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Original Article

1. Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum
Sara Taghizadeh ORCID, Raheleh Vazehan, Maryam Beheshtian ORCID, Farnaz Sadeghinia, Zohreh Fattahi, Marzieh Mohseni, Sanaz Arzhangi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi* ORCID, Kimia Kahrizi* ORCID
Arch Iran Med. 2020;23(7): 426-433. doi: 10.34172/aim.2020.39
Scopus ID: 85088097027    
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Original Article

2. Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism
Goli Kazemi ORCID, Fatemeh Peymani, Marzieh Mohseni, Farzane Zare Ashrafi, Sanaz Arzhangi, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Kimia Kahrizi, Hossein Najmabadi* ORCID
Arch Iran Med. 2020;23(12): 842-847. doi: 10.34172/aim.2020.112
Scopus ID: 85097789447    
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2
Original Article

3. The PTRHD1 Mutation in Intellectual Disability

Sara Cheraghi ORCID, Sahar Moghbelinejad, Hossein Najmabadi, Kimia Kahrizi, Reza Najafipour* ORCID
Arch Iran Med. 2021;24(10): 747-751. doi: 10.34172/aim.2021.110
Scopus ID: 85119435694    
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Case Report

4. An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene
Marzieh Mohseni ORCID, Yusuf Mohammadi ORCID, Farzane Zare Ashrafi, Fatemeh Ghodratpour, Khadijeh Jalalvand, Sanaz Arzhangi, Mojgan Babanejad, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi* ORCID
Arch Iran Med. 2023;26(3): 176-180. doi: 10.34172/aim.2023.27
PMCID: PMC10685723     PMID: 37543941     Scopus ID: 85166776646    
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Case Report

5. Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran
Masoumeh Goleyjani Moghadam ORCID, Zohreh Elahi, Mohamad Soveyzi, Sanaz Arzhangi, Shahriar Nafissi, Hossein Najmabadi, Kimia Kahrizi, Zohreh Fattahi* ORCID
Arch Iran Med. 2023;26(5): 279-284. doi: 10.34172/aim.2023.43
PMCID: PMC10685863     PMID: 38301092     Scopus ID: 85171445703    
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Case Report

6. Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII

Amir Hossein Ebrahimi ORCID, Manzar Bolhassani ORCID, Mohammad Reza Zarei ORCID, Matin Heidari ORCID, Amin ArdeshirDavani, Amir Hosein Mehrtash, Zahra Shiri ORCID, Masoud Heidari ORCID, Morteza Soleyman-Nejad, Mohammad Hossein Taskhiri, Arefeh Norouzbeigi, Mansour Heidari* ORCID
Arch Iran Med. 2024;27(4): 223-226. doi: 10.34172/aim.2024.32
PMCID: PMC11097304     PMID: 38685849     Scopus ID: 85191930074    
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Original Article

7. Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière’s Disease
Zohreh Mehrjoo ORCID, Kimia Kahrizi, Marzieh Mohseni, Mojdeh Akbari, Sanaz Arzhangi, Khadijeh Jalalvand, Hossein Najmabadi, Mohammad Farhadi, Mohammad Mohseni, Alimohamad Asghari, Saleh Mohebbi, Ahmad Daneshi* ORCID
Arch Iran Med. 2020;23(5): 319-325. doi: 10.34172/aim.2020.21
Scopus ID: 85084406585    
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Case Report

8. A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4
Farzane Zare Ashrafi ORCID, Saeed Dorgaleleh, Raziye Rezvani Rezvandeh, Negar Kazemi, Nasrin Azizi, Masoud Edizadeh, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi, Reza Najafipour, Marzieh Mohseni* ORCID
Arch Iran Med. 2024;27(9): 522-526. doi: 10.34172/aim.28745
PMCID: PMC11496598     PMID: 39465527     Scopus ID: 85206813812    
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Case Report

9. Pheochromocytoma/Paraganglioma Syndrome Type 1 Presenting with Atypical Symptoms and a Novel Pathogenic Variant in the SDHD Gene: A Case Report
Elham Zohrehvand ORCID, Nastaran Injinari, Maryam Kiani Feyzabadi, Kazem Aghili, Farahnaz Ghaemi, Reyhaneh Azizi* ORCID
Arch Iran Med. 2024;27(8): 447-451. doi: 10.34172/aim.28810
PMCID: PMC11416696     PMID: 39306716     Scopus ID: 85201920706    
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Original Article

10. A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant
Amir Anushiravani ORCID, Hossein Jafari Khamirani ORCID, Ashraf Mohamadkhani, Arya Mani, Mehdi Dianatpour* ORCID, Reza Malekzadeh* ORCID
Arch Iran Med. 2023;26(2): 86-91. doi: 10.34172/aim.2023.14
PMCID: PMC10685898     PMID: 37543928     Scopus ID: 85164787469    
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Original Article

11. Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment
Hoda Mehregan, Marzieh Mohseni, Mojdeh Akbari, Khadijeh Jalalvand, Sanaz Arzhangi, Nooshin Nikzat, Kimia Kahrizi, Hossein Najmabadi*
Arch Iran Med. 2019;22(4): 189-197.
PMID: 31126177     Scopus ID: 85066931504    
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Original Article

12. Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing
Jafar Mehrabi Sisakht ORCID, Maghsood Mehri, Hossein Najmabadi, Azita Azarkeivan, Maryam Neishabury* ORCID
Arch Iran Med. 2022;25(10): 691-697. doi: 10.34172/aim.2022.108
PMCID: PMC10685872     PMID: 37542401     Scopus ID: 85146830006    
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SCImago Journal & Country Rank

About Us

A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.