| Comparative measurement of ghrelin, leptin, adiponectin, EGF and IGF-1 in breast milk of mothers with overweight/obese and normal-weight infants A Khodabakhshi, M Ghayour-Mobarhan, H Rooki, R Vakili, SI Hashemy, ... European journal of clinical nutrition 69 (5), 614-618, 2015 | 81 | 2015 |
| Folate targeted PEGylated liposomes for the oral delivery of insulin: In vitro and in vivo studies JR Yazdi, M Tafaghodi, K Sadri, M Mashreghi, AR Nikpoor, ... Colloids and Surfaces B: Biointerfaces 194, 111203, 2020 | 62 | 2020 |
| Effects of zinc supplementation in occurrence and duration of common cold in school aged children during cold season: a double-blind placebo-controlled trial R Vakili, M Vahedian, GHH KHODAEI, M Mahmoudi Iranian Journal of Pediatrics 19 (4), 376-380, 2009 | 45 | 2009 |
| Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran T Hamzehloei, SA Hosseini, R Vakili, M Mojarad Gene 506 (1), 230-232, 2012 | 35 | 2012 |
| Investigation of the effect of high dairy diet on body mass index and body fat in overweight and obese children M Ghayour-Mobarhan, A Sahebkar, R Vakili, M Safarian, M Nematy, ... The Indian Journal of Pediatrics 76, 1145-1150, 2009 | 32 | 2009 |
| Three novel CYP21A2 mutations and their protein modelling in patients with classical 21‐hydroxylase deficiency from northeastern Iran A Baradaran‐Heravi, R Vakili, T Robins, J Carlsson, N Ghaemi, A A’rabi, ... Clinical endocrinology 67 (3), 335-341, 2007 | 25 | 2007 |
| Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran R Vakili, A Baradaran-Heravi, B Barid-Fatehi, M Gholamin, N Ghaemi, ... Hormone research 63 (3), 119-124, 2005 | 24 | 2005 |
| Impact of intravenous trehalose administration in patients with niemann–pick disease types A and B M Mobini, S Radbakhsh, F Kubaski, P Eshraghi, S Vakili, R Vakili, ... Journal of Clinical Medicine 11 (1), 247, 2022 | 21 | 2022 |
| Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing A Tafazoli, P Eshraghi, F Pantaleoni, R Vakili, M Moghaddassian, ... Advances in medical sciences 63 (1), 87-93, 2018 | 21 | 2018 |
| The genetic spectrum of familial hypercholesterolemia (FH) in the Iranian population RH Fairoozy, M Futema, R Vakili, MR Abbaszadegan, S Hosseini, ... Scientific reports 7 (1), 17087, 2017 | 21 | 2017 |
| The effect of Ramadan fasting on thyroid hormones in 9-13 years old pre-menarche girls S Bahrayni, R Vakili, M Nematy, A Norouzy, SI Hashemy, M Ebrahimi, ... J Fasting Health 1 (2), 46-52, 2013 | 20 | 2013 |
| Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients MR Abbaszadegan, S Hassani, R Vakili, MR Saberi, A Baradaran-Heravi, ... Endocrine 44, 212-219, 2013 | 20 | 2013 |
| The effect of zinc supplementation on linear growth and growth factors in primary schoolchildren in the suburbs Mashhad, Iran R Vakili, M Yazdan Bakhsh, M Vahedian, M Mahmoudi, M Saeidi, S Vakili Journal of Pediatric Perspectives 3 (2.1), 1-7, 2015 | 19 | 2015 |
| The association between carotid intima-media thickness and the duration of type 1 diabetes in children MP Rad, D Farrokh, R Vakili, M Omidbakhsh, M Mohammadi Iranian Journal of Pediatrics 24 (3), 249, 2014 | 19 | 2014 |
| Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of< 5 years in the Iranian population H Yaghootkar, F Abbasi, N Ghaemi, A Rabbani, MN Wakeling, P Eshraghi, ... Diabetic Medicine 36 (12), 1694-1702, 2019 | 18 | 2019 |
| Novel DNA variation of GPR54 gene in familial central precocious puberty N Ghaemi, M Ghahraman, S Noroozi Asl, R Vakili, F Fardi Golyan, ... Italian Journal of Pediatrics 45, 1-6, 2019 | 17 | 2019 |
| CASE REPORT: PRECOCIOUS PUBERTY: AN UNUSUAL PRESENTATION OF HYPOTHYROIDISM N Ghaemi, R Vakili, S Bagheri INTERNATIONAL JOURNAL OF PEDIATRICS 1 (21), 51-54, 2013 | 17 | 2013 |
| Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes SN Asl, R Vakili, S Vakili, F Soheilipour, M Hashemipour, S Ghahramani, ... Journal of Pediatric Endocrinology and Metabolism 32 (6), 607-613, 2019 | 16 | 2019 |
| Mutations in HNF1A gene are not a common cause of familial young-onset diabetes in Iran M Moghbeli, B Naghibzadeh, M Ghahraman, S Fatemi, M Taghavi, ... Indian Journal of Clinical Biochemistry 33, 91-95, 2018 | 13 | 2018 |
| Evaluation of umbilical cord vitamin D level and maternal factors effective on it in three hospitals of Emam Reza, Ghaem & Omol Banin during 2013-2014 F Akhlaghi, R Vakili, E Khorasani The Iranian Journal of Obstetrics, Gynecology and Infertility 17 (134), 1-7, 2015 | 13 | 2015 |
nosrat ghaemiassociated professor of medical science,mashhad universityGeverifieerd e-mailadres voor mums.ac.ir