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Page 1
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: mohammadi m. 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: mohammadi m. 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.
Local treatment in metastatic GIST patients: A multicentre analysis from the Dutch GIST Registry.
Brink P, Kalisvaart GM, Schrage YM, Mohammadi M, Ijzerman NS, Bleckman RF, Wal T, de Geus-Oei LF, Hartgrink HH, Grunhagen DJ, Verhoef C, Sleijfer S, Oosten AW, Been LB, van Ginkel RJ, Reyners AKL, Bonenkamp HJ, Desar IME, Gelderblom H, van Houdt WJ, Steeghs N, Fiocco M, van der Hage JA. Brink P, et al. Among authors: mohammadi m. Eur J Surg Oncol. 2023 Sep;49(9):106942. doi: 10.1016/j.ejso.2023.05.017. Epub 2023 May 23. Eur J Surg Oncol. 2023. PMID: 37246093 Free 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: mohammadi m. 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
53 results