| Clinical spectrum in multiple families with primary COQ10 deficiency SS Hashemi, D Zare‐Abdollahi, MK Bakhshandeh, A Vafaee, ... American Journal of Medical Genetics Part A 185 (2), 440-452, 2021 | 19 | 2021 |
| Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations M Khani, H Shamshiri, F Fatehi, M Rohani, B Haghi Ashtiani, ... Molecular Genetics & Genomic Medicine 8 (7), e1240, 2020 | 10 | 2020 |
| Anticipation can be more common in hereditary spastic paraplegia with SPAST mutations than it appears SS Hashemi, R Hajati, A Davarzani, M Rohani, F DanaeeFard, ... Canadian Journal of Neurological Sciences 49 (5), 651-661, 2022 | 8 | 2022 |
| The second family affected with a PRDM8-related disease A Davarzani, A Shahrokhi, SS Hashemi, A Ghasemi, ... Neurological Sciences, 1-9, 2022 | 7 | 2022 |
| Dysregulation of miRNA expression in patients with chronic myelogenous leukemia at diagnosis: a systematic review M Parsa-Kondelaji, M Musavi, F Barzegar, N Abbasian, M Rostami, ... Biomarkers in Medicine 17 (24), 1021-1029, 2023 | | 2023 |
| Genetic analysis of 50 unrelated cases affected with hereditary spastic paraplegia (HSP): a novel candidate gene R Hajati, A Davarzani, S Hashemi, MR Bidgoli, LJ Parast, M Pashaei, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 432-432, 2020 | | 2020 |
