November 2024, Vol 27, No. 11

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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Case Report

3. 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

4. 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

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Original Article

5. 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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Original Article

6. 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

7. 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

Scopus ID: 85201920706

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Original Article

8. 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

9. 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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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.