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Page 1
Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran.
Asgarian S, Lanjanian H, Rahimipour Anaraki S, Hadaegh F, Moazzam-Jazi M, Najd-Hassan-Bonab L, Masjoudi S, Zahedi AS, Zarkesh M, Shalbafan B, Akbarzadeh M, Tehrani Fateh S, Khalili D, Momenan A, Sarbazi N, Hedayati M, Azizi F, Daneshpour MS. Asgarian S, et al. Among authors: tehrani fateh s. Sci Rep. 2024 Aug 27;14(1):19860. doi: 10.1038/s41598-024-70864-y. Sci Rep. 2024. PMID: 39191897 Free PMC article.
Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant.
Mohammadi MF, Tehrani Fateh S, Ganji M, Mohammadi P, Bahrami T, Ashrafi MR, Hosseinpour S, Heidari M, Garshasbi M, Tavasoli AR. Mohammadi MF, et al. Among authors: tehrani fateh s. Acta Neurol Belg. 2024 Aug 15. doi: 10.1007/s13760-024-02611-z. Online ahead of print. Acta Neurol Belg. 2024. PMID: 39147996
Covid-19 in Parkinson's Disease treated by drugs or brain stimulation.
Salari M, Etemadifar M, Zali A, Aminzade Z, Navalpotro-Gomez I, Tehrani Fateh S. Salari M, et al. Among authors: tehrani fateh s. Neurologia (Engl Ed). 2024 Apr;39(3):254-260. doi: 10.1016/j.nrleng.2021.07.005. Neurologia (Engl Ed). 2024. PMID: 38553103 Free article.
Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome.
Norouzi Rostami F, Sadeghi H, Hashemi-Gorji F, Tehrani Fateh S, Mirfakhraie R, Karimzadeh P, Davarpanah M, Jamshidi S, Madannejad R, Moghimi P, Ekrami M, Miryounesi M, Ghasemi MR. Norouzi Rostami F, et al. Among authors: tehrani fateh s. Heliyon. 2024 Mar 6;10(6):e27434. doi: 10.1016/j.heliyon.2024.e27434. eCollection 2024 Mar 30. Heliyon. 2024. PMID: 38501011 Free PMC article.
The first Iranian patient with You-Hoover-Fong syndrome and a review of the literature on 27 cases: expanding the genotypic and phenotypic spectrum.
Shokrollahi N, Tehrani Fateh S, Nouri M, Behnam A, Moghimi P, Sadeghi H, Mirfakhraie R, Roudgari H, Jamshidi S, Miryounesi M, Ghasemi MR. Shokrollahi N, et al. Among authors: tehrani fateh s. Neurol Sci. 2024 Aug;45(8):3979-3987. doi: 10.1007/s10072-024-07413-y. Epub 2024 Feb 29. Neurol Sci. 2024. PMID: 38421525 Review.
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review.
Ghasemi MR, Tehrani Fateh S, Moeinafshar A, Sadeghi H, Karimzadeh P, Mirfakhraie R, Rezaei M, Hashemi-Gorji F, Rezvani Kashani M, Fazeli Bavandpour F, Bagheri S, Moghimi P, Rostami M, Madannejad R, Roudgari H, Miryounesi M. Ghasemi MR, et al. Among authors: tehrani fateh s. BMC Med Genomics. 2024 Feb 13;17(1):51. doi: 10.1186/s12920-024-01810-0. BMC Med Genomics. 2024. PMID: 38347586 Free PMC article.
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