| An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies MR Ashrafi, M Amanat, M Garshasbi, R Kameli, Y Nilipour, M Heidari, ... Expert review of neurotherapeutics 20 (1), 65-84, 2020 | 70 | 2020 |
| RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant R Kameli, M Amanat, Z Rezaei, S Hosseionpour, S Nikbakht, H Alizadeh, ... Orphanet Journal of Rare Diseases 14, 1-7, 2019 | 16 | 2019 |
| Analysis of the association Hind III Polymorphism of Lipoprotein Lipase gene on the risk of coronary artery disease M Imeni, M Hasanzad, T Naji, B Poopak, M Babanejad, HR Sanati, ... Research in Molecular Medicine 1 (3), 18-23, 2013 | 8 | 2013 |
| Leukoencephalopathy in RIN2 syndrome: novel mutation and expansion of clinical spectrum R Kameli, MR Ashrafi, F Ehya, H Alizadeh, S Hosseinpour, M Garshasbi, ... European Journal of Medical Genetics 63 (1), 103629, 2020 | 6 | 2020 |
| High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry M Ashrafi, R Kameli, S Hosseinpour, E Razmara, Z Zamani, Z Rezaei, ... neurogenetics 24 (4), 279-289, 2023 | 1 | 2023 |
| Association between cytochrome P450 2 C9 and vitamin K epoxide reductase complex subunit 1 polymorphisms with warfarin dose among Iranian patients R Kameli, M Hasanzad, Z Tahmasebi Fard, M Babanejad, M Imeni, ... Research in Molecular Medicine 4 (4), 38-44, 2016 | 1 | 2016 |
| A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies S Hosseinpour, E Razmara, M Heidari, Z Rezaei, MR Ashrafi, AZ Dehnavi, ... Brain and Development 46 (4), 167-179, 2024 | | 2024 |
| High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry (Aug, 10.1007/s10048-023-00730-y, 2023) M Ashrafi, R Kameli, S Hosseinpour, E Razmara, Z Zamani, Z Rezaei, ... Neurogenetics 24 (4), 317-318, 2023 | | 2023 |
| An Asymptomatic Case of Megalencephalic Leukoencephalopathy with Subcortical Cysts R Kameli, M Barzegar, H Alizadeh, MR Ashrafi, S Sadeghvand, Z Rezaei, ... Iranian Journal of Pediatrics 29 (4), 2019 | | 2019 |
| Beta-Ketothiolase Deficiency as A Treatable Neurometabolic Disorder: A Case Report Due to A Novel Compound Heterozygote Mutations in ACAT1 Gene P Rostami, R Mohsenipour, R Kameli, MR Ashrafi, AR Tavasoli, ... Biomedical Journal of Scientific & Technical Research 15 (3), 1-4, 2019 | | 2019 |
