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Year Number of Results
2012 1
2016 2
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2018 2
2020 1
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2022 8
2023 4
2024 0

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Nejabat M, Naghash P, Dastsooz H, Mohammadi S, Alipour M, Fardaei M. Nejabat M, et al. Among authors: mohammadi s. J Ophthalmic Vis Res. 2018 Apr-Jun;13(2):213. doi: 10.4103/jovr.jovr_52_18. J Ophthalmic Vis Res. 2018. PMID: 29719656 Free PMC article. No abstract available.
Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review.
Ehsani E, Khamirani HJ, Abbasi Z, Gohari M, Zoghi S, Mohammadi S, Dianatpour M, Tabei SMB, Mohamadjani O, Dastgheib SA. Ehsani E, et al. Among authors: mohammadi s. Eur J Med Genet. 2022 Aug;65(8):104552. doi: 10.1016/j.ejmg.2022.104552. Epub 2022 Jun 22. Eur J Med Genet. 2022. PMID: 35752288 Review.
Phenotype of ST3GAL3 deficient patients: A case and review of the literature.
Khamirani HJ, Zoghi S, Faghihi F, Dastgheib SA, Hassanipour H, Bagher Tabei SM, Mohammadi S, Masoudi M, Poorang S, Ehsani E, Dianatpour M. Khamirani HJ, et al. Among authors: mohammadi s. Eur J Med Genet. 2021 Aug;64(8):104250. doi: 10.1016/j.ejmg.2021.104250. Epub 2021 May 20. Eur J Med Genet. 2021. PMID: 34022416 Review.
A novel PTRH2 missense mutation causing IMNEPD: a case report.
Khamirani HJ, Zoghi S, Dianatpour M, Jankhah A, Tabei SS, Mohammadi S, Dastgheib SA. Khamirani HJ, et al. Among authors: mohammadi s. Hum Genome Var. 2021 Jun 10;8(1):23. doi: 10.1038/s41439-021-00147-9. Hum Genome Var. 2021. PMID: 34112751 Free PMC article.
25 results