Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Faculty Members have conducted research related to the A Novel Mutation in the Oxct1 Gene Causing Succinyl-Coa:3-Ketoacid Coa Transferase (Scot) Deficiency Starting With Neurologic Manifestations
Mahdi Zamani
Mahdi Zamani

Professor of Medical Genetics

Department Medical Genetics

School of Medicine

Tehran University of Medical Sciences

All Documents
1. Drug Response of Iranian Alzheimer’S Patients to Rivastigmine Concerning Their Genotype for Vdr Rs11568820 and Mthfr C677t Variants: A Pharmacogenetic and Association Study, Journal of Molecular Neuroscience (2024)
2. Hla-B*51:01 in Iranian Patients With Behcet Uveitis Syndrome; [Hla B51 En Pacientes Iranies Con Uveitis En Contexto De Sindrome De Behcet], Reumatologia Clinica (2024)
3. The Introduction of Basic Fibroblast Growth Factor Promotes Quadriceps Muscle Regeneration After Damage in Mice, Journal of Sciences# Islamic Republic of Iran (2023)
4. The Introduction of Basic Fibroblast Growth Factor Promotes Quadriceps Muscle Regeneration After Damage in Mice, Journal of Sciences, Islamic Republic of Iran (2023)
5. Clinical, Laboratory Data and Outcomes of 17 Iranian Citrullinemia Type 1 Patients: Identification of Five Novel Ass1 Gene Mutations, JIMD Reports (2022)
6. Contribution of Hla Class Ii Genes, Drb4*01:01, Drb1*07:01, and Dqb1*03:03:2 to Clinical Features of Vitiligo Disease in Iranian Population, Molecular Biology Reports (2022)
7. The Impact of the Hla Dqb1 Gene and Amino Acids on the Development of Narcolepsy, International Journal of Neuroscience (2022)
8. Pharmacogenetic and Association Studies on the Influence of Hla Alleles and Rivastigmine on the Iranian Patients With Late-Onset Alzheimer’S Disease, Molecular Neurobiology (2021)
9. Genetic Analysis of Mecp2 Gene in Iranian Patients With Rett Syndrome, Iranian Journal of Child Neurology (2019)
10. Genetic Analysis of Mecp2 Gene in Iranian Patients With Rett Syndrome, Iranian Journal of Child Neurology (2019)
11. Il-7Ra Association and Genotype-Dependent Severity and Response to Ifn-Β Therapy in Multiple Sclerosis, Acta Medica Iranica (2019)
12. Combination of Interleukin-10 Gene Promoter Polymorphisms With Hla-Drb1*15 Allele Is Associated With Multiple Sclerosis, Indian Journal of Medical Research (2017)
13. Pharmacogenetic Study on the Impact of Rivastigmine Concerning Genetic Variants of A2m and Il-6 Genes on Iranian Alzheimer’S Patients, Molecular Neurobiology (2016)
14. Reciprocal 22Q11.2 Deletion and Duplication in Siblings With Karyotypically Normal Parents, Cytogenetic and Genome Research (2016)
15. Reciprocal 22Q11.2 Deletion and Duplication in Siblings With Karyotypically Normal Parents, Cytogenetic and Genome Research (2016)
16. Analysis of Dystrophin Gene in Iranian Duchenne and Becker Muscular Dystrophies Patients and Identification of a Novel Mutation, Neurological Sciences (2015)
17. Association Analysis of Disc1 Gene Polymorphisms With Attention-Deficit Hyperactivity Disorder in Iranian Population, Pakistan Journal of Medical Sciences (2015)
18. Association of Cd58 Polymorphism With Multiple Sclerosis and Response to Interferon ß Therapy in a Subset of Iranian Population, Cell Journal (2015)
19. The Involvement of the Hla-Dqb1 Alleles in the Risk and the Severity of Iranian Coeliac Disease Patients, International Journal of Immunogenetics (2014)
20. Detection of Duchenne/Becker Muscular Dystrophy Carriers in a Group of Iranian Families by Linkage Analysis, Acta Medica Iranica (2011)