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Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.
Suri F, Narooie-Nejad M, Safari I, Moazzeni H, Rohani MR, Khajeh A, Klotzle B, Fan JB, Elahi E. Suri F, et al. Among authors: khajeh a. J Neurol Sci. 2014 Dec 15;347(1-2):305-9. doi: 10.1016/j.jns.2014.10.031. Epub 2014 Oct 22. J Neurol Sci. 2014. PMID: 25455305
Prevalence of G6PD deficiency in Children with Hepatitis A.
Miri-Aliabad G, Khajeh A, Shahraki T. Miri-Aliabad G, et al. Among authors: khajeh a. Int J Hematol Oncol Stem Cell Res. 2017 Apr 1;11(2):92-95. Int J Hematol Oncol Stem Cell Res. 2017. PMID: 28875002 Free PMC article.
Molecular genetic study of Calpainopathy in Iran.
Mojbafan M, Khajeh A, Habibi H, Bagherian H, Zeinali S. Mojbafan M, et al. Among authors: khajeh a. Gene. 2018 Nov 30;677:259-265. doi: 10.1016/j.gene.2018.07.067. Epub 2018 Jul 27. Gene. 2018. PMID: 30056071
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: khajeh a. Neurogenetics. 2023 Oct;24(4):279-289. doi: 10.1007/s10048-023-00730-y. Epub 2023 Aug 19. Neurogenetics. 2023. PMID: 37597066
57 results