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A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies.
Hosseinpour S, Razmara E, Heidari M, Rezaei Z, Ashrafi MR, Dehnavi AZ, Kameli R, Bereshneh AH, Vahidnezhad H, Azizimalamiri R, Zamani Z, Pak N, Rasulinezhad M, Mohammadi B, Ghabeli H, Ghafouri M, Mohammadi M, Zamani GR, Badv RS, Saket S, Rabbani B, Mahdieh N, Ahani A, Garshasbi M, Tavasoli AR. Hosseinpour S, et al. Among authors: saket s. Brain Dev. 2024 Apr;46(4):167-179. doi: 10.1016/j.braindev.2023.12.003. Epub 2023 Dec 21. Brain Dev. 2024. PMID: 38129218
Incidence of Pediatric Multiple Sclerosis in Iran within 2000-2019.
Nasehi MM, Nikkhah A, Moosazadeh M, Saket S, Alizadeh Navaei R. Nasehi MM, et al. Among authors: saket s. Iran J Child Neurol. 2022 Winter;16(1):31-38. doi: 10.22037/ijcn.v16i1.35572. Epub 2022 Jan 1. Iran J Child Neurol. 2022. PMID: 35222655 Free PMC article.
19 results