| 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 | 84 | 2020 |
| The effects of classic ketogenic diet on serum lipid profile in children with refractory seizures GR Zamani, M Mohammadi, MR Ashrafi, P Karimi, M Mahmoudi, RS Badv, ... Acta Neurologica Belgica 116, 529-534, 2016 | 72 | 2016 |
| Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management MR Ashrafi, AR Tavasoli Brain and Development 39 (5), 369-385, 2017 | 49 | 2017 |
| Efficacy and safety of cinnarizine in the prophylaxis of migraine in children: a double-blind placebo-controlled randomized trial MR Ashrafi, S Salehi, RA Malamiri, M Heidari, SA Hosseini, M Samiei, ... Pediatric Neurology 51 (4), 503-508, 2014 | 49 | 2014 |
| Effects of miglustat on stabilization of neurological disorder in Niemann–Pick disease type C: Iranian pediatric case series P Karimzadeh, SH Tonekaboni, MR Ashrafi, Y Shafeghati, A Rezayi, ... Journal of Child Neurology 28 (12), 1599-1606, 2013 | 32 | 2013 |
| Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical … M Amanat, A Majmaa, M Zarrabi, M Nouri, MG Akbari, AR Moaiedi, ... Stem Cell Research & Therapy 12, 1-15, 2021 | 29 | 2021 |
| Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report H Aryan, E Razmara, D Farhud, M Zarif-Yeganeh, S Zokaei, SA Hassani, ... BMC neurology 20, 1-11, 2020 | 28 | 2020 |
| Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants N Mahdieh, M Soveizi, AR Tavasoli, A Rabbani, MR Ashrafi, ... Scientific reports 11 (1), 3231, 2021 | 24 | 2021 |
| Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability E Heidari, A Caddeo, K Zarabadi, M Masoudi, AR Tavasoli, S Romeo, ... Genomics 112 (6), 4072-4077, 2020 | 23 | 2020 |
| Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trial M Amanat, M Togha, E Agah, M Ramezani, AR Tavasoli, R Azizi Malamiri, ... Cephalalgia 40 (7), 665-674, 2020 | 23 | 2020 |
| Coronavirus, its neurologic manifestations, and complications MR Ashrafi, R Azizimalamiri, RS Badv, AR Tavasoli, A Nikkhah, ... Iranian Journal of Pediatrics 30 (2), 1-4, 2020 | 23 | 2020 |
| Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations AR Tavasoli, N Parvaneh, MR Ashrafi, Z Rezaei, J Zschocke, P Rostami Orphanet Journal of Rare Diseases 13, 1-8, 2018 | 23 | 2018 |
| Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review P Rostami, S Hosseinpour, MR Ashrafi, H Alizadeh, M Garshasbi, ... Acta Neurologica Belgica 120, 511-516, 2020 | 19 | 2020 |
| Levetiracetam for prophylactic treatment of pediatric migraine: A randomized double-blind placebo-controlled trial H Montazerlotfelahi, M Amanat, AR Tavasoli, E Agah, GR Zamani, ... Cephalalgia 39 (12), 1509-1517, 2019 | 19 | 2019 |
| 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 | 18 | 2019 |
| The first report of relative incidence of inherited white matter disorders in an Asian country based on an Iranian bioregistry system MR Ashrafi, Z Rezaei, M Heidari, S Nikbakht, RA Malamiri, M Mohammadi, ... Journal of Child Neurology 33 (4), 255-259, 2018 | 17 | 2018 |
| Alexander disease: report of two unrelated infantile form cases, identified by GFAP mutation analysis and review of literature; the first report from Iran MR Ashrafi, A Tavasoli, O Aryani, H Alizadeh, M Houshmand Iranian Journal of Pediatrics 23 (4), 481, 2013 | 17 | 2013 |
| Novel neuroclinical findings of autosomal recessive primary microcephaly 15 in a consanguineous Iranian family E Razmara, H Azimi, AR Tavasoli, E Fallahi, SV Sheida, M Eidi, A Bitaraf, ... European Journal of Medical Genetics 63 (12), 104096, 2020 | 15 | 2020 |
| Alexander disease: a leukodystrophy that may mimic brain tumor A Tavasoli, T Armangue, CY Ho, M Whitehead, M Bornhorst, J Rhee, ... Journal of child neurology 32 (2), 184-187, 2017 | 15 | 2017 |
| Mutation update: The spectra of PLEC sequence variants and related plectinopathies H Vahidnezhad, L Youssefian, N Harvey, AR Tavasoli, AH Saeidian, ... Human mutation 43 (12), 1706-1731, 2022 | 13 | 2022 |
Masoud GarshasbiAssociate Professor of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares UniversityEmail verificata su modares.ac.ir