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Year | Number of Results |
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2020 | 1 |
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Page 1
Improved biological behaviours and osteoinductive capacity of the gelatin nanofibers while composites with GO/MgO.
Cell Biochem Funct. 2022 Mar;40(2):189-198. doi: 10.1002/cbf.3688. Epub 2022 Feb 3.
Cell Biochem Funct. 2022.
PMID: 35118692
First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy.
Jalali H, Khoshaeen A, Mahdavi MR, Mahdavi M.
Jalali H, et al. Among authors: mahdavi m.
Clin Case Rep. 2022 Aug 9;10(8):e6203. doi: 10.1002/ccr3.6203. eCollection 2022 Aug.
Clin Case Rep. 2022.
PMID: 35957775
Free PMC article.
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Coinheritance of the c.-19 G > C and c.315 + 1 G > A Variants in the β-Globin Gene Leads to Thalassemia Disease: A Report from the North of Iran.
Jalali H, Mahdavi M, Eslamijouybari M, Mahdavi MR.
Jalali H, et al. Among authors: mahdavi m.
Case Rep Genet. 2023 Aug 28;2023:9950421. doi: 10.1155/2023/9950421. eCollection 2023.
Case Rep Genet. 2023.
PMID: 37671080
Free PMC article.
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First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia.
Jalali H, Najafi M, Khoshaeen A, Mahdavi MR, Mahdavi M.
Jalali H, et al. Among authors: mahdavi m.
Eur J Ophthalmol. 2021 Sep;31(5):NP23-NP26. doi: 10.1177/1120672120921734. Epub 2020 May 17.
Eur J Ophthalmol. 2021.
PMID: 32418451
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