| Primary and secondary microcephaly, global developmental delay, and seizure in two siblings caused by a novel missense variant in the ZNF335 gene AR Tavasoli, EHE Memar, MR Ashrafi, SMM Hosseini, R Haghighi, ... Journal of Molecular Neuroscience 72 (4), 719-729, 2022 | 8 | 2022 |
| Childhood Guillain–Barre syndrome in the SARS‐CoV‐2 era: Is there any causative relation? E Pourbakhtyaran, M Heidari, MG Akbari, M Mohammadi, RS Badv, ... Clinical Case Reports 10 (12), e6772, 2022 | 5 | 2022 |
| Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly H Aryan, S Zokaei, D Farhud, M Keykhaei, MR Ashrafi, M Rasulinezhad, ... Irish Journal of Medical Science (1971-), 1-9, 2022 | 2 | 2022 |
| Nonsyndromic early-onset epileptic encephalopathies: two novel KCTD7 pathogenic variants and a literature review S Binaafar, M Garshasbi, AR Tavasoli, RS Badv, SMM Hosseiny, ... Developmental Neuroscience 43 (6), 348-357, 2021 | 2 | 2021 |
| 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 |
| Genetic analysis of forty MLPA-negative Duchenne muscular dystrophy patients by whole-exome sequencing GR Zamani, MF Mohammadi, AR Tavasoli, MR Ashrafi, S Hosseinpour, ... Journal of Molecular Neuroscience 72 (5), 1098-1107, 2022 | 1 | 2022 |
| Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study MR Ashrafi, E Pourbakhtyaran, M Rohani, B Shalbafan, AR Tavasoli, ... Clinical Case Reports 10 (4), e05777, 2022 | 1 | 2022 |
| ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants AZ Dehnavi, E Heidari, M Rasulinezhad, M Heidari, MR Ashrafi, ... Human Genomics 15, 1-11, 2021 | 1 | 2021 |
| 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), 1-18, 2024 | | 2024 |
| Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study EHE Memar, M Heidari, H Ghabeli, E Pourbakhtyaran, R Haghighi, ... Archives of Iranian medicine 26 (3), 166, 2023 | | 2023 |
| Childhood Guillain-Barre´ syndrome in the SARS-CoV-2 Era: Is there any causative relation?(preprint) E Pourbakhtyaran, M Heidari, MG Akbar, M Mohammadi, RS Badv, ... | | 2022 |
| Treatable Ataxia: a comprehensive case series study M reza Ashrafi, E Pourbakhtyaran, M Rohani, B Shalbafan, AR Tavasoli, ... Authorea Preprints, 2021 | | 2021 |
| Incidence and common locations of Mongolian spots in newborns: a university hospital MR Ashrafi, F Ghanjizadeh, SM Hosseiny, SAN SA, H Shajari, S Zandieh مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 65, 1-2, 2007 | | 2007 |
