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Original Article

1. 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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7
Original Article

2. 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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6
7
Original Article

3. 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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Case Report

4. 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    
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Original Article

5. 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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4
2
Original Article

6. 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    
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Case Report

7. 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
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Original Article

8. 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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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.