| Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus S Saee-Rad, H Hashemi, M Miraftab, MR Noori-Daloii, MH Chaleshtori, ... Molecular vision 17, 3128, 2011 | 90 | 2011 |
| Analysis of superoxide dismutase 1, dual-specificity phosphatase 1, and transforming growth factor, beta 1 genes expression in keratoconic and non-keratoconic corneas S Saee-Rad, R Raoofian, M Mahbod, M Miraftab, M Mojarrad, S Asgari, ... Molecular vision 19, 2501, 2013 | 37 | 2013 |
| Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa M Beheshtian, SS Rad, M Babanejad, M Mohseni, H Hashemi, ... Archives of Iranian Medicine 18 (11), 0-0, 2015 | 30 | 2015 |
| Serum biochemistry of ostrich (Striothio camelus) in Iran ZK P Khazraiinia, S Saei, Mehrdad Mohri, HR Haddadzadeh, HR Darvisihha Comparative Clinical Pathology 15 (2), 87-89, 2006 | 22 | 2006 |
| Lack of association between the C677T single nucleotide polymorphism of the MTHFR gene and glaucoma in Iranian patients N Nilforoushan, S Aghapour, R Raoofian, SS Rad, WK Greene, ... Acta Medica Iranica, 208-212, 2012 | 19 | 2012 |
| Mutation screening in the mitochondrial D-loop region of tumoral and non-tumoral breast cancer in Iranian patients B Rahmani, C Azimi, R Omranipour, R Raoofian, K Zendehdel, ... Acta Medica Iranica, 447-453, 2012 | 18 | 2012 |
| Differential BMI1, TWIST1, SNAI2 mRNA expression pattern correlation with malignancy type in a spectrum of common cutaneous malignancies and melanoma Differential BMI1, TWIST1, SNAI2 mRNA expression pattern ... Clinical and Translational Oncology 19 (4), 489–497, 2016 | 10* | 2016 |
| Evaluation of the effects of magnesium sulfate on prevention of post-dural-puncture headache in elective cesarean in Kamali hospital B Mashak, SM Pouryaghobi, M Rezaee, SS Rad, M Ataei, A Borzabadi Electronic Journal of General Medicine 17 (3), 2020 | 8 | 2020 |
| Differential expression of human homeodomain TGIFLX in brain tumor cell lines R Raoofian, MR Noori-Daloii, S Saee-Rad, MH Modarresi, SH Ghaffari, ... Acta Medica Iranica, 834-841, 2013 | 8 | 2013 |
| EVALUATING THE MOST COMMON MUTATION IN BRCAI AND BRCA2 GENES IN WOMEN WHO HAD MOTHERS WITH BREST CANCER AND CONTROLS AKS SARVAR FAEZEH, NEKOUIAN REZA, SAEI RAD SAMIRA, GHARAVI MOHAMMAD JAVAD ... JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES 26 (141), 137-142, 2016 | 3 | 2016 |
| Oropharyngeal colonization of Haemophilus influenzae type b and serologic response after administration of third dose of pentavalent vaccine to 12-month-old children in Karaj … F Shirvani, R Arjmand, M Golami, EN Tavana, SS Rad, K Pourrostami, ... Archives of Pediatric Infectious Diseases 7 (1), 2019 | 2 | 2019 |
| Balanced reciprocal translocation in a case of recurrent miscarriage SS masoumeh farahani Alborz university medical Journal 10 (2), 133-136, 2021 | | 2021 |
| KIR3DL1 gene genotype in patients with spontaneous recurrent abortion M Ataei, M Mirzaei, F Inanloo, N Maleki, SS Rad, SM Noorbakhsh, ... Archivos Venezolanos de Farmacología y Terapéutica 40 (2), 121-128, 2021 | | 2021 |
| Genetic evaluation of thrombophilia panel in recurrent miscarriage at Karami Hospital of Karaj M Ataei, M Hedayat, SS Rad, J Rezaei, NJ Namini, B Mashak International Journal of Psychosocial Rehabilitation 24 (3), 1398-1406, 2020 | | 2020 |
| Investigation of new chromosomal abnormalities associated with recurrent abortion M Ataei, Z Moslehi, R Rezapour-Nasrabad, M Modoodi, P Farahbakhsh, ... International Journal of Psychosocial Rehabilitation 24 (7), 61-68, 2020 | | 2020 |
| MUTATION SCREENING OF ENAM, KLK4, MMP20 AND FAM83HGENES AMONG THE MEMBERS OF FIVE IRANIAN FAMILIES AFFECTED WITH AUTOSOMAL RECESSIVE HYPOPLASTIC AMELOGENESIS IMPERFECTA HM GHANDEHARI MOTLAGH M., MOHANDES F., NOORI DALOII H., AZIMI C., NOORI ... JOURNAL OF SCIENCES ISLAMIC REPUBLIC OF IRAN 22 (4), 305-310, 2011 | | 2011 |
| Molecular Investigation of Brugada Syndrome Prevalence in Iranian Families samira saee rad | | |
mohammad miraftabophthalmologist,Cornea & Refractive surgeonVerified email at noorvision.com
