February 2025, Vol 28, No. 2

Journal Metrics

CiteScore (2023): 2.2

SNIP (2020): 0.90

IPP (2020): 1.49

SJR (2023): 0.39

Editor-in-Chief

Professor Reza Malekzadeh

Original Article

1. Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum

Sara Taghizadeh , Raheleh Vazehan, Maryam Beheshtian , Farnaz Sadeghinia, Zohreh Fattahi, Marzieh Mohseni, Sanaz Arzhangi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi* , Kimia Kahrizi*

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 , Fatemeh Peymani, Marzieh Mohseni, Farzane Zare Ashrafi, Sanaz Arzhangi, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2020;23(12): 842-847. doi: 10.34172/aim.2020.112

Scopus ID: 85097789447

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Original Article

3. The PTRHD1 Mutation in Intellectual Disability

Sara Cheraghi , Sahar Moghbelinejad, Hossein Najmabadi, Kimia Kahrizi, Reza Najafipour*

Arch Iran Med. 2021;24(10): 747-751. doi: 10.34172/aim.2021.110

Scopus ID: 85119435694

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Case Report

4. Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran

Masoumeh Goleyjani Moghadam , Zohreh Elahi, Mohamad Soveyzi, Sanaz Arzhangi, Shahriar Nafissi, Hossein Najmabadi, Kimia Kahrizi, Zohreh Fattahi*

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

5. An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene

Marzieh Mohseni , Yusuf Mohammadi , Farzane Zare Ashrafi, Fatemeh Ghodratpour, Khadijeh Jalalvand, Sanaz Arzhangi, Mojgan Babanejad, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi*

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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Original Article

6. A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant

Amir Anushiravani , Hossein Jafari Khamirani , Ashraf Mohamadkhani, Arya Mani, Mehdi Dianatpour* , Reza Malekzadeh*

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

7. Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière’s Disease

Zohreh Mehrjoo , Kimia Kahrizi, Marzieh Mohseni, Mojdeh Akbari, Sanaz Arzhangi, Khadijeh Jalalvand, Hossein Najmabadi, Mohammad Farhadi, Mohammad Mohseni, Alimohamad Asghari, Saleh Mohebbi, Ahmad Daneshi*

Arch Iran Med. 2020;23(5): 319-325. doi: 10.34172/aim.2020.21

Scopus ID: 85084406585

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Case Report

8. Pheochromocytoma/Paraganglioma Syndrome Type 1 Presenting with Atypical Symptoms and a Novel Pathogenic Variant in the SDHD Gene: A Case Report

Elham Zohrehvand , Nastaran Injinari, Maryam Kiani Feyzabadi, Kazem Aghili, Farahnaz Ghaemi, Reyhaneh Azizi*

Arch Iran Med. 2024;27(8): 447-451. doi: 10.34172/aim.28810

PMCID: PMC11416696 PMID: 39306716 Scopus ID: 85201920706

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Case Report

9. A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4

Farzane Zare Ashrafi , Saeed Dorgaleleh, Raziye Rezvani Rezvandeh, Negar Kazemi, Nasrin Azizi, Masoud Edizadeh, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi, Reza Najafipour, Marzieh Mohseni*

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

10. First Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants

Azadeh Reshadmanesh , Shima Dehdahsi , Fatemeh Ahangari, Kimia Kahrizi, Ariana Kariminejad, Shokouh Sadat Mahdavi, Saeed Talebi* , Hossein Najmabadi*

Arch Iran Med. 2024;27(12): 700-706. doi: 10.34172/aim.31593

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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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Case Report

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

Amir Hossein Ebrahimi , Manzar Bolhassani , Mohammad Reza Zarei , Matin Heidari , Amin ArdeshirDavani, Amir Hosein Mehrtash, Zahra Shiri , Masoud Heidari , Morteza Soleyman-Nejad, Mohammad Hossein Taskhiri, Arefeh Norouzbeigi, Mansour Heidari*

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

13. Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing

Jafar Mehrabi Sisakht , Maghsood Mehri, Hossein Najmabadi, Azita Azarkeivan, Maryam Neishabury*

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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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.