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The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.
Mahdieh N, Heidari M, Rezaei Z, Tavasoli AR, Hosseinpour S, Rasulinejad M, Dehnavi AZ, Ghahvechi Akbari M, Badv RS, Vafaei E, Mohebbi A, Mohammadi P, Hosseiny SMM, Azizimalamiri R, Nikkhah A, Pourbakhtyaran E, Rohani M, Khanbanha N, Nikbakht S, Movahedinia M, Karimi P, Ghabeli H, Hosseini SA, Rashidi FS, Garshasbi M, Kashani MR, Ghiasvand NM, Zuchner S, Synofzik M, Ashrafi MR. Mahdieh N, et al. Among authors: hosseiny smm. Hum Genomics. 2024 Apr 3;18(1):35. doi: 10.1186/s40246-024-00598-5. Hum Genomics. 2024. PMID: 38570878 Free PMC article.
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Ashrafi M, Kameli R, Hosseinpour S, Razmara E, Zamani Z, Rezaei Z, Mashayekhi R, Pak N, Barzegar M, Azizimalamiri R, Kashani MR, Khosroshahi N, Rasulinezhad M, Heidari M, Amanat M, Abdi A, Mohammadi B, Mohammadi M, Zamani GR, Badv RS, Omrani A, Nikbakht S, Bereshneh AH, Movahedinia M, Moghaddam HF, Ardakani HS, Akbari MG, Tousi MB, Shahi MV, Hosseini F, Amouzadeh MH, Hosseini SA, Nikkhah A, Khajeh A, Alizadeh H, Yarali B, Rohani M, Karimi P, Elahi HML, Hosseiny SMM, Sadeghzadeh MS, Mohebbi H, Moghadam MH, Aryan H, Vahidnezhad H, Soveizi M, Rabbani B, Rabbani A, Mahdieh N, Garshasbi M, Tavasoli AR. Ashrafi M, et al. Among authors: hosseiny smm. Neurogenetics. 2023 Oct;24(4):317-318. doi: 10.1007/s10048-023-00733-9. Neurogenetics. 2023. PMID: 37668767 No abstract available.
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Ashrafi M, Kameli R, Hosseinpour S, Razmara E, Zamani Z, Rezaei Z, Mashayekhi R, Pak N, Barzegar M, Azizimalamiri R, Kashani MR, Khosroshahi N, Rasulinezhad M, Heidari M, Amanat M, Abdi A, Mohammadi B, Mohammadi M, Zamani GR, Badv RS, Omrani A, Nikbakht S, Bereshneh AH, Movahedinia M, Moghaddam HF, Ardakani HS, Akbari MG, Tousi MB, Shahi MV, Hosseini F, Amouzadeh MH, Hosseini SA, Nikkhah A, Khajeh A, Alizadeh H, Yarali B, Rohani M, Karimi P, Elahi HML, Hosseiny SMM, Sadeghzadeh MS, Mohebbi H, Moghadam MH, Aryan H, Vahidnezhad H, Soveizi M, Rabbani B, Rabbani A, Mahdieh N, Garshasbi M, Tavasoli AR. Ashrafi M, et al. Among authors: hosseiny smm. Neurogenetics. 2023 Oct;24(4):279-289. doi: 10.1007/s10048-023-00730-y. Epub 2023 Aug 19. Neurogenetics. 2023. PMID: 37597066
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study.
Haji Esmaeil Memar E, Heidari M, Ghabeli H, Pourbakhtyaran E, Haghighi R, Hosseiny SMM, Mamishi S, Mahmoudi S, Eshaghi H, Tavasoli AR, Mohammadi M, Shervin Badv R, Zamani G, Ghahvehchi Akbari M, Yarali B, Shirzadi R, Mohammadpour M, Yaghmaei B, Sharifzadeh Ekbatani M, Najafi Z, Ashrafi MR. Haji Esmaeil Memar E, et al. Among authors: hosseiny smm. Arch Iran Med. 2023 Mar 1;26(3):166-171. doi: 10.34172/aim.2023.25. Arch Iran Med. 2023. PMID: 37543939 Free PMC article.
Childhood Guillain-Barre syndrome in the SARS-CoV-2 era: Is there any causative relation?
Pourbakhtyaran E, Heidari M, Akbari MG, Mohammadi M, Badv RS, Zamani G, Tavasoli AR, Rezaei Z, Mamishi S, Haji Esmaeil Memar E, Hosseiny SMM, Ghabeli H, Haghighi R, Ashrafi MR. Pourbakhtyaran E, et al. Among authors: hosseiny smm. Clin Case Rep. 2022 Dec 20;10(12):e6772. doi: 10.1002/ccr3.6772. eCollection 2022 Dec. Clin Case Rep. 2022. PMID: 36545550 Free PMC article.
Follow-up of 25 patients with treatable ataxia: A comprehensive case series study.
Ashrafi MR, Pourbakhtyaran E, Rohani M, Shalbafan B, Tavasoli AR, Hosseinpour S, Rasulinezhad M, Rezaei Z, Zare Dehnavi A, Hosseiny SMM, Haghighi R, Ghabeli H, Heidari M. Ashrafi MR, et al. Among authors: hosseiny smm. Clin Case Rep. 2022 Apr 20;10(4):e05777. doi: 10.1002/ccr3.5777. eCollection 2022 Apr. Clin Case Rep. 2022. PMID: 35474986 Free PMC article.
13 results