Behavioral and electrophysiological evidence for parent training in young children with autism symptoms and excessive screen-time H Pouretemad, R Khosrowabadi, J Fathabadi, S Nikbakht Asian journal of psychiatry 45, 7-12, 2019 | 39 | 2019 |
Renal hemosiderosis among Iranian transfusion dependent β-thalassemia major patients M Hashemieh, M Radfar, A Azarkeivan, SMTH Tabatabaei, S Nikbakht, ... International journal of hematology-oncology and stem cell research 11 (2), 133, 2017 | 36 | 2017 |
Effects of parent–child interaction training on children who are excessively exposed to digital devices: A pilot study S Sadeghi, HR Pouretemad, R Khosrowabadi, J Fathabadi, S Nikbakht The International Journal of Psychiatry in Medicine 54 (6), 408-423, 2019 | 21 | 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 | 18 | 2018 |
Parent–child interaction effects on autism symptoms and EEG relative power in young children with excessive screen-time S Sadeghi, HR Pouretemad, R Khosrowabadi, J Fathabadi, S Nikbakht Early Child Development and Care 191 (6), 827-836, 2021 | 12 | 2021 |
Impact of using digital devices on the health of children: a systematic review S Sadeghi, HR Pouretemad, R Khosrowabadi, J Fathabadi, S Nikbakht Journal of Education and Community Health 5 (2), 62-71, 2018 | 7 | 2018 |
The effectiveness of emotional diet intervention on parent-child interaction and parental stress in mothers of young children with autistic-like behaviors and exposure to … S Sadeghi, HR Pouretemad, R Khosroabadi, J Fathabadi, S Nikbakht Daneshvar Medicine 26 (4), 1-10, 2020 | 3 | 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 | 2 | 2023 |
Seizure as the early and main manifestation of infantile vanishing white matter disease: a case report N Rezaei, S Nikbakht, MR Ashrafi, Z Rezaei, N Mahdieh, H Alizadeh, ... Iranian Journal of Pediatrics 28 (2), 2018 | 2 | 2018 |
Comparative efficacy of risdiplam and nusinersen in Type 2 and 3 spinal muscular atrophy patients: A cohort study using real-world data MR Ashrafi, M Babaee, SS Hashemi Nazari, M Barzegar, M Ghazavi, ... Journal of Neuromuscular Diseases, 22143602241288087, 2024 | | 2024 |
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population N Mahdieh, M Heidari, Z Rezaei, AR Tavasoli, S Hosseinpour, ... Human genomics 18 (1), 35, 2024 | | 2024 |