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Works (6)

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

Case Reports in Genetics
2023-08-28 | Journal article
Contributors: Hossein Jalali; Mahan Mahdavi; Mohammad Eslamijouybari; Mohammad Reza Mahdavi; Sofia Priyadarsani Das
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First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy

Clinical Case Reports
2022-08 | Journal article
Contributors: Hossein Jalali; Atefeh Khoshaeen; Mohammad Reza Mahdavi; Mahan Mahdavi
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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

European Journal of Ophthalmology
2021-09 | Journal article
Contributors: Hossein Jalali; Mojtaba Najafi; Atefeh Khoshaeen; Mohammad Reza Mahdavi; Mahan Mahdavi
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Cryptococcal meningoencephalitis in a multiple sclerosis patient after fingolimod discontinuation—a case report

Neurological Sciences
2021-03-24 | Journal article
Contributors: Seyed Mohammad Baghbanian; Mohammad Reza Mahdavi Amiri
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A novel missense mutation (c.1006C>T) of SPG20 gene associated with Troyer syndrome

Journal of Genetics
2020-12 | Journal article
Contributors: A. Khoshaeen; M. Najafi; M. R. Mahdavi; H. Jalali; M. Mahdavi
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Antibacterial Studies on Extracts of Three Species ofGlaucium. from Iran

Journal article
DOI:

10.1080/13880200590928816

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Mohammad Reza Mahdavi