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Page 1
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: ghabeli h. Hum Genomics. 2024 Apr 3;18(1):35. doi: 10.1186/s40246-024-00598-5. Hum Genomics. 2024. PMID: 38570878 Free PMC article.
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: ghabeli h. 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
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: ghabeli h. 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.
The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.
Mansouri V, Heidari M, Bemanalizadeh M, Azizimalamiri R, Nafissi S, Akbari MG, Barzegar M, Moayedi AR, Badv RS, Mohamadi M, Tavasoli AR, Amirsalari S, Khajeh A, Inaloo S, Fatehi F, Hosseinpour S, Babaei M, Hosseini SA, Mahdi Hosseiny SM, Fayyazi A, Hosseini F, Toosi MB, Khosroshahi N, Ghabeli H, Biglari HN, Kakhki SK, Mirlohi SH, Bidabadi E, Mohammadi B, Omrani A, Sedighi M, Vafaee-Shahi M, Rasulinezhad M, Hoseini SM, Movahedinia M, Rezaei Z, Karimi P, Farshadmoghadam H, Anvari S, Yaghini O, Nasiri J, Zamani G, Ashrafi MR. Mansouri V, et al. Among authors: ghabeli h. J Neuromuscul Dis. 2023;10(2):211-225. doi: 10.3233/JND-221614. J Neuromuscul Dis. 2023. PMID: 36776076
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: ghabeli h. 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.
The quality of life in children with spinal muscular atrophy: a case-control study.
Zamani G, Ashrafi MR, Ghabeli H, Akbari MG, Mohammadi M, Badv RS, Hosseinpour S, Haghighi R, Pourbakhtyaran E, Khosroshahi N, Heidari M. Zamani G, et al. Among authors: ghabeli h. BMC Pediatr. 2022 Dec 12;22(1):708. doi: 10.1186/s12887-022-03751-y. BMC Pediatr. 2022. PMID: 36503502 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: ghabeli h. 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.
12 results