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Mohammad Reza Mahdavi

Observed names: M R Mahdavi, M. Mahdavi, M. R. Mahdavi, Mahdavi M.R., Mahdavi MR, Mahdavi Mr, Mohammad Reza Mahdavi Amiri
ORCID: 0000-0002-1453-5570
Observed ORCID: 0000-0002-1453-5570
OpenAlex ID: A5100690237
Protective role of Pleurotus porrigens (Angel's wings) against gentamicin-induced nephrotoxicty in mice.
2010 · A Hajizadeh Moghaddam, M Javaheri, et al. · PubMed · 21
Hepatitis C prevalence studied by polymerase chain reaction and serological methods in haemodialysis patients in Mazandaran, Iran.
2008 · A Makhlough, M Jamshidi, et al. · PubMed · 21
Antibacterial Studies on Extracts of Three Species ofGlaucium. from Iran
2005 · Katayoun Morteza-Semnani, Madjid Saeedi, et al. · Pharmaceutical Biology · 15
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Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening
2013 · Mohammad Reza Mahdavi, Hosein Karami, et al. · Case Reports in Hematology · 12
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Hepatitis B vaccination status in health-care workers.
2005 · M J Saffar, A R Jooyan, et al. · PubMed · 9
First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy
2022 · Hossein Jalali, Atefeh Khoshaeen, et al. · Clinical Case Reports · 6
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Cryptococcal meningoencephalitis in a multiple sclerosis patient after fingolimod discontinuation—a case report
2020 · Seyed Mohammad Baghbanian, Mohammad Reza Mahdavi Amiri · Neurological Sciences · 6
A Review on Thalassemia and Related Complications
2013 · Mohammad Reza Mahdavi, Mohammad Taher Hojjati, et al. · Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Māzandarān/Journal of Mazandaran University of Medical Sciences · 6
First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia
2020 · Hossein Jalali, Mojtaba Najafi, et al. · European Journal of Ophthalmology · 4
Role of C-reactive Protein and Tumor Necrosis Factor-Alpha in Differentiating between Ventilator-Associated Pneumonia and Systemic Inflammatory Response Syndrome without Infectious Etiology.
2016 · Ebrahim Salehifar, Shima Tavakolian Arjmand, et al. · PubMed · 4
Neonatal Screening for G6PD Deficiency in Mazandaran Province, Iran 2007-2010
2011 · Mehrnoush Kosaryan, Mohammad Nasehi, et al. · 4
Comparison of hepatitis C virus genotypes in hemodialysis and nonuremic patients
2010 · Atiyeh Makhloogh, N. Aezinia, et al. · 4
A novel missense mutation (c.1006C>T) of SPG20 gene associated with Troyer syndrome
2020 · A. Khoshaeen, M. Najafi, et al. · Journal of Genetics · 2
Co-Inheritance of Heterozygous β0-Thalassemia with Single Functional α-Globin Gene: Challenges of Carrier Detection in Pre-Marital Screening Program for Thalassemia
2022 · Hossein Jalali, Hossein Karami, et al. · Thalassemia Reports · 1
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Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene
2022 · Hossein Jalali, Mohammad Reza Mahdavi, et al. · Thalassemia Reports · 1
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Is Quantitative HBsAg Measurement a Reliable Substitute for HBV DNA Quantitation
2015 · Mohammad Reza Mahdavi, Mohammad Reza Haghshenas, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 1
A new frame shift pathogenic variant (c.773dupT) in the BCKDHB gene caused MSUD in an infant from north of Iran
2026 · Hossein Jalali, Daniel Zamanfar, et al. · Case Reports in Perinatal Medicine
Identification of a Novel GNAI1 Variant (c.593T>A) Associated With Neurodevelopmental Disorder in an Iranian Family
2025 · Hossein Jalali, Mousa Rajabi, et al. · Research in Molecular Medicine
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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
2023 · Hossein Jalali, Mahan Mahdavi, et al. · Case Reports in Genetics
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Hemoglobin Daneshgah-Tehran (HBA1:c.218A>G p.His72Arg): a Rare α1-Globin Variant from Iran
2020 · Hossein Jalali, Mohammad Reza Mahdavi, et al. · Iranian Journal of Pediatric Hematology & Oncology
Identification of a Neonate with Intermediate Thalassemia Despite Premarital Screening Program in Mazandaran Province (Co Inheritance of Hb Knossos and IVS II-1 G> A Mutations)
2017 · Hossein Karami, Hossein Jalali, et al. · Research in Molecular Medicine
Carrier frequency of alpha thalassemia mutations among newborns in northern Iran
2016 · Mahdavi Mr, Mehrnoush Kosaryan, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Comparison of fluorescent spot test, decolorization test and quantitative enzyme assay in detection of G6PD enzyme deficiency
2015 · Kosaryan M, Mahdavi MR, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Molecular detection of mutations causing drug resistance mycobacterium tuberculosis strains among patients with tuberculosis in Mazandaran
2015 · Mehrdad Mahdavi, Mohammad Reza Mahdavi, et al.
Beta globin gene haplotypes associated with hemoglobin D-Punjab in northern Iran
2015 · Jalali H, Mahdavi MR, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Works count: 35
Citation count: 121
H-index: 6
I10-index: 4
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