1. 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

Article

PDF

XML

Cited By:

Review

2. Contribution of Iran in Elucidating the Genetic Causes of Autosomal Recessive Intellectual Disability

Reza Ataei, Shahrouz Khoshbakht, Maryam Beheshtian, Seyedeh Sedigheh Abedini, Hanieh Behravan, Saeed Esmaeili Dizghandi, Fatemeh Godratpour, Sepide Mirzaei, Fatemeh Bahrami, Mojdeh Akbari, Fatemeh Keshavarzi, Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2019;22(8): 461-471.

PMID: 31679349 Scopus ID: 85074416936

Article

PDF

XML

Cited By:

Original Article

3. 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

Article

PDF

XML

Cited By:

Submit Your Paper Notification Instructions for Authors Aims and Scope Editorial policies Editorial Board AIM old site Archive

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.