaluation of gene mutations involved in drug resistance in Mycobacterium tuberculosis strains derived from tuberculosis patients in Mazandaran, Iran, 2013 F Babamahmoodi, MR Mahdavi, H Jalali, B Talebi, P Roshan, M Mahdavi International journal of molecular and cellular medicine 3 (3), 190, 2014 | 14 | 2014 |
| Is quantitative HBsAg measurement a reliable substitute for HBV DNA quantitation? MR Mahdavi, MR Haghshenas, P Roshan, MT Hojjati, M Mahdavi, ... Research in Molecular Medicine 3 (3), 33-37, 2015 | 9 | 2015 |
| Frequency of Factor V Leiden, Prothrombin G20210 and C667T Mutations in Methylenetetrahydrofolate Reductase in Patients with Beta and Intermediate Thalassemia Compared with … H Soteh, A Aliasgharian, H Jalali, SN Nejati Fard, M Kosarian, H Karami Journal of Mazandaran University of Medical Sciences 21 (81), 2-9, 2011 | 4 | 2011 |
| First report of c. 425-1G> A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia H Jalali, M Najafi, A Khoshaeen, MR Mahdavi, M Mahdavi European Journal of Ophthalmology 31 (5), NP23-NP26, 2021 | 3 | 2021 |
| A report of Hb Fontainebleau [α21 (B2) Ala> Pro] as a result of founder effect phenomenon H Jalali, ST Rasouli, M Najafi, H Karami, MR Mahdavi, M Mahdavi Gene Reports 19, 100587, 2020 | 3 | 2020 |
| First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy H Jalali, A Khoshaeen, MR Mahdavi, M Mahdavi Clinical Case Reports 10 (8), e6203, 2022 | 2 | 2022 |
| Dihydropyrimidine dehydrogenase gene variation and its association with 5-fluorouracil toxicity in colorectal patients E Salehifar, MJ Abd Haghighi, R Negarandeh, G Janbabai, F Safgafi, ... Asian Pacific Journal of Cancer Biology 3 (3), 65-69, 2018 | 2 | 2018 |
| Comparison of fluorescent spot test, decolorization test and quantitative enzyme assay in detection of G6PD enzyme deficiency M Kosaryan, MR Mahdavi, H Jalali, P Roshan Journal of Gorgan University of Medical Sciences 17 (3), 108-113, 2015 | 2 | 2015 |
Dr. Mohammadreza Mahdavi AmiriMazandaran University of Medical Sciences, Iran在 fajrlaboratory.com 的电子邮件经过验证
