May 2025, Vol 28, No. 5

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. Screening of Hearing in Newborn Infants: Follow-Up and Outcome After 40930 Births in Babol, Northern Iran

Yadollah Zahed Pasha, Mohammad Zamani*, Ali Hashemi Fard, Ermia Zahed Pasha

Arch Iran Med. 2018;21(9): 382-386.

PMID: 30221527 Scopus ID: 85059581150

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Original Article

2. 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

3. 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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Case Report

4. A Novel Candidate Gene MACF1 is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family

Niloofar Bazazzadegan* , Mojgan Babanejad , Susan Banihashemi, Sanaz Arzhangi, Kimia Kahrizi , Kevin TA Booth , Hossein Najmabadi

Arch Iran Med. 2025;28(1): 63-66. doi: 10.34172/aim.31746

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Case Report

5. Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy

Faezeh Jamali, Hamid Ghaedi, Abbas Tafakhori, Elham Alehabib, Marjan Chapi, Narsis Daftarian, Hossein Darvish*, Javad Jamshidi

Arch Iran Med. 2019;22(12): 728-730.

PMID: 31823625 Scopus ID: 85076339219

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Review Article

6. Expanding the Clinical Phenotype Associated with the NIN Gene; Report of a Patient with Short Stature, Microcephaly and Hearing Loss

Shima Zamanian Najafabadi , Zeinab Ghorbanoghli , Zhila Ghaderi, Fariba Afroozan, Ali Talea, Fatemeh Ahangari, Mina Makvand, Hossein Najmabadi, Ariana Kariminejad*

Arch Iran Med. 2025;28(5): 313-321. doi: 10.34172/aim.33542

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Case Report

7. 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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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.